http://orcid.org/0000-0003-4480-0862
Figures
Abstract
Increased transforming growth factor-β (TGF-β) signaling contributes to the pathophysiology of aortic aneurysm in Marfan syndrome (MFS). Recent reports indicate that a small but significant number of inflammatory cells are infiltrated into the aortic media and adventitia in MFS. However, little is known about the contribution of myeloid cells to aortic aneurysmal formation. In this study, we ablated the TGF-β type II receptor gene Tgfbr2 in myeloid cells of Fbn1C1039G/+ MFS mice (Fbn1C1039G/+;LysM-Cre/+;Tgfbr2fl/fl mice, hereinafter called Fbn1C1039G/+;Tgfbr2MyeKO) and evaluated macrophage infiltration and TGF-β signaling in the aorta. Aneurysmal formation with fragmentation and disarray of medial elastic fibers observed in MFS mice was significantly ameliorated in Fbn1C1039G/+;Tgfbr2MyeKO mice. In the aorta of Fbn1C1039G/+;Tgfbr2MyeKO mice, both canonical and noncanonical TGF-β signals were attenuated and the number of infiltrated F4/80-positive macrophages was significantly reduced. In vitro, TGF-β enhanced the migration capacity of RAW264.7 macrophages. These findings suggest that TGF-β signaling in myeloid cells promotes aortic aneurysmal formation and its inhibition might be a novel therapeutic target in MFS.
Citation: Hara H, Maemura S, Fujiwara T, Takeda N, Ishii S, Yagi H, et al. (2020) Inhibition of transforming growth factor-β signaling in myeloid cells ameliorates aortic aneurysmal formation in Marfan syndrome. PLoS ONE 15(11): e0239908. https://doi.org/10.1371/journal.pone.0239908
Editor: Tohru Minamino, Niigata Daigaku, JAPAN
Received: April 12, 2020; Accepted: September 15, 2020; Published: November 11, 2020
Copyright: © 2020 Hara 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.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This work was supported by JSPS KAKENHI Grant Number 19K08484 and Mochida Memorial Foundation for Medical and Pharmaceutical Research (NT). https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-19K08484/ http://www.mochida.co.jp/zaidan/ The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
MFS is a systemic disorder of connective tissues caused by pathogenic variants in the FBN1 gene, which encodes the major component of the extracellular matrix microfibril fibrillin-1 [1]. Fibrillin-1 binds to the latent complex of TGF-β and regulates its activity in response to pathophysiological stresses. FBN1 pathogenic variants that affect the structure or function of fibrillin-1 protein not only cause structural weakness of the connective tissue but also stimulate improper latent TGF-β activation [2, 3]. Among the diverse manifestations of MFS, aortic aneurysm and dissection are the most serious and the leading causes of death [4]. The aortic TGF-β signaling is activated in MFS, and treatment of adult MFS mice with a TGF-β neutralizing antibody (TGF-NAb) prevents aortic root dilatation associated with attenuation of the canonical Smad and the noncanonical extracellular signal-regulated kinase (ERK) signaling pathways [5]. On the contrary, early initiation of TGF-NAb treatment from postnatal day 16 (P16) in fibrillin-1 hypomorphic (Fbn1mgR/mgR) mice exacerbates aneurysmal formation, but the initiation from P45 ameliorates it [6]. Adult mice with a conditional tamoxifen-inducible biallelic disruption of Tgfbr2 in smooth muscle cells (Myh11-CreERT2;Tgfbr2fl/fl) develop aortic aneurysm [7]. These findings suggest that TGF-β signaling plays pivotal roles both in early postnatal aortic development and adult aortic homeostasis.
Recent studies show that a small but significant number of inflammatory cells are infiltrated into the aortic media and adventitia [8, 9]. Importantly, the number of inflammatory cells infiltrated into the aorta was larger in patients who required prophylactic repair of the aorta early in life, compared to patients who did not need prophylactic repair until elderly [8]. It is possible that inflammatory cells play a crucial role in aortic aneurysmal formation.
