Recent progress in engineering the genomes of large animals has spurred increased interest in developing better animal models for diseases where current options are inadequate. Here, we report the creation of Yucatan miniature pigs with targeted disruptions of the low-density lipoprotein receptor (LDLR) gene in an effort to provide an improved large animal model of familial hypercholesterolemia and atherosclerosis. Yucatan miniature pigs are well established as translational research models because of similarities to humans in physiology, anatomy, genetics, and size. Using recombinant adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer, male and female LDLR+/− pigs were generated. Subsequent breeding of heterozygotes produced LDLR−/− pigs. When fed a standard swine diet (low fat, no cholesterol), LDLR+/− pigs exhibited a moderate, but consistent increase in total and LDL cholesterol, while LDLR−/− pigs had considerably elevated levels. This severe hypercholesterolemia in homozygote animals resulted in atherosclerotic lesions in the coronary arteries and abdominal aorta that resemble human atherosclerosis. These phenotypes were more severe and developed over a shorter time when fed a diet containing natural sources of fat and cholesterol. LDLR-targeted Yucatan miniature pigs offer several advantages over existing large animal models including size, consistency, availability, and versatility. This new model of cardiovascular disease could be an important resource for developing and testing novel detection and treatment strategies for coronary and aortic atherosclerosis and its complications.
Citation: Davis BT, Wang X-J, Rohret JA, Struzynski JT, Merricks EP, Bellinger DA, et al. (2014) Targeted Disruption of LDLR Causes Hypercholesterolemia and Atherosclerosis in Yucatan Miniature Pigs. PLoS ONE 9(4): e93457. doi:10.1371/journal.pone.0093457
Editor: Yanqiao Zhang, Northeast Ohio Medical University, United States of America
Received: February 6, 2014; Accepted: March 5, 2014; Published: April 1, 2014
Copyright: © 2014 Davis et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was funded by a grant from the National Heart, Lung, and Blood Institute of the National Institutes of Health (HL102950). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: BTD, XJW, JAR, JTS, FAR and CSR are employees of Exemplar Genetics, a company that has applied for a patent and intends to commercialize the porcine models described. BTD, XJW, JAR, JTS, FAR and CSR are employees of Exemplar Genetics, a company that has applied for a patent and intends to commercialize the porcine models described. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
The application of gene targeting technology in livestock animals, particularly pigs, has generated significant interest in the development of new models of human diseases. In cases where existing rodent models fail to recreate key clinical phenotypes, pigs are an attractive alternative. Perhaps the best example of this is the recent development of porcine models of cystic fibrosis (CF) , . Pigs expressing either null alleles or the common F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene closely recapitulate human CF, including lung disease , . These models have been important in elucidating new pathogenic mechanisms and uncovering previously unrecognized consequences of the disease; advances that were not possible in prior models of CF , . Pigs also offer an advantage when modeling diseases for which size is relevant to the development of interventional devices and diagnostic equipment for humans, such as atherosclerosis .
Atherosclerosis is characterized by the accumulation of proliferative smooth muscle cells, macrophages, lipids, cholesterol, calcium deposits, and cellular debris in vessel walls –. Atherosclerosis begins with the buildup of low-density lipoprotein (LDL) in the subendothelial matrix . This accumulation is proportional to the levels of circulating LDL. These processes result in plaque formation, arterial obstruction, and diminished blood flow to organs. For unknown reasons, these plaques can rupture, often when quite small, and lead to occlusive thrombosis, resulting in myocardial infarction or stroke –.
In humans, loss-of-function mutations in the LDL receptor (LDLR) gene lead to familial hypercholesterolemia (FH) . As its name implies, FH is associated with elevated plasma concentrations of total and LDL cholesterol. Approximately one in 500 people carries a mutation in one LDLR gene. These heterozygotes typically have twice the normal plasma LDL levels and a significantly increased risk for atherosclerosis. Individuals with two defective LDLR alleles face early-onset atherosclerosis and often die of the disease at a young age.
Several small and large animal models of hypercholesterolemia and atherosclerosis are available today, but each has limited utility. Murine models of atherosclerosis have been developed using transgenic and gene targeting techniques –. While these models have provided valuable insight into our current understanding of cardiovascular disease, differences between murine atherosclerosis and the corresponding human disease have hampered translation to the clinic . For example, atherosclerosis in mice develops above the aortic valve and progresses in an antegrade fashion. Abdominal aortic atherosclerosis in humans begins at the aortoiliac junction and progresses in a retrograde fashion . Also, mice typically do not develop coronary artery atherosclerosis except in the most proximal regions, and these lesions appear to be a direct extension of supra-aortic valve atherosclerosis as opposed to developing separately in the coronary arteries. In contrast, humans develop disease throughout the coronary artery system. Another key limitation of the murine models is size - the small size of the mouse limits their use in the development of human devices (such as stents) and new imaging technologies. Rabbit models of atherosclerosis have also been studied extensively . While they do present a more accurate model of human atherosclerosis, like mice, their smaller size limits their broad application.
Pigs have long been studied as models of human cardiovascular disease, primarily due to similarities of their cardiovascular systems and their more human-like size . For this reason, the pig is a preferred animal for testing in the cardiovascular device industry , . Spontaneous atherosclerosis in pigs is rare, but when fed a diet high in saturated fat and cholesterol, pigs can develop advanced atherosclerotic lesions similar in type and location to those seen in humans –. However, these diets are incredibly expensive and require a long time to manifest disease, making many studies cost-prohibitive.
