- Research article
- Open Access
Hepatocyte growth factor ameliorates dermal sclerosis in the tight-skin mouse model of scleroderma
Arthritis Research & Therapy volume 8, Article number: R161 (2006)
The tight-skin (TSK/+) mouse, a genetic model of systemic sclerosis (SSc), develops cutaneous fibrosis and defects in pulmonary architecture. Because hepatocyte growth factor (HGF) is an important mitogen and morphogen that contributes to the repair process after tissue injury, we investigated the role of HGF in cutaneous fibrosis and pulmonary architecture defects in SSc using TSK/+ mice. TSK/+ mice were injected in the gluteal muscle with either hemagglutinating virus of Japan (HVJ) liposomes containing 8 μg of a human HGF expression vector (HGF-HVJ liposomes) or a mock vector (untreated control). Gene transfer was repeated once weekly for 8 weeks. The effects of HGF gene transfection on the histopathology and expression of tumor growth factor (TGF)-β and IL-4 mRNA in TSK/+ mice were examined. The effect of recombinant HGF on IL-4 production by TSK/+ CD4+ T cells stimulated by allogeneic dendritic cells (DCs) in vitro was also examined. Histologic analysis revealed that HGF gene transfection in TSK/+ mice resulted in a marked reduction of hypodermal thickness, including the subcutaneous connective tissue layer. The hypodermal thickness of HGF-treated TSK/+ mice was decreased two-fold to three-fold compared with untreated TSK/+ mice. However, TSK/+ associated defects in pulmonary architecture were unaffected by HGF gene transfection. HGF gene transfection significantly inhibited the expression of IL-4 and TGF-β1 mRNA in the spleen and skin but not in the lung. We also performed a mixed lymphocyte culture and examined the effect of recombinant HGF on the generation of IL-4. Recombinant HGF significantly inhibited IL-4 production in TSK/+ CD4+ T cells stimulated by allogeneic DCs. HGF gene transfection inhibited IL-4 and TGF-β mRNA expression, which has been postulated to have a major role in fibrinogenesis and reduced hypodermal thickness, including the subcutaneous connective tissue layer of TSK/+ mice. HGF might represent a novel strategy for the treatment of SSc.
Systemic sclerosis (SSc) is a connective tissue disorder of unknown etiology that is characterized by an excessive deposition of extracellular matrix protein in the affected skin, in addition to various internal organs. Currently, no effective therapies for SSc exist . The tight-skin (TSK/+) mouse is a genetic model for human SSc. Although the phenotypic characteristics of the TSK/+ mouse are not identical to those of human SSc patients, TSK/+ mice produce autoantibodies against SSc-specific autoantigens, including topo-I, fibrillin 1 (fbn-1), collagen type 1, and Fcγ receptors [2, 3]. The gene defect responsible for the TSK/+ phenotype in mice is yet to be definitively identified; however, the fbn-1 gene has been recently proposed as a candidate locus for this disorder . The fbn-1 gene mutation seems to provide an explanation for the embryonic lethality of homozygous tight skin (TSK/TSK) animals. Heterozygous (TSK/+) mice, which have a normal lifespan, exhibit fibrosis and thickening of subcutaneous dermal tissue. Other abnormalities in TSK/+ mice include increased lung collagen content, enlarged air spaces reminiscent of pulmonary emphysema, and, with advanced age, development of progressive myocardial fibrosis and hypertrophy [5–7].
Hepatocyte growth factor (HGF) was originally identified and cloned as a potent mitogen for hepatocytes [8, 9]. It has mitogenic, motogenic, and morphogenic effects on various epithelial tissues, including the liver, kidneys, lungs, and intestines [10–12]. HGF also shows antiapoptotic activity  and has a role in suppressing fibrosis in the liver . HGF might, therefore, induce tissue repair in dermal sclerosis associated with SSc. We recently demonstrated that repeated transfection of the human HGF gene into skeletal muscle induced continuous production of HGF, strongly inhibited acute graft-versus-host disease (GVHD) after allogeneic hematopoietic stem-cell transplantation (HSCT), and protected against thymic damage caused by GVHD in a well-characterized mouse model of GVHD [15, 16]. The present study was performed to examine the therapeutic effect of HGF on tissue fibrosis in TSK/+ mice.
