Expression and distribution of adhesion molecule CD44 in healing corneal epithelia

Investigative Ophthalmology and Visual Science

Volumn 39, Issue 5, 1998, Pages 710-717

  Yu, Fushin X ^a   Guo, Jing ^a   Zhang, Qiang ^a  

^a SCHEPENS EYE RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HERMES ANTIGEN; MESSENGER RNA;

ANIMAL TISSUE; ANTIGEN EXPRESSION; ARTICLE; CELL ADHESION; CELL INTERACTION; CELL MIGRATION; CONTROLLED STUDY; CORNEA EPITHELIUM; CORNEA INJURY; EPITHELIZATION; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; NONHUMAN; PRIORITY JOURNAL; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; WOUND HEALING;

ALTERNATIVE SPLICING; ANIMALS; ANTIGENS, CD44; CELL ADHESION; DNA PRIMERS; EPITHELIUM, CORNEAL; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; IN SITU HYBRIDIZATION; POLYMERASE CHAIN REACTION; RATS; RATS, SPRAGUE-DAWLEY; RNA; RNA, MESSENGER; WOUND HEALING;

EID: 0031957971     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (46)

1. Dua H, Gomes J, Singh A. Corneal epitheila wound healing. Br J Ophthalmol. 1994;78:401-408.
2. Woodley D, Reepithelialization. In: Clark R, ed. The Molecular and Cellular Biology of Wound Repair. New York: Plenum Press; 1996:339-350.
3. Clark, R. Wound repair: overview and general consideration. In: Clark R, ed. The Molecular and Cellular Biology of Wound Repair, New York: Plenum Press; 1996:3-50.
4. Gipson I, Sugrue S. Cell biology of the corneal epithelium. In: Albert D, Jakobiec F, eds. Principles and Practice of Ophthalmology. Philadelphia: WB Saunders, 1994:3-16.
5. Faassen AE, Schrager JA, Klein DJ, Oegema TR, Couchman JR, McCarthy JB. A cell surface chondroitin sulfate proteoglycan, immunologically related to CD44, is involved in type I collagenmediated melanoma cell motility and invasion. J Cell Biol. 1992; 116:521-531.
6. Lesley J, Hyman R, Kincade PW. CD44 and its interaction with extracellular matrix. Adv Immunol. 1993;54:271-335.
7. Naor D, Sionov R, and Ish-Shalon D. CD44: Structure, function, and association with the malignant process. Adv Cancer Res. 1997;71:241-319.
8. Stamenkovic I, Amiot M, Pesando J, Seed B. A lymphocyte molecule implicated in lymph node homing is a member of the cartilage link protein family. Cell. 1989;56:1057-1062.
9. Goldstein L, Zhou D, Picker L, et al. A human lymphocyte homing receptor, the hermes antigen, is related to cartilage proteoglycan core and link proteins. Cell. 1989;56:1063-1072.
10. Screaton G, Bell M, Bell J, Jackson D. The identification of a new alternative exon with highly restricted tissue expression in transcripts encoding the mouse Pgp-1 (CD44) homing receptor. Comparison of all 10 variable exons between mouse, human, and rat. J Biol Chem. 1993;268:12235-12238.
11. Screaton G, Bell M, Jackson D, Cornelis F, Gerth U, Bell J. Genomic structure of DNA encoding the lymphocyte homing receptor CD44 reveals at least 12 alternatively spliced exons. Proc Natl Acad Sci USA. 1992;89:12160-12164.
12. Gunthert U. CD44: a multitude of isoforms with diverse functions. Curr Top Microbiol Immunol. 1993;184:47-63.
13. Aruffo A, Stamenkovic I, Melnick M, Underhill CB, Seed B. CD44 is the principal cell surface receptor for hyaluronate. Cell. 1990;61: 1303-1313.
14. Jalkanen S, Jalkanen M. Lymphocyte CD44 binds the COOH-terminal heparin-binding domain of fibronectin. J Cell Biol. 1992;116: 817-825.
15. Verfaillie CM, Benis A, Iida J, McGlave PB, McCarthy JB. Adhesion of committed human hematopoietic progenitors to synthetic peptides from the C-terminal heparin-binding domain of fibronectin: cooperation between the integrin alpha 4 beta 1 and the CD44 adhesion receptor. Blood. 1994;84:1802-1811.
16. Knutson JR, Iida J, Fields GB, McCarthy JB. CD44/chondroitin sulfate proteoglycan and alpha 2 beta 1 integrin mediate human melanoma cell migration on type IV collagen and invasion of basement membranes. Mol Biol Cell. 1996;7:383-396.
17. Ehnis T, Dieterich W, Bauer M, Lampe B, Schuppan D. A chondroitin/dermatan sulfate form of CD44 is a receptor for collagen XIV (undulin). Exp Cell Res. 1996;229:388-397.
18. Naujokas M, Morin M, Anderson M, Peterson M, Miller J. The chondroitin sulfate form of invariant chain can enhance stimulation of T cell responses through interaction with CD44. Cell. 1993;74:257-268.
19. Toyama SN, Sorimachi H, Tobita Y, Kitamura F, Yagita H, Suzuki K, Miyasaka M. A novel ligand for CD44 is serglycin, a hematopoietic cell lineage-specific proteoglycan. Possible involvement in lymphoid cell adherence and activation. J Biol Chem. 1995;270:7437-7444.
20. Spurr MSJ, Barza M, Gipson IK. An organ culture system for study of adherence of Pseudomonas aeruginosa to normal and wounded corneas. Invest Ophthalmol Vis Sci. 1988;29:379-386.