Pigs with spontaneous hypercholesterolemia and FH have been described by Rapacz and others –. These pigs harbor a point mutation (R84C) in both LDLR alleles that reduces receptor binding, as well as allele variations in ApoB that may further contribute to the phenotype. Even when consuming a normal diet, these pigs develop hypercholesterolemia and atherosclerotic lesions ranging from fatty streaks to advanced plaques, with accompanying calcification, neovascularization, hemorrhage, and rupture . Despite the promising phenotype, there are significant drawbacks to the Rapacz FH pig. First, there is substantial variability in the plasma cholesterol levels and disease development . This is likely due to the mild nature of the mutation and the broad genetic background of these animals. Second, the mutations were originally described in a large domestic pig breed, with body weights in excess of 200 kg. Efforts to downsize the pig by crossing with various miniature pig breeds has resulted in smaller pigs, but has also led to greater phenotypic variability .
Recently, the development of transgenic Yucatan miniature pigs expressing a proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation (D374Y), which is associated with human autosomal dominant FH, was reported . These pigs exhibit moderate hypercholesterolemia on standard pig feed, and a more severe hypercholesterolemia and human-like atherosclerosis following extended feeding of a high-fat, high cholesterol diet. However, with the mutant transgene being permanently overexpressed at nearly 500 times the normal level (hepatic mRNA expression), these pigs may have limited utility for treatments designed to increase LDL receptor expression or reduce PCSK9 activity.
We endeavored to address the disadvantages of the current models while maintaining the positive attributes of pigs in accurately modeling human cardiovascular disease. We used gene targeting and somatic cell nuclear transfer (SCNT) to create Yucatan miniature pigs with targeted disruptions in one or both LDLR alleles. We also evaluated the extent of hypercholesterolemia and atherosclerosis with both standard and high fat, high cholesterol diets.
This study was carried out in accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The Institutional Animal Care and Use Committee of Exemplar Genetics approved all animal experiments. All animals were housed in Exemplar Genetics' AAALAC-accredited facilities. Standard procedures for animal husbandry were used throughout.
Fetal Fibroblast Isolation
Fetal fibroblasts were previously isolated from approximately day 35 Yucatan miniature pig fetuses as previously described . Fetus genders were identified by PCR amplification of the Y-chromosome-specific Sry gene .
Cloning porcine LDLR genomic DNA
Genomic DNA was isolated from Yucatan fetal fibroblasts (Qiagen). A 8.6 kb PCR product which included a region from LDLR exon 2 to exon 6 was amplified using a high fidelity polymerase (Platinum Taq High Fidelity; Invitrogen) and LDLR primers 2F2 and 6R2 (see Table S1 for primer sequences). The PCR product was subcloned into pCR2.1-TOPO (Invitrogen) and sequenced. All DNA sequencing was performed by the University of Iowa DNA Facility. This plasmid (referred to as pLDLR2/6) served as the template for PCR amplification of the 5′ and 3′ homologous targeting arms.
Targeting Vector Construction
The 5′ and 3′ homology arms were amplified by PCR using plasmid pLDLR2/6 and subcloned sequentially into a plasmid containing a PGK-NeoR cassette. The primers for the 5′ arm were LDLR5′armF (XhoI) and LDLR5′armR (EcoRV). The primers for the 3′ arm were LDLR3′armF (HindIII) and LDLR3′armR (HindIII). The engineered termination codon is at amino acid position C128 (C128X). This targeting construct (pLDLR-Neo) was used as a template to create the amplicon for the generation of the LDLR-targeting proviral vector.
PCR amplification of a 4.5 kb amplicon from plasmid pLDLR-Neo was achieved by using the following primers: AAV-LDLR-F (NotI) and AAV-LDLR-R (NotI). This product was subcloned into the rAAV proviral plasmid, pFBAAV2-CMVP.NpA (obtained from University of Iowa Gene Transfer Vector Core) and grown in Sure2 cells (Stratagene) to ensure ITR integrity. This proviral plasmid is referred to as pAAV-LDLR-Neo. The rAAV targeting virus was produced by the University of Iowa Gene Transfer Vector Core.
Fetal fibroblast infection, selection, and screening
rAAV infection, antibiotic selection, and PCR screening (using primers LDLR Ex4aF1 and LDLR Int4R1) were performed as previously described . The expected PCR screening product for the wild-type allele was 1.5-kb and 3.2-kb product from the LDLR-targeted allele.
Genomic DNA isolation, whole genome amplification, and Southern blotting procedures were performed as previously described . The DNA probes for LDLR and NeoR were produced by PCR amplification using the following primers: LDLR XmnI probe1F/LDLR XmnI probe 1R and PGK-NeoF/NeoR-R, respectively.
Production of pigs by SCNT
Nuclear transfer was performed by Viagen, Inc. (Austin, TX) as previously described . Reconstructed oocytes were transferred into synchronized post-pubertal gilts on the first day of standing estrus. Following a midline incision to access the uterus, reconstructed embryos were transferred into the oviduct at the ampullary-isthmus junction. Recipient animals were checked for pregnancy by abdominal ultrasound after day 21 and throughout gestation.
Total RNA was isolated (RNaqueous-4 PCR; Ambion) from LDLR+/+, LDLR+/−, and LDLR−/− pig liver. Poly A+ RNA was obtained from liver total RNA by using FastTrack MAG mRNA Isolation Kits (Invitrogen). Northern blot analysis was performed using the NorthernMax formaldehyde-based system (Ambion). LDLR and GAPDH probe templates were amplified using the primer sets LDLR North8F/9R and pGAPDH North1F/2R, respectively.
Reverse Transcription PCR
Total RNA was isolated as described above. First strand cDNA was synthesized with 2 μg of total RNA using SuperScript III (Invitrogen) and following manufacturer's instructions. PCR was performed using primers LDLR North4F and LDLR Exon 5R1, which spans LDLR exons 1–5.