Materials and methods
TSK/+ and homozygous pallid (pa/pa) mutant mice with a C57BL/6 background were obtained from the Jackson Laboratory (Bar Harbor, ME, USA). TSK/+ mice are heterozygous for both TSK and pa gene mutations. TSK/+ mice were produced by mating TSK/+ male mice with pa/pa female mice. TSK/+ progeny were identified by their back-coat and eye colors, in addition to their characteristic loss of skin pliability. To verify the TSK/+ genotype, PCR amplification of a partially duplicated fbn-1 gene was carried out using genomic DNA from each mouse, as described previously . C57BL/6 and (C57BL/6 × DBA/2)F1 (BDF1) mice were obtained from the Shizuoka Laboratory Animal Center (Hamamatsu, Shizuoka, Japan). All mice were maintained in a pathogen-free facility at the Hyogo College of Medicine (Nishinomiya, Hyogo, Japan). Animal experiments were performed in accordance with the guidelines of the National Institutes of Health (Bethesda, MD, USA), as specified by the animal care policy of Hyogo College of Medicine.
Expression vector and preparation of liposomes containing hemagglutinating virus of Japan (HVJ)
Human HGF cDNA (2.2 kb) was inserted into the EcoRI and NotI sites of the pUC-SRα plasmid under control of the cytomegalovirus enhancer-promoter . HVJ liposomes containing plasmid DNA and high mobility group 1 protein were constructed, as described previously [15, 16]. Briefly, phosphatidylserine, phosphatidylcholine, and cholesterol were mixed at a weight ratio of 1 : 4.8 : 2. This lipid mixture (1 mg) plus plasmid DNA (20–40 μg), which had previously been complexed with 6–12 μg of high mobility group 1 nonhistone chromosomal protein purified from calf thymus, were sonicated to form liposomes and then mixed with ultraviolet-irradiated HVJ. Excess free virus was subsequently removed from the HVJ liposomes by sucrose-density-gradient centrifugation.
TSK/+ mice were injected in the gluteal muscle with either HVJ liposomes containing 8 μg of the human HGF expression vector (HGF-HVJ liposomes) or mock vector (untreated control). Gene transfer was repeated once weekly for 8 weeks.
Tissues were fixed in 10% buffered formalin and embedded in paraffin. Sections were stained with hematoxylin and eosin and were examined by light microscopy.
RNA was extracted using an Isogen (Nippongene, Toyama, Japan) kit, according to the manufacturer's instructions, and cDNA was prepared using 2.5 μM random hexamers (Applied Biosystems Inc., Foster City, CA, USA). IL-4 and TGF-β mRNA levels were quantified by real-time RT-PCR in a total volume of 25 μl for 40–50 cycles of 15 seconds at 95°C and 40–50 cycles of 1 minute at 60°C. Samples were run in triplicate and relative expression levels were determined by normalizing expression levels to that of β-actin. The primer sequences used were as follows:
1. IL-4, CCAGCTAGTTGTCATCCTGCTCTTCTTTCTCG and CAGTGATGAGGACTTGGACTCATTCATGGTGC.
2. TGF-β1, TGGACCGCAACAACGCCATCTATGAGAAAACC and TGGAGCTGAAGCAATAGTTGGTATCCAGGGCT.
3. β-actin, TGTGATGGTGGGAATGGGTCAG and TTTGATGTCACGCACGATTTCC.
Mixed lymphocyte reaction (MLR) and in-vitro cytokine production
CD4+ T cells and CD11c+ dendritic cells (DCs) were purified from spleen cells using immunomagnetic beads (Miltenyi Biotec, CA, USA). The purity of the CD4+ and CD11c+ cell populations was >90% and >95%, respectively. CD4+ T cells from TSK/+ (H-2b) mice (4 × 106 cells/ml/well) were cultured with irradiated (20 Gy) CD11c+ DCs from BDF1 (H-2b × d) mice (1 × 106 cells/ml/well) in 24-well flat-bottomed plates (Falcon Labware, Lincoln Park, NJ, USA). After 72 hours, viable cells (1 × 105 cells/200 μl/well) were stimulated in 96-well flat-bottomed plates (Falcon Labware) coated with 5 μg/ml anti-CD3 mAb. After 48 hours, IL-4 and IFN-γ concentrations in the culture supernatants were measured by ELISA.
