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NuMA1 promotes axon initial segment assembly through inhibition of endocytosis.


ABSTRACT: Axon initial segments (AISs) initiate action potentials and regulate the trafficking of vesicles between somatodendritic and axonal compartments. However, the mechanisms controlling AIS assembly remain poorly defined. We performed differential proteomics and found nuclear mitotic apparatus protein 1 (NuMA1) is downregulated in AIS-deficient neonatal mouse brains and neurons. NuMA1 is transiently located at the AIS during development where it interacts with the scaffolding protein 4.1B and the dynein regulator lissencephaly 1 (Lis1). Silencing NuMA1 or protein 4.1B by shRNA disrupts AIS assembly, but not maintenance. Silencing Lis1 or overexpressing NuMA1 during AIS assembly increased the density of AIS proteins, including ankyrinG and neurofascin-186 (NF186). NuMA1 inhibits the endocytosis of AIS NF186 by impeding Lis1's interaction with doublecortin, a potent facilitator of NF186 endocytosis. Our results indicate the transient expression and AIS localization of NuMA1 stabilizes the developing AIS by inhibiting endocytosis and removal of AIS proteins.

SUBMITTER: Torii T 

PROVIDER: S-EPMC7041696 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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NuMA1 promotes axon initial segment assembly through inhibition of endocytosis.

Torii Tomohiro T   Ogawa Yuki Y   Liu Cheng-Hsin CH   Ho Tammy Szu-Yu TS   Hamdan Hamdan H   Wang Chih-Chuan CC   Oses-Prieto Juan A JA   Burlingame Alma L AL   Rasband Matthew N MN  

The Journal of cell biology 20200201 2


Axon initial segments (AISs) initiate action potentials and regulate the trafficking of vesicles between somatodendritic and axonal compartments. However, the mechanisms controlling AIS assembly remain poorly defined. We performed differential proteomics and found nuclear mitotic apparatus protein 1 (NuMA1) is downregulated in AIS-deficient neonatal mouse brains and neurons. NuMA1 is transiently located at the AIS during development where it interacts with the scaffolding protein 4.1B and the dy  ...[more]

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