Pig liver was homogenized on ice in RIPA buffer (1% NP-40, 1% Na-deoxycholate, 0.1% SDS, 0.15 M NaCl, 0.01 M NaPO4 pH 8.0, 2 mM EDTA) supplemented with protease inhibitor cocktail (Sigma), 1 mM PMSF (Sigma), and 1 mM DTT. The homogenate was centrifuged at 4°C, 10,000×g for 30 minutes, and the supernatant was combined with SDS-PAGE sample buffer (50 mM Tris-HCl pH 6.8, 2% SDS, 10% glycerol, 100 mM DTT, 0.1% bromophenol blue). The liver lysate samples were heated in boiling water for 5 minutes, cooled on ice, and sonicated with a Sonic Dismembrator (Fisher Scientific). The samples were electrophoresed in a 7.5% SDS-PAGE gel with Tris-Glycine running buffer. Protein was transferred onto a PVDF Immobilon-P Transfer Membrane (Millipore) using XCell II Blot Module (Invitrogen) according to manufacturer's instructions. Immunoblot analysis was performed using primary antibodies against LDLR (EP1553Y, Abcam), β–tubulin (SC-55529, Santa Cruz Biotechnology), and secondary antibodies conjugated with horseradish peroxidase (SC-2317 and SC-2005, Santa Cruz Biotechnology). Signal was detected using Chemiluminescent Detection Kit (Pierce).
Whole blood was collected in EDTA-containing tubes, and plasma was prepared and frozen at −80°C. Lipid analysis of most samples was performed by the Lipoprotein Analysis Laboratory in the Department of Pathology at Wake Forest University School of Medicine (Winston-Salem, NC). Total cholesterol was measured by enzymatic assay, lipoproteins were measured by gel filtration chromatography. Total cholesterol of samples from 15–18 month old heterozygote animals was determined by LipoScience (Raleigh, NC).
Atherosclerosis measurements and morphometric analysis
The heart and coronary arteries from female LDLR+/+ and LDLR−/− littermates were flushed with normal saline and perfusion-fixed under systemic pressure with 10% buffered formalin. Abdominal aortas were immersion-fixed in 10% buffered formalin. Sections of each coronary artery were taken perpendicular to the direction of blood flow at one cm intervals from their origin and embedded in paraffin. The number of sections reflects the distance covered. In general there are an average of 20 total coronary artery sections per pig heart: 7 left anterior descending coronary artery, 10 right coronary artery, 3 to 4 circumflex. The coronary artery sections were stained with Verhoeff-van Gieson to highlight the internal and external elastic lamina. Adjacent sections were stained with hematoxylin and eosin to confirm lesion details. The abdominal aorta between the renal and iliac arteries was photographed for measuring the percent surface area with raised lesions when macroscopically present as follows: % surface area with raised lesions = (area with raised lesions ÷ total surface area) ×100. Measurements were confirmed by Sudan IV staining. The abdominal aorta was then divided into 1 cm sized opened segments taken perpendicular to the direction of blood flow from the level of the renal arteries to the origin of the iliac arteries, producing on average 6 sections per pig and paraffin embedded. Light microscopic sections were prepared from the proximal half of each segment and stained with Verhoeff-van Gieson and hematoxylin and eosin.
Analysis for significance was performed with GraphPad Prism software (GraphPad Software) using one-way ANOVA with post hoc comparison using the Tukey test or unpaired Student's t test, as specified.
Targeted disruption of porcine LDLR
Homologous recombination was used to disrupt the porcine LDLR gene. Specifically, a neomycin-resistance cassette (NeoR) was inserted into exon 4 of porcine LDLR (Figure 1A). Exon 4 encodes a necessary portion of the LDL receptor's ligand-binding domain . It is a frequent site of mutation in human FH and was also targeted in a murine model, resulting in the loss of LDL receptor function . Additionally, a premature termination codon was engineered immediately upstream of the NeoR insertion to ensure that no functional protein was produced.
A. Gene targeting strategy. Wild-type LDLR exons 2–6 are shown as gray boxes. NeoR cassette is depicted in red, with the arrow showing the orientation relative to LDLR. The neomycin resistance cDNA is driven by a PGK promoter and flanked by loxP sites. The engineered termination codon is indicated. Position of the LDLR Southern blot probe is shown, as are the XmnI restriction sites. B. LDLR+/− piglets at 2 days of age. C. Southern blot of genomic DNA from LDLR+/− cloned pigs. (Upper) XmnI digested genomic DNA was hybridized with a probe that detects porcine LDLR downstream of the targeting vector boundary. The LDLR-targeted allele produced an approximately 7.8 kb band, and the wild-type band is approximately 6.0 kb. (Lower) The same DNA was hybridized with a probe that detects the NeoR cassette, yielding only the targeted 7.8 kb band. Lanes 1–5 contain DNA from individual cloned LDLR+/− pigs; lane 6 contains DNA from a wild-type pig. D. Sequence chromatogram of the site of LDLR disruption by the NeoR cassette. The engineered termination codon is noted. E. Total cholesterol levels in plasma from 15–18 month old LDLR+/− pigs (n = 13) and wild-type controls (n = 7), *p<0.0001. Data presented with SD.
Recombinant adeno-associated virus (rAAV) was used to deliver the targeting vector to male and female fibroblasts harvested from Yucatan miniature pig fetuses. Following rAAV infection and antibiotic selection, LDLR-targeted fibroblasts were identified using PCR (Figure S1A). The gene targeting efficiency (1.8% in male cells and 6.5% in female cells) was comparable to other studies using rAAV to target porcine genes (Table 1) , . Several PCR-positive cell lines were further confirmed by Southern blot analysis to contain the expected LDLR targeting event and were free of random integration (Figure S1B).
