In the current study we aimed to gain insight into epithelial-mesenchymal cross-talk and progenitor compartment modulation during doxorubicin (DOX)-induced mucositis in mice. Intestinal segments were collected on various days after DOX treatment. DOX-induced damage at day 1-2 was characterized by increased epithelial proliferation and apoptosis and a decrease in the expression of epithelial differentiation markers. Concurrently, T-cell factor-4 (TCF4) levels increased and the epithelial differentiation enhancing factor, bone morphogenic protein-4 (BMP4), decreased. During severe damage (day 3), BMP4 levels were significantly increased, which inversely correlated with epithelial proliferation. At the same time, the expression of the epithelial differentiation markers was increasing again. At day 7, BMP4 levels were down-regulated, while the levels of the epithelial differentiation markers and TCF4 were normalized again. These data suggest that in response to DOX-induced damage, BMP4 and TCF4 are modulated in such a way that homeostasis of the progenitor compartment is partly preserved.

, , , ,,
Digestive Diseases and Sciences
Erasmus MC: University Medical Center Rotterdam

de Koning, B., Lindenbergh-Kortleve, D., Pieters, R., Büller, H., Renes, I., & Einerhand, S. (2007). Alterations in epithelial and mesenchymal intestinal gene expression during doxorubicin-induced mucositis in mice. Digestive Diseases and Sciences, 52(8), 1814–1825. doi:10.1007/s10620-006-9174-5