Publication Cover
Inhalation Toxicology
International Forum for Respiratory Research
Volume 25, 2013 - Issue 14
185
Views
17
CrossRef citations to date
0
Altmetric
Research Article

Asbestos-associated mesothelial cell autoantibodies promote collagen deposition in vitro

, , &
Pages 774-784 | Received 03 Aug 2013, Accepted 20 Sep 2013, Published online: 04 Dec 2013

References

  • Antony VB, Hott JW, Kunkel SL, et al. (1995). Pleural mesothelial cell expression of C-C (monocyte chemotactic peptide) and C-X-C (interleukin 8) chemokines. Am J Respir Cell Mol Biol 12:581–8
  • Bandli BR, Gunter ME. (2006). A review of scientific literature examining the mining history, geology, mineralogy, and amphibole asbestos health effects of the Rainy Creek igneous complex, Libby, Montana, USA. Inhal Toxicol 18:949–62
  • Baroni SS, Santillo M, Bevilacqua F, et al. (2006). Stimulatory autoantibodies to the PDGF receptor in systemic sclerosis. N Engl J Med 354:2667–76
  • Boylan AM, Ruegg C, Kim KJ, et al. (1992). Evidence of a role for mesothelial cell-derived interleukin 8 in the pathogenesis of asbestos-induced pleurisy in rabbits. J Clin Invest 89:1257–67
  • Chizzolini C, Raschi E, Rezzonico R, et al. (2002). Autoantibodies to fibroblasts induce a proadhesive and proinflammatory fibroblast phenotype in patients with systemic sclerosis. Arthritis Rheum 46:1602–13
  • Chlenski A, Guerrero LJ, Salwen HR, et al. (2011). Secreted protein acidic and rich in cysteine is a matrix scavenger chaperone. PLoS One 6:e23880
  • Cooper A. (1970). Thermodynamic studies of the assembly in vitro of native collagen fibrils. Biochem J 118:355–65
  • Dai J, Gilks B, Price K, Churg A. (1998). Mineral dusts directly induce epithelial and interstitial fibrogenic mediators and matrix components in the airway wall. Am J Respir Crit Care Med 158:1907–13
  • Dancer RC, Wood AM, Thickett DR. (2011). Metalloproteinases in idiopathic pulmonary fibrosis. Eur Respir J 38:1461–7
  • Davila RM, Crouch EC. (1993). Role of mesothelial and submesothelial stromal cells in matrix remodeling following pleural injury. Am J Pathol 142:547–55
  • Del Papa N, Conforti G, Gambini D, et al. (1994). Characterization of the endothelial surface proteins recognized by anti-endothelial antibodies in primary and secondary autoimmune vasculitis. Clin Immunol Immunopathol 70:211–16
  • Fineschi S, Goffin L, Rezzonico R, et al. (2008). Antifibroblast antibodies in systemic sclerosis induce fibroblasts to produce profibrotic chemokines, with partial exploitation of toll-like receptor 4. Arthritis Rheum 58:3913–23
  • Gabrielli A, Svegliati S, Moroncini G, et al. (2007). Stimulatory autoantibodies to the PDGF receptor: a link to fibrosis in scleroderma and a pathway for novel therapeutic targets. Autoimmun Rev 7:121–6
  • Garcia-Prieto E, Gonzalez-Lopez A, Cabrera S, et al. (2010). Resistance to bleomycin-induced lung fibrosis in MMP-8 deficient mice is mediated by interleukin-10. PLoS One 5:e13242
  • Goldblum SE, Ding X, Funk SE, Sage EH. (1994). SPARC (secreted protein acidic and rich in cysteine) regulates endothelial cell shape and barrier function. Proc Natl Acad Sci U S A 91:3448–52
  • Griffith DE, Miller EJ, Gray LD, et al. (1994). Interleukin-1-mediated release of interleukin-8 by asbestos-stimulated human pleural mesothelial cells. Am J Respir Cell Mol Biol 10:245–52
  • Guarino M, Tosoni A, Nebuloni M. (2009). Direct contribution of epithelium to organ fibrosis: epithelial-mesenchymal transition. Hum Pathol 40:1365–76
  • Guo H, Leung JC, Chan LY, et al. (2004). The pathogenetic role of immunoglobulin G from patients with systemic lupus erythematosus in the development of lupus pleuritis. Rheumatology (Oxford) 43:286–93
  • Harris BS, Zhang Y, Card L, et al. (2011). SPARC regulates collagen interaction with cardiac fibroblast cell surfaces. Am J Physiol Heart Circ Physiol 301:H841–7
  • Harvey W, Amlot PL. (1983). Collagen production by human mesothelial cells in vitro. J Pathol 139:337–47
  • Hashimoto N, Phan SH, Imaizumi K, et al. (2010). Endothelial-mesenchymal transition in bleomycin-induced pulmonary fibrosis. Am J Respir Cell Mol Biol 43:161–72