Generation of LDLR+/− pigs by SCNT
LDLR+/− cells were used as nuclear donors for SCNT . We performed 18 embryo transfers yielding 9 full term pregnancies and 57 LDLR+/− piglets (24 male and 33 female) (Figure 1B). Southern blot and DNA sequencing confirmed the expected genotypes (Figure 1C,D).
Naturally occurring FH pigs have previously been shown to inherit the disease in a recessive manner with heterozygotes displaying no significant elevation in total cholesterol . To assess whether this was true in LDLR-targeted Yucatan miniature pigs, total cholesterol was measured in a group of 15 to 18 month old male LDLR+/− cloned pigs (n = 16) and wild-type controls (n = 7) fed a standard diet (~2% fat and no cholesterol). LDLR+/− pigs total cholesterol was elevated relative to control pigs (LDLR+/+: 57.3±4.0 and LDLR+/−: 92.4±5.6, p<0.0001) (Figure 1E).
Production of LDLR−/− pigs by breeding
Cloned LDLR+/− males and females were retained for breeding purposes. For this study, sixteen litters were produced and yielded the expected Mendelian inheritance of 20 LDLR+/+, 40 LDLR+/−, and 21 LDLR−/− pigs. Since the sires and dams were each derived via SCNT from single, LDLR-targeting events, each litter produced from these matings is essentially from the same cross.
Figure 2A,B shows representative genotyping results via PCR and Southern blot. As mentioned previously, we disrupted exon 4 with a NeoR cassette and inserted a premature termination codon. The most likely consequence of this mutation is the induction of nonsense-mediated mRNA decay . However, should a protein be translated, it would be truncated in the ligand-binding domain, lack the transmembrane-spanning segment, and be non-functional . An additional possibility could be the skipping of exon 4 via nonsense-associated altered splicing . This, too, would result in a protein with no ability to bind LDL. Northern blot analysis of liver mRNA suggests that the targeted allele produces no normal LDLR transcripts (Figure 2C), and RT-PCR reveals the presence of truncated mRNAs resulting from transcripts lacking exon 4 as well as exons 3 and 4 (Figure 2D), each a scenario which should result in a frameshift mutation. DNA sequencing confirmed these results (data not shown). Finally, we evaluated all three genotypes for the presence of LDL receptor protein in the liver, which is the primary site of LDLR expression. Western blots confirmed that LDLR−/− pigs produce no normal LDL receptor protein (Figure 2E).
A. Genotyping by PCR. Expected sizes are 1.5-type LDLR and 3.2 kb for targeted LDLR. B. Southern blot of genomic DNA. (Left) XmnI digested genomic DNA was hybridized with a probe that detects porcine LDLR downstream of the targeting vector boundary. The LDLR-targeted allele produced an approximately 7.8 kb band, and the wild-type band is approximately 6.0 kb. (Right) The same DNA was hybridized with a probe that detects the NeoR cassette, yielding only the targeted 7.8 kb band. C. Northern blot of LDLR and GAPDH mRNA. Full-length LDLR and GAPDH mRNAs are 5.1 and 1.5 kb, respectively. The asterisk represents a minor mRNA species consisting of full-length LDLR mRNA plus the NeoR cassette. The bracket indicates two minor mRNA species that are likely the result of nonsense-mediated mRNA altered splicing. D. Representative RT-PCR. Using PCR primers that amplify from exon 1 to exon 5, the targeted LDLR allele produces no normal mRNA, but does produce mRNA species with deletions of exon 4 or exons 3 and 4. This is seen in both the LDLR+/− and LDLR−/− pigs. This result was confirmed by DNA sequencing. E. Representative western blot of LDLR and β-tubulin. LDLR is ~150 kDa and β-tubulin is 51 kDa.
Lipid chemistry analysis
Plasma cholesterol levels were measured in LDLR+/+, LDLR+/−, and LDLR−/− piglets immediately at birth, before piglets could suckle. This allows an initial assessment before lipid levels are affected by the sow's cholesterol- and fat-rich colostrum and milk. As expected, cholesterol levels were significantly higher in LDLR-targeted pigs than in their wild-type littermates. LDLR+/− piglets exhibited a moderate, but statistically significant total cholesterol elevation (similar to what was seen in LDLR+/− male clones described above), while LDLR−/− pigs had dramatically elevated levels (Table 2). A similar elevation is seen in LDL and very low-density lipoprotein (VLDL). High-density lipoprotein (HDL) was decreased in LDLR−/− pigs, though not in LDLR+/− pigs.
Cholesterol levels in pigs can vary widely while nursing (data not shown). At three to four weeks of age, pigs were weaned and placed on a standard diet consisting of no cholesterol and ~2% fat. When measured again at 26 weeks of age, the cholesterol levels in these pigs were similar to what was seen pre-suckle. These cholesterol data are summarized in Table 2.
Early atherosclerosis in LDLR−/− pigs
It is well established that elevated total and LDL cholesterol due to dietary manipulation will lead to the development of atherosclerosis in wild-type pigs. We asked whether LDLR−/− pigs would show the presence of atherosclerosis having been fed a standard pig diet with no added cholesterol or fat. We necropsied three LDLR−/− pigs and two LDLR+/+ controls at 7 months of age and assessed the presence of atherosclerosis in the coronary arteries and the abdominal aorta. The LDLR+/+ pigs had no visible atherosclerosis in the abdominal aorta, while the LDLR−/− pigs had 45% of the abdominal aorta covered with raised atherosclerotic lesions that were distributed fairly equally over proximal and distal portions. Atherosclerotic lesions had areas of probable foam cells and small areas of necrosis, hallmarks of human atherosclerosis (Figure 3A–E).
