Identification of a host collagen inducing factor from the excretory secretory proteins of Trichinella spiralis

Background In a previous study, we found that Trichinella spiralis muscle larva excretory and secretory proteins (ES-P) most likely activate collagen synthesis via TGF-β/Smad signaling, and this event could influence collagen capsule formation. Methodology/Principal findings In order to identify the specific collagen inducing factor, ES-P was fractionated by a Superdex 200 10/300 GL column. We obtained three large fractions, F1, F2, and F3, but only F3 had collagen gene inducing ability. After immunoscreening, 10 collagen inducing factor candidates were identified. Among them, TS 15–1 and TS 15–2 were identical to the putative trypsin of T. spiralis. The deduced TS 15–1 (M.W. = 72 kDa) had two conserved catalytic motifs, an N-terminal Tryp_SPc domain (TS 15-1n) and a C-terminal Tryp_SPc domain (TS 15-1c). To determine their collagen inducing ability, recombinant proteins (rTS 15-1n and rTS 15-1c) were produced using the pET-28a expression system. TS 15–1 is highly expressed during the muscle larval stage and has strong antigenicity. We determined that rTS 15-1c could elevate collagen I via activation of the TGF-β1 signaling pathway in vitro and in vivo. Conclusion/Significance In conclusion, we identified a host collagen inducing factor from T. spiralis ES-P using immunoscreening and demonstrated its molecular characteristics and functions.


Introduction
Trichinella spiralis can make collagen capsules in host muscles during their life cycle that surround muscle stage larvae and might protect the larvae from the host immune system. This phenomenon can be understood as the parasite creating a simple structure to protect itself, but when examined closely, numerous different mechanisms are involved in this stage of the parasite's life. Division of the host muscle cell nucleus, regulation of host cell cycling, huge elevation of host collagen gene expression, and generation of new blood vessels around the collagen capsule are observed during nurse cell formation by T. spiralis [1][2][3][4]. The process of nurse cell formation induces de-differentiation, cell cycle re-entry, arrest of infected muscle cells, and activation, proliferation, and differentiation of satellite cells. These events are very similar to those occurring during muscle cell regeneration and repair [2].
In a previous study, we found that T. spiralis excretory and secretory proteins (ES-P) most likely activate collagen synthesis via TGF-β/Smad signaling, and this event could influence collagen capsule formation [5]. These events were closely related with protease activated receptor 2 (PAR2), which was activated by various serine proteases [5]. However, the question of which protease in T. spiralis ES-P has a role in collagen gene expression of host muscle cells is still unanswered. The identification of a specific collagen gene inducer from T. spiralis could be exploited as a therapeutic and/or cosmetic agent. In this study, we isolated and characterized the collagen gene expression inducer from T. spiralis ES-P by immunoscreening and investigated the candidate for its usefulness as a wound healing therapeutic agent.

Isolation of muscle larvae and extraction of whole parasite proteins
The T. spiralis strain (isolate code ISS623) used in this study has been maintained in our laboratory via serial passage in rats. For acquisition of muscle larva, eviscerated mouse carcasses were cut into pieces, followed by digestion in 1% pepsin 1% hydrochloride digestion fluid (artificial gastric juice) for 1 hr at 37˚C with stirring. Larvae were collected manually from muscle digested solution under microscopy and washed 6 times with sterile PBS containing 100 μg/ml ampicillin, 5 μg/ml kanamycin and 50 μg/ml tetracyclin. After collection, in order to prevent contamination with the host material, worms were thoroughly and carefully washed several 3 times with PBS. Whole parasite proteins (total extract; TE) was obtained from muscle larva according to previous study [6]. In brief, muscle larva were rinsed in PBS and homogenized in 50 mM Tris-HCl (pH 7.5) with a glass homogenizer. The homogenates were briefly sonicated and then centrifuged for 30 min at 12,000 × g and 4˚C. The supernatant (TE) was stored at -20˚C.