  • Hedenborg M, Sorsa T, Lauhio A, Klockars M. (1990). Asbestos fibers induce release of collagenase by human polymorphonuclear leukocytes. Immunol Lett 26:25–9
  • Hinz B, Phan SH, Thannickal VJ, et al. (2007). The myofibroblast: one function, multiple origins. Am J Pathol 170:1807–16
  • Ihn H, Sato S, Fujimoto M, et al. (2000). Characterization of autoantibodies to endothelial cells in systemic sclerosis (SSc): association with pulmonary fibrosis. Clin Exp Immunol 119:203–9
  • Iruela-Arispe ML, Vernon RB, Wu H, et al. (1996). Type I collagen-deficient Mov-13 mice do not retain SPARC in the extracellular matrix: implications for fibroblast function. Dev Dyn 207:171–83
  • Kamp DW. (2009). Asbestos-induced lung diseases: an update. Transl Res 153:143–52
  • Kuwahara M, Kuwahara M, Verma K, et al. (1994). Asbestos exposure stimulates pleural mesothelial cells to secrete the fibroblast chemoattractant, fibronectin. Am J Respir Cell Mol Biol 10:167–76
  • Lange A. (1980). An epidemiological survey of immunological abnormalities in asbestos workers. II. Serum immunoglobulin levels. Environ Res 22:176–83
  • Larson TC, Meyer CA, Kapil V, et al. (2010). Workers with Libby amphibole exposure: retrospective identification and progression of radiographic changes. Radiology 255:924–33
  • Liu JY, Brody AR. (2001). Increased TGF-beta1 in the lungs of asbestos-exposed rats and mice: reduced expression in TNF-alpha receptor knockout mice. J Environ Pathol Toxicol Oncol 20:97–108
  • Liu JY, Morris GF, Lei WH, et al. (1996). Up-regulated expression of transforming growth factor-alpha in the bronchiolar-alveolar duct regions of asbestos-exposed rats. Am J Pathol 149:205–17
  • Liu Q, Mao H, Nie J, et al. (2008). Transforming growth factor {beta}1 induces epithelial-mesenchymal transition by activating the JNK-Smad3 pathway in rat peritoneal mesothelial cells. Perit Dial Int 28:S88–95
  • Marchand LS, St-Hilaire S, Putnam EA, et al. (2012). Mesothelial cell and anti-nuclear autoantibodies associated with pleural abnormalities in an asbestos exposed population of Libby MT. Toxicol Lett 208:168–73
  • Martinek N, Shahab J, Sodek J, Ringuette M. (2007). Is SPARC an evolutionarily conserved collagen chaperone? J Dent Res 86:296–305
  • May JV, Frost JP, Schomberg DW. (1988). Differential effects of epidermal growth factor, somatomedin-C/insulin-like growth factor I, and transforming growth factor-beta on porcine granulosa cell deoxyribonucleic acid synthesis and cell proliferation. Endocrinology 123:168–79
  • Nasreen N, Mohammed KA, Mubarak KK, et al. (2009). Pleural mesothelial cell transformation into myofibroblasts and haptotactic migration in response to TGF-beta1 in vitro. Am J Physiol Lung Cell Mol Physiol 297:L115–24
  • Nigam SK, Suthar AM, Patel MM, et al. (1993). Humoral immunological profile of workers exposed to asbestos in asbestos mines. Indian J Med Res 98:274–7
  • Noonan CW, Pfau JC, Larson TC, Spence MR. (2006). Nested case-control study of autoimmune disease in an asbestos-exposed population. Environ Health Perspect 114:1243–7
  • Oh CK, Ariue B, Alban RF, et al. (2002). PAI-1 promotes extracellular matrix deposition in the airways of a murine asthma model. Biochem Biophys Res Commun 294:1155–60
  • Parsons CJ, Takashima M, Rippe RA. (2007). Molecular mechanisms of hepatic fibrogenesis. J Gastroenterol Hepatol 22(Suppl. 1):S79–84
  • Peipins LA, Lewin M, Campolucci S, et al. (2003). Radiographic abnormalities and exposure to asbestos-contaminated vermiculite in the community of Libby, Montana, USA. Environ Health Perspect 111:1753–9
  • Pershouse MA, Smartt AM, Schwanke C, Putnam EA. (2009). Differences in gene expression profiles from asbestos-treated SPARC-null and wild-type mouse lungs. Genomics 94:101–9
  • Pfau JC, Li S, Holland S, Sentissi JJ. (2011). Alteration of fibroblast phenotype by asbestos-induced autoantibodies. J Immunotoxicol 8:159–69
  • Pfau JC, Sentissi JJ, Weller G, Putnam EA. (2005). Assessment of autoimmune responses associated with asbestos exposure in Libby, Montana, USA. Environ Health Perspect 113:25–30
  • Phan SH. (2002). The myofibroblast in pulmonary fibrosis. Chest 122:286S–9S