ELISA for IL-4
The levels of murine IL-4 in culture supernatants were measured by ELISA using antimouse IL-4 mAb (Genzyme Pharmaceuticals, Cambridge, MA, USA) according to the manufacturer's protocol.
Group mean values were compared by the two-tailed Student's t-test. A p value of < 0.05 was considered statistically significant.
Prevention of scleroderma by HGFgene transfection
We previously reported that repeated transfection of the human HGF gene into skeletal muscle of allogeneic HSCT recipients reduced the tissue damage and subsequent inflammatory responses caused by acute GVHD [15, 16]. To investigate the possible therapeutic effects of HGF on SSc, young TSK/+ mice were treated with HGF gene transfection. Treatment consisted of once-weekly intramuscular injection of either HGF-HVJ liposomes or control mock vectors for a period of 8 weeks (Figure 1). Histologic analysis revealed that HGF treatment of TSK/+ mice resulted in a marked reduction of hypodermal thickness, including the subcutaneous connective tissue layer (Figure 2). Skin fibrosis was assessed quantitatively by measuring hypodermal thickness. The hypodermal thickness of HGF-treated TSK/+ mice was decreased two-fold to three-fold compared with untreated TSK/+ mice (Figure 3).
Effect of HGFgene transfection on pulmonary changes
The effect of HGF gene transfection on pulmonary changes was examined. Control mock-vector-transfected TSK/+ mice all displayed a markedly dilated alveolar space, with fewer alveolar walls compared with pa/pa mice. This TSK/+-associated abnormality in lung architecture was unaffected by HGF gene transfection (Figure 4).
Effect of HGF on the expression of IL-4 and TGF-β mRNA expression and production
IL-4 and TGF-β have been postulated to have major roles in fibrinogenesis in animal models [19–23]. To clarify whether modulation of IL-4 and TGF-β has a role in the prevention of sclerosis induced by HGF gene transfection in the scleroderma model mouse, we examined the mRNA expression of these cytokines. HGF gene transfection significantly inhibited the expression of IL-4 and TGF-β1 mRNA in the spleen and skin but not in the lung (Figure 5). We also performed MLR and examined the effect of HGF on the production of IL-4. Responder CD4+ T cells from TSK/+ mice were cultured with irradiated (20 Gy) CD11c+ DCs from BDF1 mice with or without recombinant HGF. After 3 days' culture, viable cells were stimulated by culture with anti-CD3 mAb for 48 hours and the IL-4 level in the culture supernatant was assayed by ELISA. HGF significantly inhibited IL-4 production from TSK/+ CD4+ T cells stimulated by BDF1 DCs (Figure 6).
SSc is an autoimmune connective tissue disease that is characterized by microvascular damage, extracellular matrix deposition, and fibrosis. There is no completely effective treatment for this disease at present. We previously demonstrated that serum HGF levels were significantly elevated in patients with SSc and serum HGF levels correlated to markers of endothelial injury (thrombomodulin) and interstitial lung injury (KL-6), suggesting that elevation of serum HGF counteracts the endothelial and interstitial lung injury caused by SSc . The serum level of HGF is significantly elevated in various diseases, depending on the severity of the disease [25–27]. However, endogenously induced HGF is not sufficient to repair tissue injuries, and, therefore, supplementation with exogenous HGF is necessary to accelerate the tissue repair process in animal models [14, 15, 28]. In the present study, we assessed the effect of exogenous HGF on skin fibrosis and the development of pulmonary defects in the TSK/+ mouse model of SSc. Both our present study and other previous studies  have shown that dermal thickness is similar in TSK/+ and wild-type littermates, but hypodermal thickness, including the subcutaneous connective tissue layer, is significantly increased in TSK/+ mice compared with wild-type littermates. HGF gene transfection of TSK/+ mice for a period of 8 weeks resulted in a marked reduction of hypodermal thickness, including the subcutaneous connective tissue layer. Although the therapeutic effect of HGF is not significant, we also observed the reduction of hypodermal thickness in TSK/+ mice following HGF gene transfection for a period of 4 weeks (data not shown).