Here, we hypothesized that upregulated TGF-β activity in myeloid cells plays an important role in the disease progression. In the present study, we ablated the Tgfbr2 gene in myeloid cells of Fbn1C1039G/+ MFS mice and evaluated the effect on aortic aneurysmal formation in MFS.
Methods
Animals
Generation of homozygous Tgfbr2-floxed (Tgfbr2fl/fl) mice and genotyping have been previously described [10]. Fbn1C1039G/+ and LysM-Cre/+ mice were obtained from the Jackson Laboratory [11, 12]. All animal experiments were approved by the University of Tokyo Ethics Committee for Animal Experiments and strictly adhered to the guidelines of the University of Tokyo for animal experiments. Mice were monitored daily by animal facility staff and observed for signs of stress and distress.
Efficacy of Cre-mediated recombination in Tgfbr2MyeKO mice
To confirm the previously reported high-efficacy of Cre-mediated recombination in Tgfbr2MyeKO mice [13], macrophages were obtained from the peritoneal cavity of 6-week-old mice 4 days after injection of 4% thioglycollate (211260; Becton Dickinson and Company). Total RNA isolation, cDNA conversion, and semi-quantitative reverse transcription polymerase chain reaction (PCR) were performed as previously reported [14, 15]. The PCR primers used were as follows (forward and reverse, respectively): Tgfbr2, 5’-GCAAGTTTTGCGATGTGAGA-3’ and 5’-GGCATCTTCCAGAGTGAAGC-3’; 18S rRNA, 5’-CGGCTACCACATCCAAGGAA-3’, and 5’-AGCTGGAATTACCGCGGC-3’.
Noninvasive blood pressure measurement and ultrasonography
Systolic blood pressure was measured using a tail-cuff method (MK-2000ST; Muromachi Kikai). Ultrasonography was performed using the Vevo 2100 Imaging System (VisualSonics) while mice were anesthetized with 2.5% isoflurane. The luminal diameters of the aortic root were measured at the age of 8, 12, and 30 weeks by B-mode imaging.
Macroscopic images and histological analysis
Before excision of aorta, mice were euthanized by isoflurane overexposure. Following intra-cardiac perfusion of 4% paraformaldehyde, thoracic aorta was cleared of surrounding tissue and digitally captured using Leica MZ10 F microscope and Leica DFC450 C camera.
Tissue sections (5 μm) were prepared at the proximal ascending aorta (just above sinotubular junction). Elastica van Gieson staining was used to visualize the aortic elastic fiber structure. Elastic fiber breaks were defined as the presence of discernable breaks of continuous elastin fiber and counted circumferentially in all laminae [16, 17]. Rat anti-mouse monoclonal F4/80 antibody (MCA497; Bio-Rad) was used for immunohistochemical staining to recognize macrophages at the dilution of 1:200. The VECTASTAIN Elite ABC system (PK-6104; Vector Laboratories) was used for sensitive avidin/biotin-based peroxidase system and hematoxylin was used for counterstain of nuclei. The number of infiltrated macrophages was determined by counting cells at 40× magnification from four random fields, and the average number per area of aortic adventitia was used as an individual value [18, 19]. Rabbit-anti-mouse monoclonal phospho-Smad2/3 antibody (#3108; Cell Signaling Technology) was used as a primary antibody at the dilution of 1:100. The signal was visualized by ImmPRESS Reagent (MP-7401; Vector Laboratories) and TSA Fluorescein (SAT701B001EA; Perkin Elmer). DAPI (D523; Wako) was used for nuclei staining prior to mounting with VECTASHIELD (H-1000; Vector Laboratories). The ratio of positively stained nuclei to the total number of nuclei in the aorta was determined at 20× magnification from three random fields, and the average percentage was used as an individual value [20, 21]. Rabbit-anti-mouse polyclonal phospho-ERK1/2 antibody (#9101; Cell Signaling Technology) was used as a primary antibody at the dilution of 1:200. The signal was visualized by ImmPRESS Reagent (MP-7401; Vector Laboratories). 3, 3'-Diaminobenzidine tetrahydrochloride (SK-4100; Vector Laboratories) was used as substrate for horseradish peroxidase. The ratio of positively stained area to the total area of the aorta was determined at 40× magnification from three random fields, and the average percentage was used as an individual value [22]. Digital images of tissue sections were obtained using Olympus BX 51 microscope and Olympus DP 70 camera. Brightness and contrast were adjusted linearly across the entirety of each image.
