Functions of MUC16 in corneal epithelial cells

被引:162
作者
Blalock, Timothy D.
Spurr-Michaud, Sandra J.
Tisdale, Ann S.
Heimer, Susan R.
Gilmore, Michael S.
Ramesh, Vijaya
Gipson, Ilene K.
机构
[1] Harvard Univ, Sch Med, Schepens Eye Res Inst, Dept Ophthalmol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Mol Neurogenet Unit, Charlestown, MA USA
关键词
D O I
10.1167/iovs.07-0430
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. The membrane-associated mucin MUC16, a heavily O-glycosylated transmembrane protein, is expressed by the ocular surface epithelia and localized on the tips of the surface microplicae. Although its functions in the ocular surface glycocalyx are unknown, it is thought that MUC16 provides a disadhesive barrier to the epithelial membrane. Two other membrane-associated mucins expressed by ocular surface epithelia, MUC1 and MUC4, are multifunctional and have signaling capabilities through their cytoplasmic tails and EGF-like domains, respectively. The MUC16 cytoplasmic tail has not been characterized, but, because it contains a polybasic amino acid sequence, it potentially interacts with the actin cytoskeleton through ezrin/radixin/moesin (ERM) actin-binding proteins. METHODS. The interaction of MUC16 with the actin cytoskeleton through ERMs was investigated using cytoplasmic tail peptides and ERM pull-down experiments. MUC16 functions were determined using RNA interference in immortalized human corneal-limbal epithelial (HCLE) cells. The effect of MUC16 knockdown on microplicae structure in HCLE cells was determined using scanning and immunoelectron microscopy. HCLE cells were incubated with rose bengal dye to measure the role of MUC16 in ocular surface barrier function. Binding of fluorescently labeled Staphylococcus aureus to HCLE cells was measured to determine the role of MUC16 in the protection of pathogen adherence on the ocular surface epithelium. RESULTS. MUC16 cytoplasmic tail peptides bound the N-terminus of ERMs, with no detectable binding of MUC1 and MUC4 peptides. No effect on surface membrane projections could be detected in HCLE cells after MUC16 suppression; however, HCLE cells incubated with rose bengal showed that exclusion of the dye was significantly reduced in cells with MUC16 suppression. In addition, S. aureus binding to HCLE cells was significantly increased with MUC16 suppression. CONCLUSIONS. These results suggest that MUC16 is a multifunctional molecule linked to the actin cytoskeleton. The expression of MUC16 in the ocular surface glycocalyx helps provide a disadhesive protective barrier for the epithelial surface.
引用
收藏
页码:4509 / 4518
页数:10
相关论文
共 55 条
[1]  
Abramoff MD., 2004, Biophot. Int., V11, P36
[2]   SUBCELLULAR-LOCALIZATION OF MOESIN IN DYNAMIC FILOPODIA, RETRACTION FIBERS, AND OTHER STRUCTURES INVOLVED IN SUBSTRATE EXPLORATION, ATTACHMENT, AND CELL-CELL CONTACTS [J].
AMIEVA, MR ;
FURTHMAYR, H .
EXPERIMENTAL CELL RESEARCH, 1995, 219 (01) :180-196
[3]   MUC16 mucin is expressed by the human ocular surface epithelia and carries the H185 carbohydrate epitope [J].
Argüeso, P ;
Spurr-Michaud, S ;
Russo, CL ;
Tisdale, A ;
Gipson, IK .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (06) :2487-2495
[4]   Mucin characteristics of human corneal-limbal epithelial cells that exclude the rose bengal anionic dye [J].
Argüeso, P ;
Tisdale, A ;
Spur-Michaud, S ;
Sumiyoshi, M ;
Gipson, IK .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (01) :113-119
[5]   Characterization of a carbohydrate epitope defined by the monoclonal antibody H185:: sialic acid O-acetylation on epithelial cell-surface mucins [J].
Argueso, Pablo ;
Sumiyoshi, Mika .
GLYCOBIOLOGY, 2006, 16 (12) :1219-1228
[6]   MEMBRANE-ACTIN MICROFILAMENT CONNECTIONS - AN INCREASING DIVERSITY OF PLAYERS RELATED TO BAND-4.1 [J].
ARPIN, M ;
ALGRAIN, M ;
LOUVARD, D .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (01) :136-141
[7]  
Bretscher A, 1997, J CELL SCI, V110, P3011
[8]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[9]  
Danjo Y, 1998, INVEST OPHTH VIS SCI, V39, P2602
[10]  
DeSouza MM, 1999, J REPROD IMMUNOL, V45, P127, DOI 10.1016/S0165-0378(99)00046-7