Hyaluronan Modulates Proliferation and Migration of Rabbit Fibroblasts Derived From Flexor Tendon Epitenon and Endotenon

Journal of Hand Surgery

Volumn 35, Issue 5, 2010, Pages 791-796

  Yagi, Masaharu ^a   Sato, Naoto ^a   Mitsui, Yasuhiro ^a   Gotoh, Masafumi ^a   Hamada, Tetsuya ^a   Nagata, Kensei ^a  

^a KURUME UNIVERSITY   (Japan)

Author keywords

CD44; cell migration; cell proliferation; flexor tendon; hyaluronan

Indexed keywords

HERMES ANTIGEN; HYALURONIC ACID;

ANIMAL CELL; ANIMAL TISSUE; ANTIGEN EXPRESSION; ARTICLE; CELL COUNT; CELL MIGRATION; CELL PROLIFERATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG EFFICACY; DRUG MECHANISM; FIBROBLAST; FLEXOR TENDON ENDOTENON; FLEXOR TENDON EPITENON; FLOW CYTOMETRY; GROWTH INHIBITION; MALE; MONOLAYER CULTURE; NONHUMAN; PRIORITY JOURNAL; RABBIT; TENDON; WOUND HEALING;

ANIMALS; ANTIGENS, CD44; CELL MOVEMENT; CELL PROLIFERATION; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; FIBROBLASTS; HINDLIMB; HYALURONIC ACID; MALE; RABBITS; TENDONS;

EID: 77951531609     PISSN: 03635023     EISSN: 15316564     Source Type: Journal    
DOI: 10.1016/j.jhsa.2010.02.010     Document Type: Article

References (41)