MTS cell proliferation assay
RAW264.7 cells under fetal calf serum-free starved condition were incubated with the vehicle or 5 ng/mL of recombinant human TGF-β1 (209–16544; Wako) for 24 hours. Then, the cell proliferation rate was evaluated using a CellTiter 96® AQueous One Solution Cell Proliferation Assay kit (G3582; Promega) and a microplate-reading luminometer (Wallac Arvo Mx 1420; PerkinElmer) [23].
In vitro cell migration assay
RAW264.7 cells were grown to confluence before the cell monolayer was scratched using a sterile P200 micropipette tip [24]. Next, cells were washed with phosphate-buffered saline, cultured at 37°C in fetal calf serum-free DMEM and treated with the vehicle or 5 ng/mL of recombinant human TGF-β1 (Wako) for 24 hours. The images of the scratched area were captured immediately after the scratch and after 24 hours to monitor cell migration. The migration capacity was quantified from the area between the edges of cells in the scratch zone.
Statistical analysis
All analyses were performed using JMP Pro 14.2.0 (SAS Institute). Data are shown as mean ± standard deviation. The assumption of homogeneity of variance was tested using Levene’s test. The significance of differences among means was evaluated using Student’s t-test, Welch’s t-test, one-way analysis of variance followed by post hoc Tukey–Kramer test, or Kruskal–Wallis test followed by post hoc Steel–Dwass test. P-values < 0.05 were considered statistically significant.
Results
To examine the impact of TGF-β signaling in myeloid cells on aortic aneurysmal formation in MFS, we ablated Tgfbr2 in myeloid cells in Fbn1C1039G/+ heterozygous MFS mice by crossing with myeloid-specific Tgfbr2 knockout mice (Tgfbr2MyeKO mice). Exon 2 of Tgfbr2 (169 bp) was flanked with loxP sites and Cre-mediated recombination produced out-of-frame transcripts in myeloid cells of Tgfbr2MyeKO mice (S1 Fig) [10, 13]. Compared to control wild-type mice (Tgfbr2fl/fl) and MFS mice (Fbn1C1039G/+;Tgfbr2fl/fl), myeloid-specific Tgfbr2 disruption did not affect systolic blood pressure or body weight of Tgfbr2MyeKO and Fbn1C1039G/+;Tgfbr2MyeKO mice (S2 Fig).
Fbn1C1039G/+;Tgfbr2fl/fl MFS mice developed progressive aortic root dilatation to 30 weeks of age without early death. On the other hand, aneurysmal formation was significantly suppressed in both male and female Fbn1C1039G/+;Tgfbr2MyeKO mice, and Tgfbr2MyeKO mice did not develop any aortic phenotypes (Fig 1). Histological analysis revealed aberrant thickening of the aortic media with fragmentation and disarray of elastic fibers in Fbn1C1039G/+;Tgfbr2fl/fl mice, but they were markedly reduced in Fbn1C1039G/+;Tgfbr2MyeKO mice (Fig 2). These findings suggest that TGF-β signaling in myeloid cells is inessential in normal aortic development and homeostasis but it promotes the progression of aortic aneurysmal formation in MFS.
