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Comparison of the Transmembrane Mucins MUC1 and MUC16 in Epithelial Barrier Function
Author(s) -
Ilene K. Gipson,
Sandra Spurr-Michaud,
Ann Tisdale,
Balaraj B. Me
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0100393
Subject(s) - mucin , barrier function , muc1 , epithelium , microbiology and biotechnology , tight junction , apical membrane , transmembrane protein , mucin 2 , glycocalyx , intestinal epithelium , biology , gene knockdown , chemistry , cell culture , biochemistry , receptor , gene expression , gene , genetics
Membrane-anchored mucins are present in the apical surface glycocalyx of mucosal epithelial cells, each mucosal epithelium having at least two of the mucins. The mucins have been ascribed barrier functions, but direct comparisons of their functions within the same epithelium have not been done. In an epithelial cell line that expresses the membrane-anchored mucins, MUC1 and MUC16, the mucins were independently and stably knocked down using shRNA. Barrier functions tested included dye penetrance, bacterial adherence and invasion, transepithelial resistance, tight junction formation, and apical surface size. Knockdown of MUC16 decreased all barrier functions tested, causing increased dye penetrance and bacterial invasion, decreased transepithelial resistance, surprisingly, disruption of tight junctions, and greater apical surface cell area. Knockdown of MUC1 did not decrease barrier function, in fact, barrier to dye penetrance and bacterial invasion increased significantly. These data suggest that barrier functions of membrane-anchored mucins vary in the context of other membrane mucins, and MUC16 provides a major barrier when present.

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