DOI QR코드

DOI QR Code

Synovial Fluid Enhances Proliferation and Migration in Canine Keratocytes

  • Lee, Seungji (Department of Veterinary Surgery, College of Veterinary Medicine, Kyungpook National University) ;
  • Jeong, Seong Mok (Department of Veterinary Surgery, College of Veterinary Medicine, Chungnam National University) ;
  • Bae, Seul-gi (Department of Veterinary Internal Medicine, College of Veterinary Medicine, Kyungpook National University) ;
  • Kwon, Young-sam (Department of Veterinary Surgery, College of Veterinary Medicine, Kyungpook National University) ;
  • Yun, Sungho (Department of Veterinary Surgery, College of Veterinary Medicine, Kyungpook National University)
  • Received : 2020.05.26
  • Accepted : 2020.08.18
  • Published : 2020.08.31

Abstract

Synovial fluid (SF) contains various factors which may be helpful for corneal stromal healing, such as cytokines, growth factors, hyaluronic acid, and proteins. Therefore, the purpose of this study was to determine the effect of SF on proliferation and migration in canine keratocytes. In order to evaluate the degree of proliferation and migration, canine keratocytes were cultured in DMEM containing 1%, 3%, 5%, or 10% SF. Real-time PCR was performed in a control group and the group treated with 5% SF, in order to measure the expression levels of factors associated with corneal wound healing. These factors included interleukin-1α (IL-1α), hepatocyte growth factor (HGF), transforming growth factor-β (TGF-β), and α-smooth muscle actin (SMA-α). Proliferation assays demonstrated that proliferation was significantly enhanced in groups treated with greater than 3% SF, as compared with that of the control group. In addition, migration in all SF-treated groups was significantly increased as compared with migration in the control group, as measured by migration assays. mRNA expression of IL-1α and HGF was significantly increased and mRNA expression of TGF-β and SMA-α was significantly decreased in the cells treated with 5% SF. These findings suggest that SF may promote corneal wound healing.