Isolation of adult worm and new born larvae (NBL)
Small intestines were removed on the day 6 after infection from infected rat, opened, sliced by 2 cm, washed with PBS, and incubated for 1 hr at 37˚C in PBS containing antibiotics. Adult worms were collected on a PBS, washed 3 times with PBS containing antibiotics, and incubated for 24 hrs in serum-free RPMI 1640 medium containing antibiotics. After incubation, NBL were passed through 40 μl nylon mesh (BC falcon, USA) to be separated from adult worms.

Extraction of ES-P from muscle larvae and fractionation of ES-P
Muscle larvae were isolated from T. spiralis infected mice (4 weeks after infection) and ES-P from cultured muscle larvae was obtained according to the previously reported method [5]. The ES-P was fractionated using gel filtration chromatography. ES-P (5 mg) in 10 ml PBS was applied to a Superdex 200 10/300 GL column (GE Healthcare, Uppsala, Sweden). The flow rate was 0.25 ml/min. Each 0.5 ml fraction was collected and protein quantity was measured by UV detection at 260 nm. Three big fractions, F1, F2, and F3, were acquired and used for collagen gene inducing experiments ( Fig 3A).

Mouse experiments
Twenty female C57BL/6 mice at the age of 6 weeks and twenty female 14 week-old mice were purchased from Samtako Co. (Gyeonggi-do, Korea). The skin of the left ear of each mouse was treated with T. spiralis ES-P (30 μg) or rTS 15-1c (30 μg) in PBS (total volume 50 μl) every day for 14 days, and that of the right ear was treated with PBS (Figs 1A and 7A). The mice were housed in a specific pathogen-free facility at the Institute for Laboratory Animals of Pusan National University.

Cell culture and in vitro stimulation
In order to compare the expression level of type I collagen and their signal pathway related genes, mouse fibroblast (MEF) cells were used in this study because type I collagen was preferentially synthesized by two cell types, the osteoblast and the fibroblast [7]. MEF cells were isolated from C57BL/6 mouse fetuses 10 days after fertilization [8]. MEF cells were incubated in DMEM (Difco) with 5% FBS and 5 × 10 5 cells were plated in 24-well plates and incubated overnight at 37˚C in 5% CO 2 . The cells were treated with ES-P, boiled-ES-P, F1, F2, F3, boiled F3, TS 15-1c, and TS 15-1n (final conc. 1 μg/ml); ES-P with PMSF (serine protease inhibitor, final conc. 1 mM; Sigma-Aldrich, USA), F3 with PMSF for 2 hrs.

Zymography
Gelatin-gel containing 0.2% gelatin was prepared from gelatin-stock solution. The proteins, T. spiralis ES proteins, TS 15-1c, and TS 15-1n were mixed with 2 × sample buffer (1 M Tris pH 6.8, 1% bromphenol blue, glycerol, β-mercaptoethanol), and the gel loaded with these proteins was run with 1 × Tris-Glycine SDS running buffer on 125 V for 2 hrs at 4˚C. After running, the gel was washed to remove the SDS and re-natured proteinase activity with zymogram renaturing buffer (2.5% Triton X-100). The gel was developed with zymogram developing buffer (0.5 M Tris-HCl pH 7.6, 0.02 M NaCl, 0.5 mM CaCl 2 ) for 30 min at room temperature. The gel was incubated with developing buffer at 37˚C for 8 hrs. The gel was stained with Coomassie Blue R-250 for 30 min and distained with an appropriate destaining solution (Bio-Rad laboratories, Inc., USA).