Measurements of percent surface area with raised lesion in the abdominal aorta were taken from en face photographs of the abdominal aorta and confirmed by Sudan IV staining (A). Aortic sections (rectangle) were stained with VVG and H&E (B,C), higher magnifications of atherosclerotic lesion (squares) are seen in D and E. A representative section (with corresponding higher magnification) from the circumflex artery showing atherosclerotic plaque that appears to have foam cells. (F,G–H&E H,I – VVG).
Coronary arteries from the LDLR+/+ and LDLR−/− pigs were sectioned and stained with hemotoxylin and eosin (H&E) and Verhoeff-van Gieson (VVG) and evaluated for the presence of atherosclerosis. The LDLR+/+ pigs had no visible atherosclerotic lesions in the right coronary artery (RCA), left anterior descending artery (LAD), or circumflex artery (CIRC). Small areas of intimal thickening were seen in the proximal portion of each. The LDLR−/− pigs however, had small atherosclerotic lesions, as well as intimal thickening in sections from the RCA, LAD, and CIRC. These were predominantly in the proximal portion of the arteries but there was some extension into the distal portions as well. A representative lesion is shown in Figure 3F–I. Lesions in the coronary arteries appear to have foam cells, a hallmark of human atherosclerosis.
High fat, high cholesterol diet accelerates atherosclerosis
We next sought to increase the severity and accelerate the onset of atherosclerosis in the LDLR-targeted pigs by feeding a high fat, high cholesterol diet. For this study, we included only females and barrows (castrated males) since they are commonly used for atherosclerosis studies in industry settings. All pigs were raised on a standard diet until the age of 5 months, at which time they were transitioned to a diet containing ~40% saturated fat and ~1% cholesterol from natural sources including eggs and butter.
Cholesterol levels were measured following 90 and 180 days on the diet (Table 3). There was no difference in total cholesterol between females and barrows, so they have been combined within each genotype for this study. After 90 days of ingesting the high fat, high cholesterol diet, all three genotypes experienced significant increases in total cholesterol, which continued to increase at the 180-day time point.
The LDLR−/− pigs had an appreciable amount of atherosclerosis in the abdominal aorta. While the total abdominal aortic surface area was comparable in all three groups, LDLR−/− pigs had significantly higher surface area with raised lesions and percent aortic surface area covered with lesions (overall and in both the proximal and distal portions) than either the LDLR+/− or LDLR+/+ pigs (Figure 4, Table 4). By morphometric methods, the intimal area and intimal area as percent of medial area were also significantly larger (overall and in both the proximal and distal portions) in the LDLR−/− pigs than either the LDLR+/− or LDLR+/+ pigs (Table 4). All aortic atherosclerosis lesions from the LDLR−/− pigs had cholesterol clefts present and many had calcification and apparent foam cells (Figure 4).
Measurements of percent surface area with raised lesion in the abdominal aorta were taken from en face photographs of the abdominal aorta and confirmed by Sudan IV staining (A,D,G). Aortic sections (rectangles) were stained with H&E (B, E, H) and higher magnifications of atherosclerotic lesion (squares) are seen in C, F, and I. Representative sections from each are shown: LDLR−/− (A,B,C), LDLR +/− (D,E,F), and LDLR +/+ (G,H,I). Atherosclerotic plaques from all the LDLR−/− pigs had cholesterol clefts and some lesions also exhibited calcification as shown in B and C.
After 180 days of the high fat, high cholesterol diet, coronary arteries from the 11-month old LDLR+/+, LDLR+/−, and LDLR−/− pigs were sectioned and stained with H&E and VVG and evaluated for the presence of atherosclerosis. The LDLR+/+ pigs had only minimal amounts of intimal thickening in the RCA, LAD, and CIRC, while LDLR+/− pigs had small areas of atherosclerosis in addition to areas of intimal thickening. The LDLR−/− pigs however, had atherosclerotic lesions, as well as intimal thickening in sections from the RCA, LAD, and CIRC. Some lesions were complex with fibrous caps, hemorrhage, calcification, and foam cells (Figure 5).
Representative H&E stained sections from each group are shown: LDLR−/− (A,B), LDLR +/− (C,D), and LDLR +/+ (E,F). Complex lesions were seen in the LDLR−/− pigs (A,B) that exhibited hemorrhage, possible areas of calcification, fibrous caps and foam cells.
By morphometric methods, the coronary arteries from LDLR−/− pigs had overall significantly larger intimal area, percent stenosis, and intimal area as percent medial area than the LDLR+/+ or LDLR+/− coronary arteries. This difference was predominantly in the distal portion of the arteries with significantly larger percent stenosis and intimal area as percent medial area in the distal portion of coronary arteries from the LDLR−/− pigs (Table 5).
We have produced new models of hypercholesterolemia and coronary and aortic atherosclerosis in the commonly studied Yucatan miniature pig breed by disrupting the endogenous LDLR gene. LDLR+/− pigs exhibit mild, yet consistent elevated cholesterol that is present at birth and persists when fed a zero-cholesterol, low fat diet. LDLR−/− animals are born with severe hypercholesterolemia and develop atherosclerotic lesions by 7 months of age. The phenotypes of the LDLR+/− and LDLR−/− pigs are accelerated when fed a high fat, high cholesterol diet.
Our results are consistent with human FH, a dominant disorder exhibiting a gene dosage effect in which LDLR homozygotes exhibit a more severe phenotype than LDLR heterozygotes. Previous studies in Rapacz spontaneous hypercholesterolemic pigs (LDLR-R84C homozygotes) suggested that FH is a recessive disease in pigs, because cholesterol levels in heterozygotes did not differ from wild-type controls. However, this is likely due to the high genetic variability seen in these animals, including the presence of various ApoB alleles and other genetic modifiers . The more homogenous genetic background of the LDLR-targeted Yucatan miniature pigs allows the difference between LDLR+/+ and LDLR+/− animals to be more readily observed.