(A, B) Representative macroscopic appearance (A) and ultrasound images (B) of the thoracic aorta at 30 weeks of age in Tgfbr2 fl/fl, Tgfbr2MyeKO, Fbn1C1039G/+;Tgfbr2 fl/fl, and Fbn1 C1039G/+;Tgfbr2MyeKO mice. Scale bar, 1 mm. Arrows indicate aortic root (AoR); AAo, Ascending aorta. (C) Aortic root diameter measured by ultrasonography at 8, 12, and 30 weeks of age. n = 3–12 per group. Data are shown as mean ± standard deviation. *p < 0.05, **p < 0.01, ***p < 0.001.
(A) Representative images of Elastica van Gieson staining of the proximal ascending aorta at 30 weeks of age in Tgfbr2 fl/fl, Tgfbr2MyeKO, Fbn1C1039G/+;Tgfbr2 fl/fl, and Fbn1 C1039G/+;Tgfbr2MyeKO mice. Scale bar, 100 μm. (B) Average number of elastic fiber breaks per section. All mice were male. n = 4–7 per group. Data are shown as mean ± standard deviation. *p < 0.05, **p < 0.01, ***p < 0.001.
Next, we evaluated macrophage infiltration into the aneurysmal wall, as macrophage is reported to be a major component of infiltrating inflammatory cells [8]. F4/80-positive macrophages were significantly increased mainly in the adventitia of the proximal ascending aorta (just above sinotubular junction) of Fbn1C1039G/+;Tgfbr2fl/fl mice at 30 weeks of age. However, the number of macrophages infiltrated into the aorta of Fbn1C1039G/+;Tgfbr2MyeKO mice was significantly reduced compared to Fbn1C1039G/+;Tgfbr2fl/fl mice (Fig 3).
(A) Representative images of F4/80 (marker of macrophage, red arrowheads) of the proximal ascending aorta at 30 weeks of age in Tgfbr2 fl/fl, Tgfbr2MyeKO, Fbn1C1039G/+;Tgfbr2 fl/fl, and Fbn1 C1039G/+;Tgfbr2MyeKO mice. Cell nuclei were counterstained with hematoxylin. All mice were male. Scale bar, 50 μm (20 μm in inset). (B) Average number of F4/80-positive macrophages per area of aortic adventitia. Four random 40× magnification fields were investigated. All mice were male. n = 4–7 per group. Data are shown as mean ± standard deviation. *p < 0.05, ***p < 0.001.
We further examined the effect of myeloid-specific Tgfbr2 disruption on TGF-β signaling-related pathways in the aortic wall. Increased Smad2/3 and ERK1/2 phosphorylations were evident in the ascending aorta of Fbn1C1039G/+;Tgfbr2fl/fl mice, but they were remarkably attenuated in Fbn1C1039G/+;Tgfbr2MyeKO mice (Fig 4).
(A, B) Representative phospho-Smad2/3 (A) and phospho-ERK1/2 (B) staining of the proximal ascending aorta at 30 weeks of age in Tgfbr2 fl/fl, Tgfbr2MyeKO, Fbn1C1039G/+;Tgfbr2 fl/fl, and Fbn1 C1039G/+;Tgfbr2MyeKO mice. Scale bar, 50 μm. Arrowheads show the representative positive staining. (C) Average percentage of positive staining of phospho-Smad2/3 per nuclei. Three random 20× magnification fields were investigated. All mice were male. n = 4–7 per group. Data are shown as mean ± standard deviation. *p < 0.05, **p < 0.01. (D) Average percentage of positive stained area of phospho-ERK1/2 per aortic area. Three random 40× magnification fields were investigated. All mice were male. n = 4–7 per group. Data are shown as mean ± standard deviation. *p < 0.05, **p < 0.01, ***p < 0.001.