Although the cause of SSc is unknown, IL-4 and TGF-β have been postulated to have major roles in fibrinogenesis. In one study, intravenously administered human immunoglobulin decreased splenocyte secretion of IL-4 and TGF-β, which resulted in abrogation of fibrinogenesis in TSK/+ mice and, consequently, prevented the accumulation of fibrous tissue . Furthermore, administration of an anti-IL-4 or anti-TGF-β antibody prevented dermal collagen deposition in TSK/+ mice and murine sclerodermatous GVHD, respectively [20, 21]. In the present study, HGF treatment also reduced expression of both IL-4 and TGF-β mRNA in the spleen and skin.
IL-4 regulates collagen and extracellular matrix production by fibroblasts [22, 23]. TSK/+ mice exhibiting disrupted genes encoding IL-4 receptor alpha (IL-4Rα) or IL-4 lacked skin sclerosis [17, 29], suggesting that IL-4 has a crucial role in skin sclerosis in TSK/+ mice. A primary source of IL-4 in vivo is CD4+ T cells  and a previous study demonstrated that CD4+ T cells were essential to the TSK/+ phenotype, because a lack of these cells prevented development of dermal thickening . Therefore, we examined the effect of HGF on the generation of IL-4 from CD4+ T cells. HGF significantly inhibited IL-4 production from CD4+ T cells stimulated by allogeneic DCs, suggesting that HGF inhibits dermal fibrosis, in part, by inhibiting IL-4 production by CD4+ T cells.
We also observed downregulation of TGF-β1 mRNA expression in TSK/+ mice by HGF gene transfection. TGF-β1 has a role in the induction of fibrosis, and HGF gene transfection inhibited the production of TGF-β1 from macrophage-like cells and fibroblastic cells . Downregulation of TGF-β1 expression and inhibition of fibrosis by HGF were noted in a rat model of liver cirrhosis  and a mouse model of chronic renal failure . Recently, HGF has been shown to downregulate TGF-β1 expression and prevent dermal sclerosis in a murine bleomycin-induced scleroderma model . The authors observed that HGF gene transfection significantly reduced both the expression of TGF-β1 mRNA and the production of TGF-β1 by fibroblastic cells and macrophage-like cells that infiltrated the dermis. Furthermore, HGF gene transfection prevented the symptoms of not only dermal sclerosis, but also lung fibrosis induced by bleomycin injection.
By contrast, HGF gene transfection failed to alter the development of pulmonary abnormalities in TSK/+ mice in our study. The pathologic alteration of the lung structure of TSK/+ mice represents pulmonary emphysema and is not related to hypersynthesis of collagen that is similar to the pulmonary fibrosis associated with SSc . Apparently, emphysema in TSK/+ mice is not owing to the mutated fbn-1 gene that is responsible for the occurrence of cutaneous hyperplasia, because transgenic mice bearing a mutated fbn-1 gene developed cutaneous hyperplasia but did not exhibit pulmonary emphysema . Furthermore, TSK/+ mice exhibiting disrupted genes encoding IL-4Rα, TGF-β, or IL-4 lacked skin sclerosis but developed emphysema, indicating that different genes are involved in the development of skin sclerosis and pulmonary emphysema in TSK/+ mice [17, 29]. Furthermore, other studies have shown that the pulmonary pathology remained unchanged in TSK/+ CD4 knockout (CD4-/-) mice  and TSK/+ mice treated with an anti-IL-4 antibody . The dermal and pulmonary components of the TSK/+ phenotype can, therefore, be dissociated in vivo.
We used a transgenic approach instead of using a recombinant protein for the following reasons:
1. Because the half-life of a recombinant protein is quite short, recombinant protein treatment needs an enormous dose of the active form of HGF protein and frequent injections.
2. Administering a high dose of the active form of the HGF protein could cause adverse effects, such as tumorigenesis in other organs .
3. Recombinant protein treatment is very costly.
By contrast, the transgenic approach is simple, safe, and cheap and needs much less frequent injections. Repeated weekly injection of HGF-HVJ liposomes achieves a continuous high plasma level of HGF [14–16].