LDLR-targeted Yucatan miniature pigs offer several advantages over existing large animal models of hypercholesterolemia and atherosclerosis. First, at 60–75 kg, mature Yucatan miniature pigs are one-third to one-half the size of domestic pigs (including the Rapacz FH pigs) making them more representative of average human size and easier for most researchers to conduct studies. This is important for studies directed at the development of new human devices and diagnostic equipment. Second, due to the “knock-out” nature of the gene disruption, a more severe, and thus more rapidly developing, atherosclerosis is possible in the homozygotes compared to the Rapacz or PCSK9-D374Y transgenic pigs. This will decrease the duration and costs of studies. Furthermore, since the heterozygote pigs have only one functional LDLR allele, they are susceptible to accelerated, diet-induced hypercholesterolemia and atherosclerosis (compared to wild-type animals). This makes them uniquely suited for the development of therapeutic approaches that directly, or indirectly, induce LDL receptor expression and the evaluation of a treatment's ability to impede or even reverse the progression of atherosclerosis. This may not be possible with the constitutive transgene expression in the PCSK9-D374Y pig. Finally, because of the homogeneous genetic background of the miniature pig line, the variability in phenotype and response to interventions seen in current models should also be reduced.
This model also has some limitations, with perhaps the greatest being its size and the challenges that come with it. A large animal model requires specialized housing, trained staff, unique study facilities, and in some cases, specially formulated diets. Most current animal models of hypercholesterolemia and atherosclerosis require a highly modified diet often consisting of 1–4% pure cholesterol and sodium cholate, which are not typical of human diets and with the latter being possibly toxic and counterproductive . Furthermore, these diets are cost-prohibitive for many researchers, with daily feed costs being ~40 times more expensive than normal swine diets. We used a diet that is more representative of human consumption containing natural sources of saturated fat and cholesterol, which is significantly cheaper (2-3X normal swine diets). A pig's size is not ideal for early-stage drug development, due to the amount of test compound required. Accordingly, pigs may be better suited to bridge the large gap that exists between small animal models and human clinical trials. For example, several recent studies have shown promising results in the current small animal models of atherosclerosis, only to fail in phase 3 studies . If the porcine model were to offer more predictive efficacy, the benefits would far outweigh the costs. Another limitation is that pigs, like mice, lack cholesteryl ester transfer protein (CETP). Inhibition of human CETP to increase circulating HDL has been an area of intense study recently, however to date, no drugs in this class have progressed beyond clinical trials .
Several issues regarding the LDLR-targeted Yucatan miniature pigs remain to be addressed. We describe the presence of advanced atherosclerotic lesions in eleven-month-old LDLR−/− pigs fed a high fat, high cholesterol diet, but we did not observe plaque rupture or thrombosis. A longer study is underway to better establish the full spectrum and timeline of phenotypic development, though the results presented here are encouraging. The present study also does not address the impact of gender and puberty on phenotype. Our standard diet study only looked at pigs up to 6–7 months, which is the point at which pigs undergo puberty. We saw no discernable differences between males and females up to that point. The high fat, high cholesterol diet study only looked at castrated males and females, and again, no differences in atherosclerosis severity were seen. Finally, it is obvious that an animal model with improved predictive efficacy is needed. While that will take more time to demonstrate, we are currently seeking to validate that drugs that have been successful in humans are equally effective in the porcine model. Perhaps more importantly, we would also like to know whether LDLR-targeted pigs would have predicted the failure in humans of drugs that were initially shown to be efficacious in mice.
The LDLR-targeted Yucatan miniature pigs provide a versatile new model system for pursuing research into new devices, diagnostic tools, and therapeutics for human cardiovascular disease. This study further validates genetically engineered pigs as useful biomedical models of human disease.
Genotyping results from LDLR-targeted pig fetal fibroblasts. A. Example of PCR results. Primers amplified a 1.5 kb product from the wild-type allele and 3.2 kb product from the LDLR-targeted allele. Lanes 1–5 are examples of PCR-positive cell clones. Lane 6 is a wild-type cell clone. B. Southern blot of whole genome amplified DNA. (Left) XmnI digested genomic DNA was hybridized with a probe that detects porcine LDLR downstream of the targeting vector boundary. The LDLR-targeted allele produced an approximately 7.8 kb band, and the wild-type band is approximately 6.0 kb. (Right) The same DNA was hybridized with a probe that detects the NeoR cassette, yielding only the targeted 7.8 kb band. Lane 3 is an example of a properly targeted cell line. Lane 5 is a wild-type control.
List of PCR and Sequencing Primers.
We thank Todd Honkomp, Trisha Smit, Tommy Zerse, Brian Huedepohl, and Jenn Walz for technical assistance. We thank Martha Wilson and Matt Davis (Wake Forest University) for assistance with lipid analysis. We thank Michael Spurlock for assistance with formulating diets. We also thank John Swart for helpful discussions and comments on the manuscript.
Conceived and designed the experiments: FAR TCN CSR. Performed the experiments: BTD XJW JAR JTS EPM DAB FAR TCN CSR. Analyzed the data: BTD XJW EPM DAB TCN CSR. Contributed reagents/materials/analysis tools: DAB. Wrote the paper: BTD XJW EPM TCN CSR.
