Expression of MUC2 and MUC3 mRNA in human normal, malignant, and inflammatory intestinal tissues.

AA Weiss, MW Babyatsky, S Ogata… - … of Histochemistry & …, 1996 - journals.sagepub.com
AA Weiss, MW Babyatsky, S Ogata, A Chen, SH Itzkowitz
Journal of Histochemistry & Cytochemistry, 1996journals.sagepub.com
MUC2 and MUC3 are prominent mucin genes expressed in the human intestine. Using in
situ hybridization with RNA probes, we examined the cellular distribution of MUC2 and
MUC3 mRNA in normal, malignant, and inflammatory human intestinal tissues. In normal
small intestine and colon, MUC2 mRNA was expressed exclusively in goblet cells and
occurred throughout the entire height of the mucosa. MUC3 mRNA was expressed by goblet
and columnar cells but was restricted to the villous compartment of the small intestine and …
MUC2 and MUC3 are prominent mucin genes expressed in the human intestine. Using in situ hybridization with RNA probes, we examined the cellular distribution of MUC2 and MUC3 mRNA in normal, malignant, and inflammatory human intestinal tissues. In normal small intestine and colon, MUC2 mRNA was expressed exclusively in goblet cells and occurred throughout the entire height of the mucosa. MUC3 mRNA was expressed by goblet and columnar cells but was restricted to the villous compartment of the small intestine and the surface epithelium of the colon. Expression of MUC2 and MUC3 mRNA were both markedly decreased in poorly, moderately, and well-differentiated colon cancers but were preserved in mucinous colon cancers. In ulcerative colitis and Crohn's colitis tissues, MUC2 and MUC3 mRNA expression displayed a normal pattern regardless of whether the mucosa manifested active or quiescent inflammation. These findings indicate that MUC2 is goblet cell-specific, whereas MUC3 is related to maturation of intestinal epithelial cells. In colon cancers, the genetic regulation of MUC2 and MUC3 is different depending on the histological type of tumor. The constitutive expression of MUC2 and MUC3 mRNA in inflammatory bowel diseases suggests that these genes may be necessary for maintenance of normal epithelial cell function during inflammation.
Sage Journals