Real-time PCR
Homogenized ear tissues were mixed with TRIzol (Invitrogen, Germany), and RNA extraction and cDNA synthesis (Invitrogen, Germany) was performed in accordance with the manufacturer's protocols. Expression levels of several genes were determined with real-time RT-PCR using the iCycler (Bio-Rad laboratories Inc., USA) real-time PCR machine. Primer sequences for collagen I, TGF-β, smad2, smad3, and GAPDH, and PCR conditions were identical to those mentioned in the previous study [5]. To evaluate variation of Ts-15-1 gene expression during T. spiralis life cycle, total RNAs were extracted from new born larva, adult worm, muscle larva and T. spiralis infected mouse muscle (1, 2, and 4 weeks after infection) using TRIzol (Invitrogen, Germany), and cDNA synthesis (Invitrogen, Germany) was performed in accordance with the manufacturer's protocols. Expression levels of several genes were determined with real-time RT-PCR using the iCycler (Bio-Rad laboratories Inc., USA) real-time PCR machine. The primer sequences for the putative trypsin (TS 15-1c), and T. spiralis GAPDH were 5 0 -TTG GAA TGA CGC TGA TTG -3 0 , 5 0 -GTG GCT TAT GAT GGT AGG AGA AT -3 0 and 5 0 -CAG GTG CTG ATT ACG CTG TT -3 0 , R-5 0 -ACG CCA ATG CTT ACC AGA T -3 0 respectively. Amplification of two genes was performed under the following conditions: 1 min 30 sec host start at 95˚C, followed by denaturation at 95˚C for 25 sec, primer annealing at 50~55˚C for 20 sec, and elongation at 72˚C and 30 sec for 40 cycles. Fluorescent DNA-binding dye SYBR was monitored after each cycle at 50~55˚C. An iCycler multi-color real-time PCR detection system (Bio-Rad Laboratories) was used for estimation of expression levels. Then, using the Gene-x program (Bio-Rad Laboratories), relative expression of the gene was calculated as the ratio to a T. spiralis GAPDH gene.

Immunoscreening of cDNA library
A cDNA library generated from 60,000 plaques forming units of T. spiralis muscle larvae was screened with the α-TS F3 antibody. Immunoscreening was performed using the SMART cDNA Library Construction Kit (Clontech, USA) in accordance with the manufacturer's protocols. Briefly, after primary and secondary screening, positive plaques were picked and the phagemids were prepared by in vivo excision. The phagemids were transformed into XL1-Blue MRF cells. Clones were selected based on blue-white color selection of the colonies grown on LB-ampicillin agar plates. The plasmid harboring the cDNA inserts were then extracted using a plasmid DNA purification system (Cosmogenetech, Seoul, Korea). The cDNA inserts were then sequenced using the primer for T3 promotor (Cosmogenetech, DNA sequencing service, Seoul, Korea) and compared against the GenBank database.

Construction of recombinant TS-15-1, TS 15-1c domain and TS 15-1n domain
Following confirmation of the PCR product sequences, TS 15-1, The TS 15-1c (C-terminal serine protease domain) and TS 15-1n (N-terminal serine protease domain), the genes were ligated with pET-28a vector (Novagen, USA). After gene ligation, the constructed plasmids were expressed in Escherichia coli BL21 (DE3, Novagen, USA). Pre-cultured cells were inoculated into Luria-Bertani broth containing kanamycin, and the cells were grown at 37˚C until an OD 600 of 0.5-0.6 was reached. Recombinant TS 15-1N and TS 15-1C expressions were induced addition of 0.5 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) at 25˚C for 16 h. The cells were harvested by centrifugation and the cell pellets were resuspended in buffer. A consisting of 50 mM Tris-HCl pH 7.5 and 200 mM NaCl. Cell disruptions were lysed by sonication on ice and the crude extracts were centrifuged to remove the cell debris. Ts15-1 N and C pellets were then sonicated in buffer including 50 mM Tris-HCl pH 7.5, 200 mM NaCl, and 6 M Urea on ice. The clear supernatant of the lysate was subjected onto the Ni-NTA column which had been pre-equilibrated with buffer A. The column was subsequently washed with buffer A containing imidazole, after which the bound proteins were eluted by varying the imidazole concentration (20-400 mM). The eluted proteins were analyzed using 10% SDS-PAGE. However, we could not get recombinant protein of TS 15-1 because very poor expression level.

