2000
DOI: 10.1016/s0165-0378(99)00046-7
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MUC1/episialin: a critical barrier in the female reproductive tract

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Cited by 147 publications
(111 citation statements)
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“…MUC1 is a highly glycosylated transmembrane protein, expressed on mucosal surfaces of the stomach, lung, and amnion. Muc1 knockout mice have been found to have chronic uterine infection caused by overgrowth of normal bacteria of the reproductive tract (22). The structure and expression patterns of mucin proteins suggest that they may protect the mucous membranes by sterically inhibiting bacterial access to the cell membrane.…”
Section: Resultsmentioning
confidence: 99%
“…MUC1 is a highly glycosylated transmembrane protein, expressed on mucosal surfaces of the stomach, lung, and amnion. Muc1 knockout mice have been found to have chronic uterine infection caused by overgrowth of normal bacteria of the reproductive tract (22). The structure and expression patterns of mucin proteins suggest that they may protect the mucous membranes by sterically inhibiting bacterial access to the cell membrane.…”
Section: Resultsmentioning
confidence: 99%
“…The principal cysteine-rich, cationic, antimicrobial peptides expressed in the bovine endometrium include b-defensins, lingual antimicrobial peptide (LAP), and tracheal antimicrobial peptide (TAP), and their transcripts are more abundant in the face of microbial challenge (Davies et al 2008, Chapwanya et al 2013. Other surface molecules that may help to protect the endometrium include the mucins; evidence for their role includes genetic deletion of Muc1 in mice, which is associated with chronic inflammation of the lower female reproductive tract by opportunistic bacterial infections (DeSouza et al 1999). The expression of mRNA encoding acute-phase proteins in the uterus and ovary is also of interest, because they may provide further localised protection , Lecchi et al 2012, Chapwanya et al 2013).…”
Section: Innate Immunitymentioning
confidence: 99%
“…The expression of multiple cell-surface mucins with similar functional roles may explain why Muc1 null mice show no obvious signs of epithelial pathology (29), although these mice are also yet to be tested comprehensively with epithelial challenges. Interestingly, when Muc1 null mice were removed from a pathogen-free environment, they developed ocular and reproductive tract bacterial infections, implicating cell surface mucins in protection from epithelial bacterial infections (30,31).…”
Section: Fig 10 Glycosylation Of Muc13mentioning
confidence: 99%