| First Author | Parmley RR | Year | 1998 |
| Journal | J Clin Invest | Volume | 102 |
| Issue | 10 | Pages | 1798-806 |
| PubMed ID | 9819365 | Mgi Jnum | J:51108 |
| Mgi Id | MGI:1314597 | Doi | 10.1172/JCI3820 |
| Citation | Parmley RR, et al. (1998) Cystic fibrosis mice lacking Muc1 have reduced amounts of intestinal mucus. J Clin Invest 102(10):1798-806 |
| abstractText | Normally a thin layer of mucus covers the surface of the gastrointestinal tract protecting the epithelial cells from their environment. In cystic fibrosis (CF), mucus accumulation is abnormally high, resulting in severe intestinal obstruction. The major structural components of mucus are large mucin glycoproteins. We determined specific mucin RNA and protein expression in the gastrointestinal tract of inbred CF transmembrane conductance regulator (CFTR) knockout (CF) mice and correlated expression with histological analyses of tissues. Mucins were detected histochemically using general carbohydrate stains and specific mucin antibodies. Mucin RNA levels were determined by reverse transcription-PCR. Comparisons were made between CF mice and control siblings, all maintained on a liquid diet after weaning. Analyses of the mucins Muc2, Muc3, and Muc5ac showed lower levels of RNA expression in the CF mice and similar levels of protein. Significantly, there was a sixfold increase in Muc1 RNA expression in the colon of the CF mouse and a moderate increase in Muc1 protein. Further, CF mice lacking Muc1 exhibited greatly diminished intestinal mucus obstruction when compared with Muc1- expressing CF mice and had better survival on solid food. We suggest that Muc1 plays an important role in the mucus obstructions observed in the gastrointestinal tract of the CFTR knockout mouse. |