Production of polyclonal antisera for F3 fraction or TS 15-1c
Female four-week-old Wistar rats were purchased from Samtako Co. (Gyeonggi-do, Korea). Rats were immunized subcutaneously with a 1:1 mixture of the 250 μg F3 fraction of TS 15-1c protein (in 0.5 ml PBS) and 0.5 ml Freund's complete adjuvant (#F5881, Sigma-Aldrich, USA) at 0 week. At 2 weeks the rat was given additional infections of the 250 μg F3 fraction or TS 15-1c protein with Freund's incomplete adjuvant (#F5506, Sigma-Aldrich, USA). One week after their final booster, rats were sacrificed and serum was obtained.

Real-time PCR
Homogenized ear tissues were mixed with TRIzol (Invitrogen, Germany), and total RNA extraction and cDNA synthesis (Invitrogen, Germany) was performed in accordance with the manufacturer's protocols. Expression levels of several genes were determined with real-time RT-PCR using the iCycler (Bio-Rad laboratories Inc., USA) real-time PCR machine. Primer sequences for collagen I, TGF-β, smad2, smad3, and GAPDH, and PCR conditions were identical to those mentioned in the previous study [5]. Each gene expression levels were normalized with GAPDH gene expression.

Collection of serum
Mice were killed at 0, 1, 2, and 4 weeks after T. spiralis infection and serum was obtained. Sera were stored at -20˚C until used.

Immunofluorescence
Paraffin-embedded T. spiralis infected or non-infected mouse muscle tissue were de-paraffinized and hydrated. For antigen retrieval, slides were immersed in citrate buffer (0.01 M, pH 6.0) and heated twice in a microwave (700 W or 'high') for 5 min. Slides were then quenched with endogenous peroxidase by incubation in a 3% hydrogen peroxide solution for 5 min and were washed three times in PBS for 5 min each. Slides were immuno-stained with primary antibody (α-TS 15-1c antibody that was produced according to the polyclonal antisera method; 1:500 dilution) at 4˚C overnight. After primary antibody incubation, slides were washed three times in PBS for 5 min each and were incubated with secondary antibody, the Alexa Fluor 594 goat anti-rat IgG secondary antibody (1:500; Invitrogen, USA) was applied for 1 h at 24˚C. The slides were washed in PBS and mounted with Permount (Fisher Scientific, Pittsburgh, PA, USA). Confocal images of stained muscle tissue were examined under an inverted fluorescence microscope.

Statistical analysis
All experiments were performed three times for confirmation of statistical significance. Mean ± standard deviation (SD) was calculated from data collected from individual mice. Significant differences were determined using one-way or two-way analysis of variance. Statistical analysis was performed with GraphPad Prism 5.0 software (GraphPad Software Inc., CA, USA).

Ethics statement
The study was performed with approval from the Pusan National University Animal Care and Use Committee (IACUC protocol approval; PNU-2016-1175), in compliance with ''The Act for the Care and Use of Laboratory Animals" of the Ministry of Food and Drug Safety, Korea. All animal procedures were conducted in a specific pathogen-free facility at the Institute for Laboratory Animals of Pusan National University.

Type I collagen gene expression in an aging mouse model
In order to understand the collagen gene inducing effect of ES-P, transcription and protein expression levels of type I collagen and TGF-β1 signaling related proteins were compared in ear tissues of 6 and 14 week-old mice that had or had not received ES-P treatment (Fig 1A). The expression levels of the collagen I and TGF-β1 genes of the 14 week-old mice were significantly decreased compared to those of the 6 weeks mice. However, those of the ES-P treated 14 week-old mouse group were significantly increased compared to un-treated 14 week-old mice ( Fig 1B).

Fractionation of ES-P and evaluation of collagen gene induction of major fractions
To identify type I collagen inducing factors from the T. spiralis ES-P, the ES-P was fractionated to several fractions including three big fractions by gel filtration chromatography. The three major fractions obtained were named F1 (about 100 kDa-140 kDa), F2 (about 80 kDa-120 kDa), and F3 (about 50 kDa -90 kDa) respectively (Fig 2A). In order to determine which major fraction had collagen gene expression inducing factors, each fraction was used to treat MEF cells, and expression levels of the type I collagen gene were measured. After F1, F2, and F3 treatment, only F3 treated MEF cells had significantly increased type I collagen gene expression ( Fig 2B). Moreover, expression levels of collagen I in F3 treated MEFs was higher those of ES-P treated MEFs (Fig 2B).

