Disruption of Rab8a and Rab11a causes formation of basolateral microvilli in neonatal enteropathy.

Feng Q, Bonder EM, Engevik AC, Zhang L, Tyska MJ, Goldenring JR, Gao N
J Cell Sci. 2017 130 (15): 2491-2505

PMID: 28596241 · PMCID: PMC5558269 · DOI:10.1242/jcs.201897

Misplaced formation of microvilli to basolateral domains and intracellular inclusions in enterocytes are pathognomonic features in congenital enteropathy associated with mutation of the apical plasma membrane receptor syntaxin 3 (STX3). Although the demonstrated binding of Myo5b to the Rab8a and Rab11a small GTPases implicates cytoskeleton-dependent membrane sorting, the mechanisms underlying the microvillar location defect remain unclear. By selective or combinatory disruption of Rab8a and Rab11a membrane traffic , we demonstrate that transport of distinct cargo to the apical brush border rely on either individual or both Rab regulators, whereas certain basolateral cargos are redundantly transported by both factors. Enterocyte-specific and double-knockout mouse neonates showed immediate postnatal lethality and more severe enteropathy than single knockouts, with extensive formation of microvilli along basolateral surfaces. Notably, following an inducible deletion from neonatal enterocytes, basolateral microvilli were induced within 3 days. These data identify a potentially important and distinct mechanism for a characteristic microvillus defect exhibited by enterocytes of patients with neonatal enteropathy.

© 2017. Published by The Company of Biologists Ltd.

MeSH Terms (9)

Animals Enterocytes Genetic Diseases, Inborn Intestinal Diseases Mice Mice, Knockout Microvilli Myosin Type V rab GTP-Binding Proteins

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