1. Potenza A.D. Prevention of adhesion to healing digital flexor tendons. JAMA 187 (1964) 187-191
2. Zhao C., Sun Y.L., Amadio P.C., Tanaka T., Ettema A.M., and An K.N. Surface treatment of flexor tendon autografts with carbodiimide-derivatized hyaluronic acid: an in vivo canine model. J Bone Joint Surg 88A (2006) 2181-2191
3. Kitsis C.K., Wade P.J., Krikler S.J., Parsons N.K., and Nicholls L.K. Controlled active motion following primary flexor tendon repair: a prospective study over 9 years. J Hand Surg 23B (1998) 344-349
4. Small J.O., Brennen M.D., and Colville J. Early active mobilisation following flexor tendon repair in zone 2. J Hand Surg 14B (1989) 383-391
5. Lister G.D., Kleinert H.E., Kutz J.E., and Atasoy E. Primary flexor tendon repair followed by immediate controlled mobilization. J Hand Surg 2 (1977) 441-451
6. Gelberman R.H., Boyer M.I., Brodt M.D., Winters S.C., and Silva M.J. The effect of gap formation at the repair site on the strength and excursion of intrasynovial flexor tendons: an experimental study on the early stages of tendon-healing in dogs. J Bone Joint Surg 81A (1999) 975-982
7. Zhao C., Amadio P.C., Tanaka T., Kutsumi K., Tsubone T., Zobitz M.E., et al. Effect of gap size on gliding resistance after flexor tendon repair. J Bone Joint Surg 86A (2004) 2482-2488
8. Golash A., Kay A., Warner J.G., Peck F., Watson J.S., and Lees V.C. Efficacy of ADCON-T/N after primary flexor tendon repair in Zone II: a controlled clinical trial. J Hand Surg 28B (2003) 113-115
9. Hanff G., and Hagberg L. Prevention of restrictive adhesions with expanded polytetrafluoroethylene diffusible membrane following flexor tendon repair: an experimental study in rabbits. J Hand Surg 23A (1998) 658-664
10. Cerovac S., Afoke A., Akali A., and McGrouther D.A. Early breaking strength of repaired flexor tendon treated with 5-fluorouracil. J Hand Surg 26B (2001) 220-223
11. Karakurum G., Buyukbebeci O., Kalender M., and Gulec A. Seprafilm interposition for preventing adhesion formation after tenolysis: an experimental study on the chicken flexor tendons. J Surg Res 113 (2003) 195-200
12. Chen W.Y., and Abatangelo G. Functions of hyaluronan in wound repair. Wound Repair Regen 7 (1999) 79-89
13. Wisniewski H.G., Hua J.C., Poppers D.M., Naime D., Vilcek J., and Cronstein B.N. TNF/IL-1-inducible protein TSG-6 potentiates plasmin inhibition by inter-alpha-inhibitor and exerts a strong anti-inflammatory effect in vivo. J Immunol 156 (1996) 1609-1615
14. Fraser J.R., Laurent T.C., and Laurent U.B. Hyaluronan: its nature, distribution, functions and turnover. J Intern Med 242 (1997) 27-33
15. Amiel D., Ishizue K., Billings Jr. E., Wiig M., Vande Berg J., Akeson W.H., et al. Hyaluronan in flexor tendon repair. J Hand Surg 14A (1989) 837-843
16. St Onge R., Weiss C., Denlinger J.L., and Balazs E.A. A preliminary assessment of Na-hyaluronate injection into "no man's land" for primary flexor tendon repair. Clin Orthop Relat Res 146 (1980) 269-275
17. Thomas S.C., Jones L.C., and Hungerford D.S. Hyaluronic acid and its effect on postoperative adhesions in the rabbit flexor tendon: a preliminary look. Clin Orthop Relat Res 206 (1986) 281-289
18. Hagberg L., and Gerdin B. Sodium hyaluronate as an adjunct in adhesion prevention after flexor tendon surgery in rabbits. J Hand Surg 17A (1992) 935-941
19. Tatari H., Skiak E., Destan H., Ulukuş C., Ozer E., and Satoǧlu S. Effect of hylan G-F 20 in Achilles' tendonitis: an experimental study in rats. Arch Phys Med Rehabil 85 (2004) 1470-1474
20. Yagishita K., Sekiya I., Sakaguchi Y., Shinomiya K., and Muneta T. The effect of hyaluronan on tendon healing in rabbits. Arthroscopy 21 (2005) 1330-1336
21. Salti N.I., Tuel R.J., and Mass D.P. Effect of hyaluronic acid on rabbit profundus flexor tendon healing in vitro. J Surg Res 55 (1993) 411-415
22. Hagberg L. Exogenous hyaluronate as an adjunct in the prevention of adhesions after flexor tendon surgery: a controlled clinical trial. J Hand Surg 17A (1992) 132-136
23. Wiig M., Abrahamsson S.O., and Lundborg G. Tendon repair: cellular activities in rabbit deep flexor tendons and surrounding synovial sheaths and the effects of hyaluronan: an experimental study in vivo and in vitro. J Hand Surg 22A (1997) 818-825
24. Meyers S.A., Seaber A.V., Glisson R.R., and Nunley J.A. Effect of hyaluronic acid/chondroitin sulfate on healing of full-thickness tendon lacerations in rabbits. J Orthop Res 7 (1989) 683-689
25. de Wit T., de Putter D., Tra W.M., Rakhorst H.A., van Osch G.J., Hovius S.E., et al. Auto-crosslinked hyaluronic acid gel accelerates healing of rabbit flexor tendons in vivo. J Orthop Res 27 (2009) 408-415
26. Underhill C. CD44: the hyaluronan receptor. J Cell Sci 103 (1992) 293-298
27. Gunthert U., Hofmann M., Rudy W., Reber S., Zoller M., Haussmann I., et al. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell 5; (1991) 65 :13-24
28. Jalkanen S., Bargatze R.F., de los Toyos J., and Butcher E.C. Lymphocyte recognition of high endothelium: antibodies to distinct epitopes of an 85-95-kD glycoprotein antigen differentially inhibit lymphocyte binding to lymph node, mucosal, or synovial endothelial cells. J Cell Biol 105 (1987) 983-990
29. Miyake K., Medina K.L., Hayashi S., Ono S., Hamaoka T., and Kincade P.W. Monoclonal antibodies to Pgp-1/CD44 block lympho-hemopoiesis in long-term bone marrow cultures. J Exp Med 171 (1990) 477-488
30. Shimizu Y., Van Seventer G.A., Siraganian R., Wahl L., and Shaw S. Dual role of the CD44 molecule in T cell adhesion and activation. J Immunol 143 (1989) 2457-2463
31. Yamada T., Gotoh M., Nakama K., Mitsui Y., Higuchi F., and Nagata K. Effects of hyaluronan on cell proliferation and mRNA expression of procollagens alpha 1 (I) and alpha 1 (III) in tendon-derived fibroblasts from patients with rotator cuff disease: an in vitro study. Am J Sports Med 35 (2007) 1870-1876
32. Nago M., Mitsui Y., Gotoh M., Nakama K., Shirachi I., Higuchi F., et al. Hyaluronan modulates cell proliferation and mRNA expression of adhesion-related procollagens and cytokines in glenohumeral synovial/capsular fibroblasts in adhesive capsulitis. J Orthop Res (Jan 7, 2010) Epub ahead of print. PMID: 20058278
33. Gelberman R.H., Amiel D., and Harwood F. Genetic expression for type I procollagen in the early stages of flexor tendon healing. J Hand Surg 17A (1992) 551-558
34. Russell J.E., and Manske P.R. Collagen synthesis during primate flexor tendon repair in vitro. J Orthop Res 8 (1990) 13-20
35. Abrahamsson S.O., Lundborg G., and Lohmander L.S. Restoration of the injured flexor tendon surface: a possible role for endotenon cells. A morphological study of the rabbit tendon in vivo. J Hand Surg 17B (1992) 553-560
36. Ishii S., and Umeda H. Role of tendon tissues in healing: a morphological study in vitro and in vivo. In: Hunter J.M. (Ed). Tendon surgery in the hand (1987), Mosby, St. Louis 79-85
37. Mitsui Y., Gotoh M., Nakama K., Yamada T., Higuchi F., and Nagata K. Hyaluronic acid inhibits mRNA expression of proinflammatory cytokines and cyclooxygenase-2/prostaglandin E(2) production via CD44 in interleukin-1-stimulated subacromial synovial fibroblasts from patients with rotator cuff disease. J Orthop Res 26 (2008) 1032-1037
38. Wiig M., Abrahamsson S.O., and Lundborg G. Effects of hyaluronan on cell proliferation and collagen synthesis: a study of rabbit flexor tendons in vitro. J Hand Surg 21A (1996) 599-604
39. Gomes J.A., Amankwah R., Powell-Richards A., and Dua H.S. Sodium hyaluronate (hyaluronic acid) promotes migration of human corneal epithelial cells in vitro. Br J Ophthalmol 88 (2004) 821-825
40. Maniwa S., Ochi M., Motomura T., Nishikori T., Chen J., and Naora H. Effects of hyaluronic acid and basic fibroblast growth factor on motility of chondrocytes and synovial cells in culture. Acta Orthop Scand 72 (2001) 299-303
41. Aruffo A., Stamenkovic I., Melnick M., Underhill C.B., and Seed B. CD44 is the principal cell surface receptor for hyaluronate. Cell 61 (1990) 1303-1313