Protein activity evaluation and size determine of F3
In order to determine whether the collagen inducing ability of F3 is related with serine protease activity, we evaluated the collagen inducing ability of F3 following pre-treatment with a serine protease inhibitor, PMSF, on MEF cells. The collagen I gene expression levels were significantly decreased in MEF cells pre-treated with PMSF, the serine protease inhibitor. In addition, the gene expression levels were also not increased when treated with boiled F3 (Fig 2C). In order to confirm the existence and expression levels of F3 in ES-P, α-F3 polyclonal antibody was used against ES-P and F3 in a western blot analysis. The presence of a strong band was observed at 60-80 kDa in both the ES-P and F3 samples (Fig 2D).

Immunoscreening of a cDNA library from T. spiralis muscle larva by α-F3 antibody
In order to identify the collagen gene inducing factors from T. spiralis ES-P, immunoscreening was conducted against the T. spiralis muscle larvae Express cDNA library with the α-F3 antibody. Thirty-five positive plaques were detected in primary screening, among them, 10 plaques were confirmed by second screening (S1 Fig). These plaques were amplified and processed in an in vivo excision step. All the insert DNA from the 10 positive clones were sequenced and their amino acid sequences were determined. Two insert DNA fragments (TS 15-1 and TS 15-2) were similar to a putative trypsin of T. spiralis with 90% identity. Another clone (TS 15-3) was matched to a nuclear receptor-binding protein of T. spiralis with 35% of identity. Another clone (TS-16-1) was matched to a putative BTB/POZ domain protein of T. spiralis with 63% identity. The remaining 6 insert clones were not matched with any previously known genes.

Molecular characterization of TS 15-1
Collagen inducing factors in ES-P and F3 had serine protease activity and were measured to be about 60-72 kDa in size. After evaluation of the size and serine protease activity of positive clone matched genes, the TS 15-1 gene was selected for downstream identification of the collagen inducing factor. The TS 15-1 fragment was 2,004 bp long and encoded a 667 amino acid protein, and the molecular weight and pI was calculated as 71.6 kDa and 8.83. The deduced TS 15-1 protein has two conserved catalytic motifs, an N-terminal Tryp_SPc domain (TS 15-1n) and a C-terminal Tryp_SPc domain (TS 15-1c) (Fig 3A). The TS 15-1n and TS 15-1c peptides were composed of 238 amino acids and 239 amino acids respectively, and the molecular weight was calculated to be 26.1 kDa and 26.2 kDa respectively. Unfortunately, collection of recombinant full length of TS-15 protein was very difficult because its expression level was very low. We conducted recombinant protein expression of the N and C terminal domains (about 26 kDa, Fig 3B) and evaluated their collagen gene inducing ability. collagen I expression levels in the recombinant TS 15-1c protein treated cells were significantly increased compared to a media control. However, recombinant TS 15-1n protein treated cells were not significantly changed compared to those of medium treated cells (Fig 3C). In order to know the protease activity of both recombinant proteins, zymogram analysis was conducted. A collagen digested clear zone was detected around~26 kDa in the recombinant TS 15-1c protein lane, but the clear zone was not detected with the recombinant TS 15-1n protein (Fig 3D).

Molecular structure of TS 15-1c & TS 15-1n
In this study, we determined a molecular model by homology modeling based on the structure of another serine protease (PDB ID : 1KYN, 1-235). In TS 15-1c (G342-T580), predictions of the active sites (H389, D444, and S533) and the substrate binding sites (G527, S553, and G555) are shown in blue and red letters, respectively (Fig 4A). Interestingly, these results indicated that these sites interact with inhibitors and ligands. Most residues in these regions had negative charges in a globular fold (Fig 4B). Surprisingly, both TS 15-1n and granzyme B structures were shown to have very similar folding patterns (S2 Fig). The TS 15-1n is approximately 35% homologous to granzyme B (21-247). We found TS-15-1c and TS 15-1n molecular 3D model was quite different each other.