Finally, we investigated the effect of TGF-β on the migration capacity of macrophage using an in vitro monolayer wound healing assay. After RAW264.7 cells, a murine macrophage cell line, reached confluence, an artificial gap was created in the macrophage monolayer using a straight line. TGF-β treatment (5 ng/mL) did not promote cell proliferation (Fig 5A) but significantly enhanced the wound closure rate 24 hours after scratching (Fig 5B and 5C). These data indicates that TGF-β could upregulate the migration capacity of RAW264.7 macrophages.
(A) MTS cell proliferation assay. n = 6 per group. Data are shown as mean ± standard deviation. n.s, not significant. (B, C) In vitro cell migration assay. A monolayer of RAW264.7 cells was scratched with a P200 pipette tip, which induced migration of cells into the denuded area to close the wound in the presence or absence of TGF-β (5 ng/mL) for 24 hours. (B) Representative images obtained immediately after the scratch and after 24 hours. (C) The migration capacity was quantified from the area between the edges of cells in the scratch zone. n = 10 per group. Data are shown as mean ± standard deviation. ***p < 0.001.
Discussion
In this study, we examined whether TGF-β signaling in myeloid cells plays a crucial role in aortic aneurysmal formation. Myeloid-specific Tgfbr2 gene ablation in MFS mice attenuated activation of TGF-β signaling and macrophage infiltration in the aorta. In Fbn1 C1039G/+;Tgfbr2MyeKO mice, aortic dilatation was already evident at 8 and 12 weeks of age, but it became less prominent as they grew up (Fig 1C). Therefore, myeloid-specific deletion of Tgfbr2 in MFS model mice ameliorated aortic aneurysmal formation, but it did not prevent the initiation of aortic aneurysmal formation. In addition, TGF-β enhanced the migration capacity of RAW264.7 macrophages in vitro. These findings suggest that TGF-β signaling in myeloid cells might promote the progression of aortic aneurysmal formation, and its inhibition might be a novel therapeutic target in MFS.
Tgfbr2MyeKO mice, lacking myeloid-specific TGF-β receptor II, but with normal hematopoiesis, have been used to investigate disease-specific roles of TGF-β signaling in myeloid cells [25–28]. In the present study, Tgfbr2 disruption in myeloid cells attenuated phosphorylations of Smad2/3 and ERK1/2 in the ascending aorta of MFS mice (Fig 4). In MFS, mutated FBN1 gene causes reduced or abnormal fibrillin-1 protein, which normally regulates TGF-β bioavailability by releasing latent TGF-β from the extracellular matrix in response to pathophysiological stimuli. Thus, the ensuing upregulation of TGF-β signaling cascades play crucial roles in MFS [3]. Angiotensin II type I blocker losartan has been reported to remarkably ameliorate activation of Smad2 and aortic aneurysmal formation in Fbn1C1039G/+ mice [29], but the mechanism is still not fully understood. It has also been demonstrated that the activation of ERK1/2 as the noncanonical pathway of TGF-β signaling serves as a prominent driver of aortic aneurysmal formation and ERK1/2 signal is inhibited by systemic TGF-β-neutralizing antibody treatment in Fbn1C1039G/+ mice [5]. Furthermore, selective inhibition of ERK1/2 activation ameliorated aortic growth in Fbn1C1039G/+ mice, whereas Smad2 signal was unchanged [5]. These data suggest that TGF-β-driven ERK1/2 activation strongly contributes to aneurysmal formation in MFS, and thus further investigation is needed to elucidate the role of TGF-β signaling in myeloid cells in the ERK1/2 phosphorylation in the aortic wall.