- 1. Rogers CS, Hao Y, Rokhlina T, Samuel M, Stoltz DA, et al. (2008) Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer. J Clin Invest 118: 1571–1577. doi: 10.1172/jci34773
- 2. Rogers CS, Stoltz DA, Meyerholz DK, Ostedgaard LS, Rokhlina T, et al. (2008) Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs. Science 321: 1837–1841. doi: 10.1126/science.1163600
- 3. Stoltz DA, Meyerholz DK, Pezzulo AA, Ramachandran S, Rogan MP, et al. (2010) Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth. Sci Transl Med 2: 29ra31. doi: 10.1126/scitranslmed.3000928
- 4. Ostedgaard LS, Meyerholz DK, Chen JH, Pezzulo AA, Karp PH, et al. (2011) The DeltaF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs. Sci Transl Med 3: 74ra24. doi: 10.1126/scitranslmed.3001868
- 5. Rogan MP, Reznikov LR, Pezzulo AA, Gansemer ND, Samuel M, et al. (2010) Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth. Proc Natl Acad Sci U S A 107: 20571–20575. doi: 10.1073/pnas.1015281107
- 6. Pezzulo AA, Tang XX, Hoegger MJ, Alaiwa MH, Ramachandran S, et al. (2012) Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung. Nature 487: 109–113. doi: 10.1038/nature11130
- 7. Johnson GJ, Griggs TR, Badimon L (1999) The utility of animal models in the preclinical study of interventions to prevent human coronary artery restenosis: analysis and recommendations. On behalf of the Subcommittee on Animal, Cellular and Molecular Models of Thrombosis and Haemostasis of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 81: 835–843.
- 8. Lusis AJ, Mar R, Pajukanta P (2004) Genetics of atherosclerosis. Annu Rev Genomics Hum Genet 5: 189–218. doi: 10.1146/annurev.genom.5.061903.175930
- 9. Sanz J, Moreno PR, Fuster V (2013) The year in atherothrombosis. J Am Coll Cardiol 62: 1131–1143. doi: 10.1016/j.jacc.2013.06.045
- 10. Libby P, Lichtman AH, Hansson GK (2013) Immune effector mechanisms implicated in atherosclerosis: from mice to humans. Immunity 38: 1092–1104. doi: 10.1016/j.immuni.2013.06.009
- 11. Tabas I, Williams KJ, Boren J (2007) Subendothelial lipoprotein retention as the initiating process in atherosclerosis: update and therapeutic implications. Circulation 116: 1832–1844. doi: 10.1161/circulationaha.106.676890
- 12. Little WC, Constantinescu M, Applegate RJ, Kutcher MA, Burrows MT, et al. (1988) Can coronary angiography predict the site of a subsequent myocardial infarction in patients with mild-to-moderate coronary artery disease? Circulation 78: 1157–1166. doi: 10.1161/01.cir.78.5.1157
- 13. Stone GW, Maehara A, Lansky AJ, de Bruyne B, Cristea E, et al. (2011) A prospective natural-history study of coronary atherosclerosis. N Engl J Med 364: 226–235. doi: 10.1056/nejmoa1002358
- 14. Nichols TC (2013) Bad cholesterol breaking really bad. Blood 122: 3551–3553. doi: 10.1182/blood-2013-09-527697
- 15. Rader DJ, Cohen J, Hobbs HH (2003) Monogenic hypercholesterolemia: new insights in pathogenesis and treatment. J Clin Invest 111: 1795–1803. doi: 10.1172/jci18925
- 16. Daugherty A (2002) Mouse models of atherosclerosis. Am J Med Sci 323: 3–10. doi: 10.1097/00000441-200201000-00002
- 17. Ishibashi S, Brown MS, Goldstein JL, Gerard RD, Hammer RE, et al. (1993) Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery. J Clin Invest 92: 883–893. doi: 10.1172/jci116663
- 18. Plump AS, Smith JD, Hayek T, Aalto-Setala K, Walsh A, et al. (1992) Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells. Cell 71: 343–353. doi: 10.1016/0092-8674(92)90362-g
- 19. Purcell-Huynh DA, Farese RV Jr, Johnson DF, Flynn LM, Pierotti V, et al. (1995) Transgenic mice expressing high levels of human apolipoprotein B develop severe atherosclerotic lesions in response to a high-fat diet. J Clin Invest 95: 2246–2257. doi: 10.1172/jci117915
- 20. Bentzon JF, Falk E (2010) Atherosclerotic lesions in mouse and man: is it the same disease? Curr Opin Lipidol 21: 434–440. doi: 10.1097/mol.0b013e32833ded6a
- 21. Benvenuti LA, Onishi RY, Gutierrez PS, de Lourdes Higuchi M (2005) Different patterns of atherosclerotic remodeling in the thoracic and abdominal aorta. Clinics (Sao Paulo) 60: 355–360.