Expression and localization of TS-15 in the T. spiralis life cycle
In order to determine when the Ts 15-1 mRNA was the most highly expressed in the T. spiralis life cycle, real-time PCR was performed on new born larvae, adult worms, muscle stage larvae of T. spiralis, and during the T. spiralis infection period (at 0, 7, 14, 28 days after infection). As the results show, the Ts 15-1 gene was the most highly expressed in muscle stage larvae, and its expression is also highly elevated 28 days after infection (Fig 5A). In order to know whether TS 15-1 was secreted from parasites, an α-TS 15-1c antibody was produced and was reacted with T. spiralis ES-P and total extract. The TS 15-1c antibody strongly reacted with proteins around 72 kDa in ES-P and slightly reacted with a total extract at the same size ( Fig 5B). Furthermore, to know whether TS 15-1c has antigenicity or not, T. spiralis infected mice sera (0, 1, 2, and 4 weeks after infection) were reacted with recombinant TS 15-1c protein (Fig 5C). rTS 15-1c most strongly reacted with mouse serum collected 4 weeks after infection. To know where TS 15-1 is secreted in the parasite, α-TS 15-1c antibody was reacted against serial sections of the T. spiralis infected muscle using immunohistochemical methods. α-TS 15-1c antibody strongly reacted with only the ladder shapes structure around the esophagus in muscle stage larvae that appear to be stichocytes (Fig 6).

Evaluation of the TS 15-1c protein type I collagen inducing ability
In order to know whether TS 15-1c had type I collagen elevating ability, we applied TS 15-1c to the ear skin of 6 week-and 14 week-old mice and evaluated the expression levels of collagen I, Smad2/3, and TGF-β1 (Fig 7A). All of the tested genes' expression levels, including the collagen I gene of the 14 week-old mice, were significantly lower than those in the 6 week-old mice. However, after 14 TS 15-1c treatments on 14 week-old mice, collagen I, Smad2/3, and TGF-β1 gene expression levels in these mice were significantly increased compared with nontreated mice of the same age (Fig 7B). We investigated protein levels of type I collagen, the phosphorylation form of Smad2/3, and levels of TGF-β1 in TS 15-1c treated 14 week-old mice and the protein levels were considerably recovered relative to those of the non-treated 14 week-old mice (Fig 7C).