  • Phan SH. (2008). Biology of fibroblasts and myofibroblasts. Proc Am Thorac Soc 5:334–7
  • Piera-Velazquez S, Li Z, Jimenez SA. (2011). Role of endothelial-mesenchymal transition (EndoMT) in the pathogenesis of fibrotic disorders. Am J Pathol 179:1074–80
  • Renaudineau Y, Revelen R, Levy Y, et al. (1999). Anti-endothelial cell antibodies in systemic sclerosis. Clin Diagn Lab Immunol 6:156–60
  • Rentz TJ, Poobalarahi F, Bornstein P, et al. (2007). SPARC regulates processing of procollagen I and collagen fibrillogenesis in dermal fibroblasts. J Biol Chem 282:22062–71
  • Rohs AM, Lockey JE, Dunning KK, et al. (2008). Low-level fiber-induced radiographic changes caused by Libby vermiculite: a 25-year follow-up study. Am J Respir Crit Care Med 177:630–7
  • Sage H, Decker J, Funk S, Chow M. (1989a). SPARC: a Ca2+-binding extracellular protein associated with endothelial cell injury and proliferation. J Mol Cell Cardiol 21:13–22
  • Sage H, Vernon RB, Decker J, et al. (1989b). Distribution of the calcium-binding protein SPARC in tissues of embryonic and adult mice. J Histochem Cytochem 37:819–29
  • Scabilloni JF, Wang L, Antonini JM, et al. (2005). Matrix metalloproteinase induction in fibrosis and fibrotic nodule formation due to silica inhalation. Am J Physiol Lung Cell Mol Physiol 288:L709–17
  • Siegel RC. (1976). Collagen cross-linking. Synthesis of collagen cross-links in vitro with highly purified lysyl oxidase. J Biol Chem 251:5786–92
  • Strandjord TP, Madtes DK, Weiss DJ, Sage EH. (1999). Collagen accumulation is decreased in SPARC-null mice with bleomycin-induced pulmonary fibrosis. Am J Physiol 277:L628–35
  • Sullivan PA. (2007). Vermiculite, respiratory disease, and asbestos exposure in Libby, Montana: update of a cohort mortality study. Environ Health Perspect 115:579–85
  • Sung HJ, Johnson CE, Lessner SM, et al. (2005). Matrix metalloproteinase 9 facilitates collagen remodeling and angiogenesis for vascular constructs. Tissue Eng 11:267–76
  • Tamura M, Liang D, Tokuyama T, et al. (1993). Study on the relationship between appearance of autoantibodies and chest X-ray findings of asbestos plant employees. Sangyo Igaku 35:406–12
  • Tamura M, Tokuyama T, Kasuga H, et al. (1996). Study on correlation between chest X-P course findings and change in antinuclear antibody in asbestos plant employees. Sangyo Eiseigaku Zasshi 38:138–41
  • Tan RJ, Fattman CL, Niehouse LM, et al. (2006). Matrix metalloproteinases promote inflammation and fibrosis in asbestos-induced lung injury in mice. Am J Respir Cell Mol Biol 35:289–97
  • Wang JC, Lai S, Guo X, et al. (2010). Attenuation of fibrosis in vitro and in vivo with SPARC siRNA. Arthritis Res Ther 12:R60 . doi:10.1186/ar2973
  • Whitehouse AC. (2004). Asbestos-related pleural disease due to tremolite associated with progressive loss of lung function: serial observations in 123 miners, family members, and residents of Libby, Montana. Am J Ind Med 46:219–25
  • Whitehouse AC, Black CB, Heppe MS, et al. (2008). Environmental exposure to Libby Asbestos and mesotheliomas. Am J Ind Med 51:877–80
  • Willis BC, Liebler JM, Luby-Phelps K, et al. (2005). Induction of epithelial-mesenchymal transition in alveolar epithelial cells by transforming growth factor-beta1: potential role in idiopathic pulmonary fibrosis. Am J Pathol 166:1321–32
  • Wynn TA. (2007). Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases. J Clin Invest 117:524–9
  • Wynn TA. (2008). Cellular and molecular mechanisms of fibrosis. J Pathol 214:199–210
  • Zavadil J, Bottinger EP. (2005). TGF-beta and epithelial-to-mesenchymal transitions. Oncogene 24:5764–74
  • Zhang HY, Gharaee-Kermani M, Zhang K, et al. (1996). Lung fibroblast alpha-smooth muscle actin expression and contractile phenotype in bleomycin-induced pulmonary fibrosis. Am J Pathol 148:527–37
  • Zhang K, Rekhter MD, Gordon D, Phan SH. (1994). Myofibroblasts and their role in lung collagen gene expression during pulmonary fibrosis. A combined immunohistochemical and in situ hybridization study. Am J Pathol 145:114–25

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.