Arhgap17, a RhoGTPase activating protein, regulates mucosal and epithelial barrier function in the mouse colon

So Young Lee, Hwain Kim, Kyoungmi Kim, Hyunji Lee, Seungbok Lee, Daekee Lee

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


Coordinated regulation of the actin cytoskeleton by the Rho GTPase family is required for the maintenance of polarity in epithelial cells as well as for their proliferation and migration. A RhoGTPase-activating protein 17 (Arhgap17) is known to be involved in multiple cellular processes in vitro, including the maintenance of tight junctions and vesicle trafficking. However, the function of Arhgap17 has not been studied in the physiological context. Here, we generated Arhgap17-deficient mice and examined the effect in the epithelial and mucosal barriers of the intestine. Reporter staining revealed that Arhgap17 expression is limited to the luminal epithelium of intestine. Arhgap17-deficient mice show an increased paracellular permeability and aberrant localization of the apical junction complex in the luminal epithelium, but do not develop spontaneous colitis. The inner mucus layer is impervious to the enteric bacteria irrespective of Tff3 downregulation in the Arhgap17-deficient mice. Interestingly however, treatment with dextran sulfate sodium (DSS) causes an increased accumulation of DSS and TNF production in intraluminal cells and rapid destruction of the inner mucus layer, resulting in increased severity of colitis in mutant mice. Overall, these data reveal that Arhgap17 has a novel function in regulating transcellular transport and maintaining integrity of intestinal barriers.

Original languageEnglish
Article number26923
JournalScientific Reports
StatePublished - 27 May 2016

Bibliographical note

Funding Information:
We thank Dr. Hansson at Uppsala University for providing the manual for staining the mucus layer and valuable comments on mucus staining and Dr. Nam, Kitak at Yeonsei University for providing the Tff3 antibody. We also thank Dr. Jaesang Kim at Ewha Womans University for critical reading of the manuscript. This work was supported by the National Research Foundation of Korea (2011K000281; 2012M3A9C5048707) from Korea Government. K. Kim was a beneficiary of Ewha Womans University Postdoctoral fellowship.


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