It has been reported that pre-treatment of TGF-β exerts biphasic effect on the migration capacity of RAW264.7 cells [30]. However, in the present study, continuous stimulation of TGF-β for 24 hours enhanced the migration capacity of RAW264.7 macrophages (Fig 5). We also demonstrated that Tgfbr2 disruption in myeloid cells reduced macrophage infiltration into the aortic wall (Fig 3). One possible reason for amelioration of aortic aneurysmal formation by myeloid-specific disruption of Tgfbr2 in MFS is the inhibitory effect on macrophage migration and invasion into the diseased aortic wall. Myeloid-specific deletion of Tgfbr2 is reported to reduce migration and invasion capacity of macrophages in tumor-bearing mice as well [26]. Myeloid-specific deletion of Tgfbr2 might alter the expression of adhesion molecules and cytokines and modulate migration capacity. Co-culture of FBN1-knocked-down vascular smooth muscle cells and macrophages derived from Tgfbr2MyeKO mice could partially recapitulate the in vivo context of MFS.
It has been shown that IL-6 recruits CCR2-positive monocytes which serve to amplify the inflammatory cascade, and IL-6 signaling contributes to Angiotensin II-induced aortic aneurysm [31]. Activation of IL-6 signaling has been demonstrated in hypomorphic Fbn1mgR/mgR mice [32]. Additionally, in the aorta of MFS and familial thoracic aortic aneurysm and dissection, the expression of adhesion molecules surrounding the vasa vasorum in the adventitia is increased [8]. Taken together, reduction of macrophage invasion into the diseased aortic wall might suppress IL-6 signaling and adhesion molecules in the aneurysmal wall of Fbn1C1039G/+;Tgfbr2MyeKO mice. This hypothesis should be confirmed in the near future.
TGF-β signaling has been shown to play an important role in phenotypic differentiation of macrophage in various pathological situations [33, 34]. Hematopoietic-specific Tgfbr2 deletion has been reported to suppress the expression of Galectin-3, which regulates M2 macrophage polarization, in bone marrow-derived macrophage/monocytes [33]. TGF-β inhibits M1 polarization and promotes M2 polarization in human THP-1 macrophage [34]. Although, to the best of our knowledge, the polarization of macrophage in MFS has not been evaluated, we speculate that phenotypic alteration of macrophage as well as change in the migration capacity due to increased TGF-β signaling may contribute to the progression of aortic aneurysm in MFS. Further investigation of M1/M2 phenotypic alteration and migration capacity of bone marrow-derived macrophage/monocytes from Fbn1C1039G/+;Tgfbr2MyeKO mice is needed to elucidate the mechanism.
This study demonstrated for the first time that TGF-β signaling disruption in myeloid cells ameliorated Fbn1C1039G/+ MFS aortopathy, where F4/80-positive macrophage infiltration and both canonical and noncanonical TGF-β signals were markedly reduced. Our findings suggest that inhibition of TGF-β signaling in myeloid cells might be a novel therapeutic target in MFS.
Supporting information
S1 Checklist. The ARRIVE guidelines checklist.
https://doi.org/10.1371/journal.pone.0239908.s001
(PDF)
S1 Fig. Efficacy of Cre-mediated loxP recombination in myeloid cells.
Semi-quantitative PCR of cDNA prepared from peritoneal macrophages was performed. PCR products for Tgfbr2 and 18s are 197 bp and 188 bp.
https://doi.org/10.1371/journal.pone.0239908.s002
(TIF)
S2 Fig. Effects of Tgfbr2 deletion in myeloid cells on blood pressure and body weight.
Systolic blood pressure (A) and body weight (B) at 30 weeks of age in Tgfbr2 fl/f, Tgfbr2MyeKO, Fbn1C1039G/+;Tgfbr2 fl/fl, and Fbn1 C1039G/+;Tgfbr2MyeKO mice. n = 4–12 per group. Data are shown as mean ± standard deviation. n.s, not significant.
https://doi.org/10.1371/journal.pone.0239908.s003
(TIF)
S1 Raw image. Original image of gel (for S1 Fig).
Products amplified by semi-quantitative reverse transcription polymerase chain reaction using Tgfbr2 and 18s primers were separated by 1.2% agarose gel electrophoresis.
https://doi.org/10.1371/journal.pone.0239908.s004
(PDF)
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