Although further studies are needed to fully explore the effects of HGF on SSc, it is possible that HGF therapy might be a promising strategy for the treatment of SSc.
HGF gene transfection of TSK/+ mice resulted in a marked reduction of hypodermal thickness, including the subcutaneous connective tissue layer. However, TSK/+-associated defects in pulmonary architecture were unaffected by HGF gene transfection. HGF gene transfection significantly inhibited the expression of IL-4 and TGF-β1 mRNA in the spleen and skin but not in the lung. Recombinant HGF significantly inhibited IL-4 production by TSK/+ CD4+ T cells stimulated by allogeneic DCs. HGF might represent a novel strategy for the treatment of SSc.
= CD4 knockout
= dendritic cell
= enzyme-linked immunosorbent assay
= fibrillin 1
= graft-versus-host disease
= hepatocyte growth factor
= hematopoietic stem-cell transplantation
= hemagglutinating virus of Japan
- IL-4 receptor alpha:
= monoclonal antibody
= mixed lymphocyte reaction
= homozygous pallid
= polymerase chain reaction
= reverse transcriptase
= systemic sclerosis
= tumor growth factor
= homozygous tight skin
= tight skin.
LeRoy EC: A brief overview of the pathogenesis of scleroderma (systemic sclerosis). Ann Rheum Dis. 1992, 51: 286-288.
Bona C, Rothfield N: Autoantibodies in scleroderma and tight skin mice. Curr Opin Immunol. 1994, 6: 931-937. 10.1016/0952-7915(94)90016-7.
Tan FK, Arnett FC, Antohi S, Saito S, Mirarchi A, Spiera H, Sasaki T, Shoichi O, Takeuchi K, Pandey JP, et al: Autoantibodies to the extracellular matrix microfibrillar protein, fibrillin-1, in patients with scleroderma and other connective tissue diseases. J Immunol. 1999, 163: 1066-1072.
Siracusa LD, McGrath R, Ma Q, Moskow JJ, Manne J, Christner PJ, Buchberg AM, Jimenez SA: A tandem duplication with the fibrillin 1 gene is associated with the mouse tight skin mutation. Genome Res. 1996, 6: 300-313.
Green MC, Sweet HO, Bunker LE: Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol. 1976, 82: 493-507.
Szapiel SV, Fulmer JD, Hunninghake GW, Elson NA, Kawanami O, Ferrans VJ, Crystal RG, et al: Hereditary emphysema in the tight-skin (Tsk/+) mouse. Am Rev Respir Dis. 1981, 123: 680-685.
Osborn TG, Bashey RI, Moore TL, Fischer VW: Collagenous abnormalities in the heart of the tight-skin mouse. J Mol Cell Cardiol. 1987, 19: 581-587. 10.1016/S0022-2828(87)80363-2.
Gohda E, Tsubouchi H, Nakayama H, Hirono S, Sakiyama O, Takahashi K, Miyazaki H, Hashimoto S, Daikuhara Y: Purification and partial characterization of hepatocyte growth factor from plasma of patient with fulminant hepatic failure. J Clin Invest. 1988, 81: 414-419.
Miyazawa K, Tsubouchi H, Naka D, Takahashi K, Okigaki M, Arakaki N, Nakayama H, Hirono S, Sakiyama O, Takahashi K, et al: Molecular cloning and sequence analysis of cDNA for human hepatocyte growth factor. Biochem Biophys Res Commun. 1989, 163: 967-973. 10.1016/0006-291X(89)92316-4.
Zarnegar R, Michalopoulos GK: The many faces of hepatocyte growth factor: from hepatopoiesis to hematopoiesis. J Cell Biol. 1995, 129: 1177-1180. 10.1083/jcb.129.5.1177.
Matsumoto K, Nakamura T: Hepatocyte growth factor (HGF) as a tissue organizer for organogenesis and regeneration. Biochem Biophys Res Commun. 1997, 239: 639-644. 10.1006/bbrc.1997.7517.
Kato Y, Yu D, Lukish JR, Schwartz MZ: Influence of luminar hepatocyte growth factor on small intestine mucosa in vivo. J Surg Res. 1997, 71: 49-53. 10.1006/jsre.1997.5136.