Keywords

References

  1. Ahmadi AJ, Jakobiec FA. Corneal wound healing: cytokines and extracellular matrix proteins. Int Ophthalmol Clin 2002; 42: 13-22.
  2. Balazs EA. The physical properties of synovial fluid and the special role of hyaluronic acid. Disorders of the Knee 1974; 2: 61-74.
  3. Blewis ME, Nugent-Derfus GE, Schmidt TA, Schumacher BL, Sah RL. A model of synovial fluid lubricant composition in normal and injured joints. Eur Cell Mater 2007; 13: 26-39.
  4. Fredj-Reygrobellet D, Plouet J, Delayre T, Baudouin C, Bourret F, Lapalus P. Effects of aFGF and bFGF on wound healing in rabbit corneas. Curr Eye Res 1987; 6: 1205-1209.
  5. Fuchs TF, Petersen W, Vordemvenne T, Stange R, Raschke M, Paletta JR. Influence of synovial fluid on human osteoblasts: an in vitro study. Sci World J 2007; 18: 2012-2020.
  6. Gallego-Munoz P, Ibares-Frias L, Valsero-Blanco MC, Cantalapiedra-Rodriguez R, Merayo-Lloves J, Martinez-Garcia MC. Effects of $TGF{\beta}1$, PDGF-BB, and bFGF, on human corneal fibroblasts proliferation and differentiation during stromal repair. Cytokine 2017; 96: 94-101. https://doi.org/10.1016/j.cyto.2017.03.011
  7. Gobezie R, Kho A, Krastins B, Sarracino DA, Thornhill TS, Chase M, Millett PJ, Lee DM. High abundance synovial fluid proteome: distinct profiles in health and osteoarthritis. Arthritis Res Ther 2007; 9: R36.
  8. Gomes JA, Amankwah R, Powell-Richards A, Dua HS. Sodium hyaluronate(hyaluronic acid) promotes migration of human corneal epithelial cells in vitro. Br J Ophthalmol 2004; 88: 821-825. https://doi.org/10.1136/bjo.2003.027573
  9. Hamerman D, Taylor S, Kirschenbaum I, Klagsbrun M, Raines EW, Ross R, Thomas KA. Growth factors with heparin binding affinity in human synovial fluid. Proc Soc Exp Biol Med 1987; 186: 384-389.
  10. Hinz B. Myofibroblasts. Exp Eye Res 2016; 142: 56-70.
  11. Imanishi J, Kamiyama K, Iguchi I, Kita M, Sotozono C, Kinoshita S. Growth factors: importance in wound healing and maintenance of transparency of the cornea. Prog Retin Eye Res 2000; 19: 113-129.
  12. Jester JV, Ho-Chang J. Modulation of cultured corneal keratocyte phenotype by growth factors/cytokines control in vitro contractility and extracellular matrix contraction. Exp Eye Res 2003; 77: 581-592.
  13. Lambiase A, Manni L, Bonini S, Rama P, Micera A, Aloe L. Nerve growth factor promotes corneal healing: structural, biochemical, and molecular analyses of rat and human corneas. Invest Ophthalmol Vis Sci 2000; 41: 1063-1069.
  14. Lee DA, Salih V, Stockton EF, Stanton JS, Bentley G. Effect of normal synovial fluid on the metabolism of articular chondrocytes in vitro. Clin Orthop Relat Res 1997; 342: 228-238.
  15. Lettesjo H, Nordstrom E, Strom H, Nilsson B, Glinghammar B, Dahlstedt L, Moller E. Synovial fluid cytokines in patients with rheumatoid arthritis or other arthritic lesions. Scand J Immunol 1998; 48: 286-292. https://doi.org/10.1046/j.1365-3083.1998.00399.x
  16. Lim M, Goldstein MH, Tuli S, Schultz GS. Growth factor, cytokine and protease interactions during corneal wound healing. Ocul Surf 2003; 1: 53-65. https://doi.org/10.1016/S1542-0124(12)70128-3
  17. Ljubimov AV, Saghizadeh M. Progress in corneal wound healing. Prog Retin Eye Res 2015; 49: 17-45.
  18. Miyagi H, Thomasy SM, Russell P, Murphy CJ. The role of hepatocyte growth factor in corneal wound healing. Exp Eye Res 2018; 166: 49-55.
  19. Schalkwijk J, Joosten LA, van den Berg WB, van Wyk JJ, van de Putte LB. Insulin-like growth factor stimulation of chondrocyte proteoglycan synthesis by human synovial fluid. Arthritis Rheum 1989; 32: 66-71.
  20. Singh V, Barbosa FL, Torricelli AA, Santhiago MR, Wilson SE. Transforming growth factor ${\beta}$ and platelet-derived growth factor modulation of myofibroblast development from corneal fibroblasts in vitro. Exp Eye Res 2014; 120: 152-160.
  21. Sivak JM, Fini ME. MMPs in the eye: emerging roles for matrix metalloproteinases in ocular physiology. Prog Retin Eye Res 2002; 21: 1-14.
  22. Tandon A, Tovey JC, Sharma A, Gupta R, Mohan RR. Role of transforming growth factor Beta in corneal function, biology and pathology. Curr Mol Med 2010; 10: 565-578. https://doi.org/10.2174/1566524011009060565
  23. Werner A, Braun M, Kietzmann M. Isolation and cultivation of canine corneal cells for in vitro studies on the antiinflammatory effects of dexamethasone. Vet Ophthalmol 2008; 11: 67-74. https://doi.org/10.1111/j.1463-5224.2008.00602.x
  24. West-Mays JA, Sadow PM, Tobin TW, Strissel KJ, Cintron C, Fini ME. Repair phenotype in corneal fibroblasts is controlled by an interleukin-1 alpha autocrine feedback loop. Invest Ophthalmol Vis Sci 1997; 38: 1367-1379.
  25. Wilson SE. Corneal myofibroblast biology and pathobiology: generation, persistence, and transparency. Exp Eye Res 2012; 99: 78-88.
  26. Wilson SE, Mohan RR, Ambrosio R Jr, Hong J, Lee J. The corneal wound healing response: cytokine-mediated interaction of the epithelium, stroma, and inflammatory cells. Prog Retin Eye Res 2001; 20: 625-637.
  27. Yang KG, Saris DB, Verbout AJ, Creemers LB, Dhert WJ. The effect of synovial fluid from injured knee joints on in vitro chondrogenesis. Tissue Eng 2006; 12: 2957-2964. https://doi.org/10.1089/ten.2006.12.2957