4.7 Article

JAM-A regulates epithelial proliferation through Akt/β-catenin signalling

Journal

EMBO REPORTS
Volume 12, Issue 4, Pages 314-320

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/embor.2011.16

Keywords

junctional adhesion molecule; Akt; beta-catenin; cell proliferation; tight junction

Funding

  1. National Institutes of Health [DK72564, DK61379, DK79392, DK53202, DK55679, DK59888, DK64399]
  2. Crohn's and Colitis Foundation of America
  3. American Gastroenterological Association
  4. Division Of Integrative Organismal Systems
  5. Direct For Biological Sciences [0923827] Funding Source: National Science Foundation
  6. Crohn's & Colitis Foundation of America [2634] Funding Source: researchfish

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Expression of the tight junction protein junctional adhesion molecule-A (JAM-A) has been linked to proliferation and tumour progression. However, a direct role for JAM-A in regulating proliferative processes has not been shown. By using complementary in vivo and in vitro approaches, we demonstrate that JAM-A restricts intestinal epithelial cell (IEC) proliferation in a dimerization-dependent manner, by inhibiting Akt-dependent beta-catenin activation. Furthermore, IECs from transgenic JAM-A(-/-)/beta-catenin/T-cell factor reporter mice showed enhanced beta-catenin-dependent transcription. Finally, inhibition of Akt reversed colonic crypt hyperproliferation in JAM-A-deficient mice. These data establish a new link between JAM-A and IEC homeostasis.

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