21. Yu FX, Gipson IK, Guo Y. Differential gene expression in healing rat corneal epithelium. Invest Ophthalmol Vis Sci. 1995;36:1997-2007.
22. Arch R, Wirth K, Hofmann M, et al. Participation in normal immune responses of a metastasis-inducing splice variant of CD44. Science. 1992;257:682-685.
23. He QJL, Hyman R, Ishihara K, Kincade P. Molecular isoforms of murine CD44 and evidence that the membrane proximal domain is not critical for hyaluronate recognition. J Cell Biol. 1992;119: 1711-1719.
24. Gunthert U, Hofmann M, Rudy W, et al. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell. 1991;65:13-24.
25. Huang A, Li C, Che Y, Bourguignon, L. Co-expression of bcl-2 and CD44s in basal layers of human ocular surface epithelia. In: Sullivan D, Dartt D, Meneray M, Eds. Advances in Experimental Medicine and Biology. New York: Plenum Press; in press.
26. Bennett KL, Modrell B, Greenfield B, et al. Regulation of CD44 binding to hyaluronan by glycosylation of variably spliced exons. J Cell Biol. 1995;131:1623-1633.
27. Bennett KL, Jackson DG, Simon, et al. CD44 isoforms containing exon V3 are responsible for the presentation of heparin-binding growth factor. J Cell Biol. 1995;128:687-698.
28. Kuwabara T, Perkins D, Cogan D. Sliding of the epithelium in experimental corneal wounds. Invest Ophthalmol. 1976;15:4-14.
29. Pei Y, Rhodin J. Electron microscopic study of the development of the mouse corneal epithelium. Invest Ophthalmol. 1971;10:811-825.
30. Hogan M, Alvardo J, Weddell J. Histology of the Human Eye. Philadelphia: WB Saunders; 1971.
31. McLaughlin B, Caldwell R, Sasaki Y, Wood T. Freeze-fracture quantitative comparison of rabbit corneal epithelial and endothelial membranes. Curr Eye Res. 1985;4:951-961.
32. Sugrue S, Zieske J. ZO1 in corneal epithelium: association to the zonula occludens and adherens junctions. Exp Eye Res. 1997;64: 11-20.
33. Mackay D, Esch F, Furthmayr H, Hall A. Rho-and rac-dependent assembly of focal adhesion complexes and actin filaments in permeabilized fibroblasts: an essential role for ezrin/radixin/moesin proteins. J Cell Biol. 1997;138:927-938.
34. Sugrue S. Regulation of cell adhesion in the corneal epithelium [ARVO Abstract]. Invest Ophthalmol Vis Res. 1997;38:S923.
35. Milstone LM, Hough ML, Kugelman LC, Bender JR, Haggerty JG. Epican, a heparan/chondroitin sulfate proteoglycan form of CD44, mediates cell-cell adhesion. J Cell Sci. 1994;107:3183-3190.
36. Gipson IK, Spurr MS, Tisdale A, Elwell J, Stepp MA. Redistribution of the hemidesmosome components alpha 6 beta 4 integrin and bullous pemphigoid antigens during epithelial wound healing. Exp Cell Res. 1993;207:86-98.
37. Stepp MA, Spurr MS, Gipson IK. Integrins in the wounded and unwounded stratified squamous epithelium of the cornea. Invest Ophthalmol Vis Sci. 1993;34:1829-1844.
38. Stock EL, Kurpakus MA, Sambol B, Jones JC. Adhesion complex formation after small keratectomy wounds in the cornea. Invest Ophthalmol Vis Sci. 1992;33:304-313.
39. Grushkin LL, Trinkaus RV. Localization of integrin and syndecan in vivo in a corneal epithelial abrasion and keratectomy. Curr Eye Res. 1991;10:75-85.
40. Faassen AE, Mooradian DL, Tranquillo RT, et al. Cell surface CD44-related chondroitin sulfate proteoglycan is required for transforming growth factor-beta-stimulated mouse melanoma cell motility and invasive behavior on type I collagen. J Cell Sci. 1993;105:501-511.
41. Clark R, Alon R, Springer T. CD44 and hyaluronan-dependent rolling interactions of lymphocytes on tonsillar stroma. J Cell Biol. 1996;134:1075-1087.
42. Okada H, Yoshida J, Sokabe M, Wakabayashi T, Hagiwara M. Suppression of CD44 expression decreases migration and invasion of human glioma cells. Int J Cancer. 1996;66:255-260.
43. Svee K, White J, Vaillant P, et al. Acute lung injury fibroblast migration and invasion of a fibrin matrix is mediated by CD44. J Clin Invest. 1996;98:1713-1727.
44. Rosel M, Seiter S, Zoller M. CD44v10 expression in the mouse and functional activity in delayed type hypersensitivity. J Cell Physiol. 1997;171:305-317.
45. Ramirez A, Bravo A, Jorcano JL, Vidai M. Sequences 5′ of the bovine keratin 5 gene direct tissue-and cell-type-specific expression of a lacZ gene in the adult and during development. Differentiation. 1994;58:53-64.
46. Kaya G, Rodriguez I, Jorcano JL, Vassalli P, Stamenkovic I. Selective suppression of CD44 in keratinocytes of mice bearing an antisense CD44 transgene driven by a tissue-specific promoter disrupts hyaluronate metabolism in the skin and impairs keratinocyte proliferation. Genes Dev. 1997;11:996-1007.