Bardelli A, Longati P, Albero D, Goruppi S, Schneider C, Ponzetto C, Comoglio PM: HGF receptor associates with anti-apoptotic protein BAG-1 and prevents cell death. EMBO J. 1996, 15: 6205-6212.
Ueki T, Kaneda Y, Tsutsui H, Nakanishi K, Sawa Y, Morishita R, Matsumoto K, Nakamura T, Takahashi H, Okamoto E, et al: Hepatocyte growth factor gene therapy of liver cirrhosis in rats. Nat Med. 1999, 5: 226-230. 10.1038/5593.
Kuroiwa T, Kakishita E, Hamano T, Kataoka Y, Seto Y, Iwata N, Kaneda Y, Matsumoto K, Nakamura T, Ueki T, et al: Hepatocyte growth factor ameliorates acute graft-versus-host disease and promotes hematopoietic function. J Clin Invest. 2001, 107: 1365-1373.
Imado T, Iwasaki T, Kataoka Y, Kuroiwa T, Hara H, Fujimoto J, Sano H: Hepatocyte growth factor preserves graft-versus-leukemia effect and T-cell reconstitution after marrow transplantation. Blood. 2004, 104: 1542-1549. 10.1182/blood-2003-12-4309.
McGaha T, Saito S, Phelps RG, Gordon R, Noben-Trauth N, Paul WE, Bona C: Lack of skin fibrosis in tight skin (TSK) mice with targeted mutation in the interleukin-4R alpha and transforming growth factor-beta genes. J Invest Dermatol. 2001, 116: 136-143. 10.1046/j.1523-1747.2001.00217.x.
Yaekashiwa M, Nakayama S, Ohnuma K, Sakai T, Abe T, Satoh K, Matsumoto K, Nakamura T, Takahashi T, Nukiwa T: Simultaneous or delayed administration of hepatocyte growth factor equally represses the fibrotic changes in murine lung injury induced by bleomycin. A morphologic study. Am J Respir Crit Care Med. 1997, 156: 1937-1944.
Blank M, Levy Y, Amital H, Shoenfeld Y, Pines M, Genima O: The role of intravenous immunoglobulin therapy in mediating skin fibrosis in tight skin mice. Arthritis Rheum. 2002, 46: 1689-1690. 10.1002/art.10363.
Ong C, Wong C, Roberts CR, Teh HS, Jirik FR: Anti-IL-4 treatment prevents dermal collagen deposition in the tight-skin mouse model of scleroderma. Eur J Immunol. 1998, 28: 2619-2629. 10.1002/(SICI)1521-4141(199809)28:09<2619::AID-IMMU2619>3.0.CO;2-M.
McCormick LL, Zhang Y, Tootell E, Gilliam AC: Anti-TGF-beta treatment prevents skin and lung fibrosis in murine sclerodermatous graft-versus-host disease: a model of human scleroderma. J Immunol. 1999, 163: 5693-5699.
Gillery P, Fertin C, Nicolas JF, Chastang B, Kalis B, Banchereau J, Maquart FX: Interleukin-4 stimulates collagen gene expression in human fibroblast monolayer culture. FEBS Lett. 1992, 302: 231-234. 10.1016/0014-5793(92)80448-P.
Postlethwaite AE, Holness MA, Katai H, Raghow R: Human fibroblasts synthesize elevated levels of extracellular matrix proteins in response to interleukin 4. J Clin Invest. 1992, 90: 1479-1485.
Hashimoto N, Iwasaki T, Kitano M, Ogata A, Hamano T: Levels of vascular endothelial growth factor and hepatocyte growth factor in sera of patients with rheumatic diseases. Mod Rheumatol. 2003, 13: 129-134.
Nakamura S, Moriguchi A, Morishita R, Aoki M, Yo Y, Hayashi S, Nakano N, Katsuya T, Nakata S, Takami S, et al: A novel vascular modulator, hepatocyte growth factor (HGF), as a potent index of the severity of hypertension. Biochem Biophys Res Commun. 1998, 242: 238-243. 10.1006/bbrc.1997.7800.