Discussion
In this study, we identified the host collagen inducing factor from T. spiralis, named it TS 15-1, and confirmed its serine protease activity and ability to elevate type I collagen, TGF-βI, and related signal proteins (Smad2/3) on a transcriptional and protein level. In addition, we found that it was secreted outside the parasite and elicited specific antibody production from the host immune system. In a previous study, we revealed that the ES-P of T. spiralis could induce collagen production of host muscle tissue during the infection period, and that it was closely related with serine protease activity [5].
We can carefully suggest that TS 15-1 is one of the key collagen inducing factors in ES-P revealed in our previous study. Although we could not demonstrate that TS 15-1 is one of the key molecules in the collagen capsules around the nurse cell formation step, it might be one of the central factors for collagen capsule formation. This is because TS 15-1 gene expression level was the highest during the T. spiralis muscle larva stage and its specific antibodies could be detected in mouse serum from 1 week up to 4 weeks after a T. spiralis infection (Fig 5). During the nurse cell formation period (1 week-4 weeks), T. spiralis might strongly secrete TS 15-1 to induce collagen capsule synthesis by the host muscle cell.
Parasite secretory proteases might have important functions in modulating the interactions between parasites and hosts because of their particular roles in the invasion of host tissues, parasite nutrition, and evasion of host immune responses [9][10][11][12]. A trypsin-like serine protease of parasites could be involved in host immune regulation [13][14][15]. Serine proteases in nematodes are known to be involved in invasion into host cells and tissues and are likely to be important in molting. TS 15-1 was revealed to be a serine protease, trypsin like protein, because its activity was inhibited by PMSF ( Fig 2C) and it was composed two domains which were very similar but not identical to each other (Fig 3A). Several secreted serine proteases have been identified among T. spiralis ES proteins, including the 69 kDa putative serine protease TsSerP (two trypsin-like domains), the 45 kDa serine protease TspSP-1, and a 35.5 kDa serine protease [9,11,[16][17][18]. Most of these have strong antigenicity, specific antibodies for them are easily detected experimentally in infected animal sera, and they have one or two trypsin like domains [9, 11,  16]. Most secreted proteases could elevate their specific antibodies during nematodiasis [16,19]. Trap et al., reported the identification of the putative serine protease, TsSerP, isolated from the T. spiralis adult-newborn larvae stage. It has two trypsin-like serine protease domains flanking a hydrophilic domain, which is the same structure as TS 15-1. Immunohistochemistry analysis revealed that TsSerP was located on the inner layer of the cuticle and esophagus of the parasite, TS 15-1 was also detected on the inner layer of the cuticle and stichocytes in this study (Fig 6). These two serine proteases of T. spiralis might have similar functions, although the function of TsSerP was not clearly revealed [9].
In this study, it was revealed that TS 15-1 could elevate collagen expression via the TGF-β1 signaling pathway in host tissue of normal aged mice. Because, the recombinant TS 15-1c protein could elevate collagen I production and the TGF-βI signaling pathway related to Smad2/3 proteins (Fig 7). Type I collagen expression is closely related with the TGF-βI/Smad2/Smad3 signaling pathway [20][21][22]. This characteristic could be used for therapeutic effects including wound healing and cosmetic usefulness with wrinkle reduction. The various serine proteases may participate in physiological or pathological processes, like tissue repair, vascular remodeling, and wound healing, which depend on cell proliferation and migration [23,24]. Type I collagen is the major structural protein in the skin. Collagen destruction is thought to underlie Host collagen inducing factor the appearance of aged skin and changes resulting from chronic sun exposure [25]. Ultraviolet irradiation from the sun has deleterious effects on human skin including cancer, photo-aging, and intrinsic aging [26]. TGF-β/Smad pathway is the major regulator of collagen homeostasis and plays a crucial role in dermal fibrosis [27,28]. TGF-β is the most potent direct stimulator of collagen production. Moreover, TGF-β is central to the process of wound healing and fibrosis formation in skin [29,30]. It is well understood that activation of TGF-β signaling pathways stimulus the Smad family downstream via phosphorylation. Wound healing is a well-orchestrated process, where numerous factors are activated or inhibited in a sequence of steps [31]. Numerous signaling pathways are involved, among of them, the TGF-β1/Smad pathway is representative and well known to participate in the wound healing process [31]. Hozzein et al., suggested that topical application of propolis would promote the wound healing process by promoting TGF-β/Smad signaling, leading to increased expression of collagen type I [32]. The gradual loss of collagen in skin with aging results in wrinkles and other signs of skin aging [33]. The content of type I collagen, the major collagen in the skin and a marker of collagen synthesis, is deceased by 68% in old skin versus young skin, and cultured young fibroblasts synthesize more type I collagen than old cells [33]. In addition, a possible influence of collagen membrane on extracellular matrix synthesis was addressed using analysis of TGF-β1 and Smad2/3 complex [34,35].
In conclusion, we identified a host collagen inducing factor from ES-P using immune screening methods and demonstrated the molecular/genetic characteristics and function of TS 15-1c. Further study will be required to understand the detailed mechanisms for receptors in the host cells, and to identify the minimal structure that can induce collagen for cosmetic and medical purposes.
Supporting information S1 Fig. Result of immunoscreening of T. spiralis cDNA library by α-F3 antibody. After T. spiralis cDNA containing phages were mixed with E. coli, the plaques were incubated with NC membranes for 4 hrs. The membranes were reacted with α-F3 antibody (1:500) as the primary antibody and α-rat IgG antibody conjugated with HRP was reacted as secondary antibody. After adding of 3,3'-diaminobenzidine (DAB), colored spots were compared with original plates. Positive plaques were amplified and re-analyzed by the same method.