- 22. Kobayashi T, Ito T, Shiomi M (2011) Roles of the WHHL rabbit in translational research on hypercholesterolemia and cardiovascular diseases. J Biomed Biotechnol 2011: 406473. doi: 10.1155/2011/406473
- 23. Gerrity RG, Natarajan R, Nadler JL, Kimsey T (2001) Diabetes-induced accelerated atherosclerosis in swine. Diabetes 50: 1654–1665. doi: 10.2337/diabetes.50.7.1654
- 24. Schwartz RS, Edelman E, Virmani R, Carter A, Granada JF, et al. (2008) Drug-eluting stents in preclinical studies: updated consensus recommendations for preclinical evaluation. Circ Cardiovasc Interv 1: 143–153. doi: 10.1161/circinterventions.108.789974
- 25. Onuma Y, Serruys PW, Perkins LE, Okamura T, Gonzalo N, et al. (2010) Intracoronary optical coherence tomography and histology at 1 month and 2, 3, and 4 years after implantation of everolimus-eluting bioresorbable vascular scaffolds in a porcine coronary artery model: an attempt to decipher the human optical coherence tomography images in the ABSORB trial. Circulation 122: 2288–2300. doi: 10.1161/circulationaha.109.921528
- 26. Gerrity RG, Goss JA, Soby L (1985) Control of monocyte recruitment by chemotactic factor(s) in lesion-prone areas of swine aorta. Arteriosclerosis 5: 55–66. doi: 10.1161/01.atv.5.1.55
- 27. Thomas WA, Lee KT, Kim DN (1985) Cell population kinetics in atherogenesis. Cell births and losses in intimal cell mass-derived lesions in the abdominal aorta of swine. Ann N Y Acad Sci 454: 305–315. doi: 10.1111/j.1749-6632.1985.tb11870.x
- 28. Mohiaddin RH, Burman ED, Prasad SK, Varghese A, Tan RS, et al. (2004) Glagov remodeling of the atherosclerotic aorta demonstrated by cardiovascular magnetic resonance: the CORDA asymptomatic subject plaque assessment research (CASPAR) project. J Cardiovasc Magn Reson 6: 517–525. doi: 10.1081/jcmr-120030576
- 29. Dixon JL, Stoops JD, Parker JL, Laughlin MH, Weisman GA, et al. (1999) Dyslipidemia and vascular dysfunction in diabetic pigs fed an atherogenic diet. Arterioscler Thromb Vasc Biol 19: 2981–2992. doi: 10.1161/01.atv.19.12.2981
- 30. Hasler-Rapacz J, Ellegren H, Fridolfsson AK, Kirkpatrick B, Kirk S, et al. (1998) Identification of a mutation in the low density lipoprotein receptor gene associated with recessive familial hypercholesterolemia in swine. Am J Med Genet 76: 379–386. doi: 10.1002/(sici)1096-8628(19980413)76:5<379::aid-ajmg3>3.0.co;2-i
- 31. Rapacz J, Hasler-Rapacz J, Taylor KM, Checovich WJ, Attie AD (1986) Lipoprotein mutations in pigs are associated with elevated plasma cholesterol and atherosclerosis. Science 234: 1573–1577. doi: 10.1126/science.3787263
- 32. Grunwald KA, Schueler K, Uelmen PJ, Lipton BA, Kaiser M, et al. (1999) Identification of a novel Arg—>Cys mutation in the LDL receptor that contributes to spontaneous hypercholesterolemia in pigs. J Lipid Res 40: 475–485.
- 33. Prescott MF, McBride CH, Hasler-Rapacz J, Von Linden J, Rapacz J (1991) Development of complex atherosclerotic lesions in pigs with inherited hyper-LDL cholesterolemia bearing mutant alleles for apolipoprotein B. Am J Pathol 139: 139–147.
- 34. Thim T, Hagensen MK, Drouet L, Bal Dit Sollier C, Bonneau M, et al. (2010) Familial hypercholesterolaemic downsized pig with human-like coronary atherosclerosis: a model for preclinical studies. EuroIntervention 6: 261–268. doi: 10.4244/eijv6i2a42
- 35. Al-Mashhadi RH, Sorensen CB, Kragh PM, Christoffersen C, Mortensen MB, et al. (2013) Familial hypercholesterolemia and atherosclerosis in cloned minipigs created by DNA transposition of a human PCSK9 gain-of-function mutant. Sci Transl Med 5: 166ra161. doi: 10.1126/scitranslmed.3004853
- 36. Lai L, Prather RS (2003) Production of cloned pigs by using somatic cells as donors. Cloning Stem Cells 5: 233–241. doi: 10.1089/153623003772032754
- 37. Pomp D, Good BA, Geisert RD, Corbin CJ, Conley AJ (1995) Sex identification in mammals with polymerase chain reaction and its use to examine sex effects on diameter of day-10 or -11 pig embryos. J Anim Sci 73: 1408–1415.
- 38. Walker SC, Shin T, Zaunbrecher GM, Romano JE, Johnson GA, et al. (2002) A highly efficient method for porcine cloning by nuclear transfer using in vitro-matured oocytes. Cloning Stem Cells 4: 105–112. doi: 10.1089/153623002320253283
- 39. Hobbs HH, Russell DW, Brown MS, Goldstein JL (1990) The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein. Annu Rev Genet 24: 133–170. doi: 10.1146/annurev.ge.24.120190.001025
- 40. Hickey RD, Lillegard JB, Fisher JE, McKenzie TJ, Hofherr SE, et al. (2011) Efficient production of Fah-null heterozygote pigs by chimeric adeno-associated virus-mediated gene knockout and somatic cell nuclear transfer. Hepatology 54: 1351–1359. doi: 10.1002/hep.24490
- 41. Wen J, Brogna S (2008) Nonsense-mediated mRNA decay. Biochem Soc Trans 36: 514–516. doi: 10.1042/bst0360514
- 42. Wang J, Chang YF, Hamilton JI, Wilkinson MF (2002) Nonsense-associated altered splicing: a frame-dependent response distinct from nonsense-mediated decay. Mol Cell 10: 951–957. doi: 10.1016/s1097-2765(02)00635-4
- 43. Lichtman AH, Clinton SK, Iiyama K, Connelly PW, Libby P, et al. (1999) Hyperlipidemia and atherosclerotic lesion development in LDL receptor-deficient mice fed defined semipurified diets with and without cholate. Arterioscler Thromb Vasc Biol 19: 1938–1944. doi: 10.1161/01.atv.19.8.1938
- 44. Agarwala A, Billheimer J, Rader DJ (2013) Mighty minipig in fight against cardiovascular disease. Sci Transl Med 5: 166fs161. doi: 10.1126/scitranslmed.3005369
- 45. Mohammadpour AH, Akhlaghi F (2013) Future of cholesteryl ester transfer protein (CETP) inhibitors: a pharmacological perspective. Clin Pharmacokinet 52: 615–626. doi: 10.1007/s40262-013-0071-8