Cdc42 negatively regulates endocytosis during apical membrane maintenance in live animals

Author:

Shitara Akiko1,Malec Lenka1,Ebrahim Seham1,Chen Desu12,Bleck Christopher3,Hoffman Matthew P.4,Weigert Roberto15

Affiliation:

1. Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892

2. College of Computer, Mathematical, and Natural Sciences, University of Maryland, College Park, MD 20742

3. Electron Microscopy Core Facility, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892

4. Matrix and Morphogenesis Section, National Institutes of Health, Bethesda, MD 20892

5. Intracellular Membrane Trafficking Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892

Abstract

Lumen establishment and maintenance are fundamental for tubular organs physiological functions. Most of the studies investigating the mechanisms regulating this process have been carried out in cell cultures or in smaller organisms, whereas little has been done in mammalian model systems in vivo. Here we used the salivary glands of live mice to examine the role of the small GTPase Cdc42 in the regulation of the homeostasis of the intercellular canaliculi, a specialized apical domain of the acinar cells, where protein and fluid secretion occur. Depletion of Cdc42 in adult mice induced a significant expansion of the apical canaliculi, whereas depletion at late embryonic stages resulted in a complete inhibition of their postnatal formation. In addition, intravital subcellular microscopy revealed that reduced levels of Cdc42 affected membrane trafficking from and toward the plasma membrane, highlighting a novel role for Cdc42 in membrane remodeling through the negative regulation of selected endocytic pathways.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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