Shiota G, Okano J, Kawasaki H, Kawamoto T, Nakamura T: Serum hepatocyte growth factor levels in liver diseases: clinical implications. Hepatology. 1995, 21: 106-112. 10.1016/0270-9139(95)90416-6.
Okamoto T, Takatsuka H, Fujimori Y, Wada H, Iwasaki T, Kakishita E: Increased hepatocyte growth factor in serum in acute graft-versus-host disease. Bone Marrow Transplant. 2001, 28: 197-200. 10.1038/sj.bmt.1703095.
Ono M, Sawa Y, Mizuno S, Fukushima N, Ichikawa H, Bessho K, Nakamura T, Matsuda H: Hepatocyte growth factor suppresses vascular medial hyperplasia and matrix accumulation in advanced pulmonary hypertension of rats. Circulation. 2004, 110: 2896-2902. 10.1161/01.CIR.0000146342.30470.30.
Kodera T, McGaha TL, Phelps R, Paul WE, Bona CA: Disrupting IL-4 gene rescues mice homozygous for the tight-skin mutation from embryonic death and diminishs TGF-beta production by fibroblasts. Proc Natl Acad Sci USA. 2002, 99: 3800-3805. 10.1073/pnas.052709999.
Paul WE, Seder RA: Lymphocyte responses and cytokines. Cell. 1994, 76: 241-251. 10.1016/0092-8674(94)90332-8.
Wallace VA, Kondo S, Kono T, Xing Z, Timms E, Furlonger C, Keystone E, Gauldie J, Sauder DN, Mak TW, et al: A role of CD4+ T cells in the pathogenesis of skin fibrosis in tight skin mice. Eur J Immunol. 1994, 24: 1463-1466.
Mizuno S, Matsumoto K, Kurosawa T, Nakamura T: Reciprocal balance of hepatocyte growth factor and transforming growth factor-beta1 in renal fibrosis in mice. Kidney Int. 2000, 57: 937-948.
Mizuno S, Kurosawa T, Matsumoto K, Mizuno-Horikawa Y, Okamoto M, Nakamura T: Hepatocyte growth factor prevents renal fibrosis and dysfunction in a mouse model of chronic renal disease. J Clin Invest. 1998, 101: 1827-1834.
Wu MH, Yokozeki H, Tagawa S, Yamamoto T, Satoh T, Kaneda Y, Katayama I, Nishioka K: Hepatocyte growth factor prevents and ameliorates the symptoms of dermal sclerosis in a mouse model of scleroderma. Gene Therapy. 2004, 11: 170-180. 10.1038/sj.gt.3302165.
Rossi GA, Hunninghake GW, Gadek JE, Szapiel SU, Kawanami O, Ferons VJ, Crystal RG: Hereditary emphysema in tight skin mice. Am Rev Respir Dis. 1984, 129: 850-855.
Saito S, Nishimura H, Phelps RG, Wolf I, Miato S, Honjo T, Bona CA: Induction of skin fibrosis in expressing mutated Fibrillin-1 gene. Mol Med. 2000, 6: 825-836.
Takayama H, LaRochelle WJ, Sharp R, Otsuka T, Kriebel P, Anver M, Aaronson SA, Merlino G: Diverse tumorigenesis associated with aberrant development in mice overexpressing hepatocyte growth factor/scatter factor. Proc Natl Acad Sci USA. 1997, 94: 701-706. 10.1073/pnas.94.2.701.
T Iwasaki acknowledges the support of a Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture of Japan (No. 15591071).
The authors declare that they have no competing interests.
T Iwasaki conceived the study, participated in the design and co-ordination of the study, and participated in the interpretation of the results. T Imado and SK performed the animal study and histologic analysis. HS participated in the design of the animal study.
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Iwasaki, T., Imado, T., Kitano, S. et al. Hepatocyte growth factor ameliorates dermal sclerosis in the tight-skin mouse model of scleroderma. Arthritis Res Ther 8, R161 (2006). https://doi.org/10.1186/ar2068
- Hepatocyte Growth Factor
- Pulmonary Emphysema
- Serum Hepatocyte Growth Factor
- Human Hepatocyte Growth Factor
- Hepatocyte Growth Factor Gene