Sialomucin complex at the rat ocular surface: a new model for ocular surface protection

被引:60
作者
Price-Schiavi, A
Meller, D
Jing, X
Merritt, J
Carvajal, ME
Tseng, SCG
Carraway, KL [1 ]
机构
[1] Univ Miami, Sch Med, Dept Cell Biol & Anat, Miami, FL 33101 USA
[2] Univ Miami, Sch Med, Dept Ophthalmol, Miami, FL 33101 USA
关键词
D O I
10.1042/bj3350457
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ocular surface, which is among the most accessible and vulnerable tissues in mammals, is protected by a complex tear film composed of lipid, aqueous and mucin layers. In spite of its importance, the molecular nature of the mucin contribution remains uncertain. Since membrane mucins have been implicated in the protection of other epithelia, we have analysed rat corneal and conjunctival tissues for sialomucin complex (SMC), a membrane mucin found at the apical epithelial cell surfaces in the airway and uterus. Using Northern and Western blot analyses, SMC expression was found in both ocular tissues, being particularly abundant in the cornea. In contrast with the other known membrane mucin, MUC1, SMC was localized more heavily towards the apical surface of the epithelial cells. SMC in ocular surface epithelia was produced in both soluble and membrane forms, the latter being found predominantly in the most superficial cells and at apical surfaces. The soluble form was found loosely adsorbed to apical cell surfaces, particularly of the cornea, as indicated by a mild rinsing protocol. Finally, the tear fluid contained substantial amounts of SMC. From these results, we propose a new model for tear mucin components in which SMC is expressed at the apical ocular surface in both membrane-bound and adsorbed soluble forms to provide a direct protective barrier. SMC secreted into the tear fluid may also participate in maintaining the stability of the preocular tear film by acting with other secreted mucins to determine the physical properties and protective behaviour of the tear film.
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页码:457 / 463
页数:7
相关论文
共 43 条
[1]  
BOBEK LA, 1993, J BIOL CHEM, V268, P20563
[2]  
BOLIS S, 1995, INVEST OPHTH VIS SCI, V36, pS421
[3]   THE PRODUCT OF THE HUMAN MUC1 GENE WHEN SECRETED BY MOUSE CELLS TRANSFECTED WITH THE FULL-LENGTH CDNA LACKS THE CYTOPLASMIC TAIL [J].
BOSHELL, M ;
LALANI, EN ;
PEMBERTON, L ;
BURCHELL, J ;
GENDLER, S ;
TAYLORPAPADIMITRIOU, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 185 (01) :1-8
[4]  
CARLSTEDT I, 1985, ESSAYS BIOCHEM, V20, P40
[5]   Roles of ErbB-3 and ErbB-4 in the Physiology and Pathology of the Mammary Gland [J].
Carraway, Kermit L. ;
Carraway, Coralie A. Carothers ;
Carraway, Kermit L., III .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 1997, 2 (02) :187-198
[6]   EFFECTS OF CYTOSKELETAL PERTURBANT DRUGS ON ECTO 5'-NUCLEOTIDASE, A CONCANAVALIN-A RECEPTOR [J].
CARRAWAY, KL ;
DOSS, RC ;
HUGGINS, JW ;
CHESNUT, RW ;
CARRAWAY, CAC .
JOURNAL OF CELL BIOLOGY, 1979, 83 (03) :529-543
[7]  
Chen HB, 1997, INVEST OPHTH VIS SCI, V38, P381
[8]   Ocular mucins: Purification, metabolism and functions [J].
Corfield, AP ;
Carrington, SD ;
Hicks, SJ ;
Berry, M ;
Ellingham, R .
PROGRESS IN RETINAL AND EYE RESEARCH, 1997, 16 (04) :627-656
[10]  
DILLY PN, 1985, T OPHTHAL SOC UK, V104, P381