| Literature DB >> 31218450 |
Romain Da Costa1,2, Morgane Bordessoules3,4, Magali Guilleman5, Virginie Carmignac3,6, Vincent Lhussiez3, Hortense Courot3, Amandine Bataille7, Amandine Chlémaire7, Céline Bruno3,5, Patricia Fauque3,5, Christel Thauvin3,4,8, Laurence Faivre3,4,9, Laurence Duplomb3,4.
Abstract
The sperm acrosome is a lysosome-related organelle that develops using membrane trafficking from the Golgi apparatus as well as the endolysosomal compartment. How vesicular trafficking is regulated in spermatids to form the acrosome remains to be elucidated. VPS13B, a RAB6-interactor, was recently shown involved in endomembrane trafficking. Here, we report the generation of the first Vps13b-knockout mouse model and show that male mutant mice are infertile due to oligoasthenoteratozoospermia. This phenotype was explained by a failure of Vps13b deficient spermatids to form an acrosome. In wild-type spermatids, immunostaining of Vps13b and Rab6 revealed that they transiently locate to the acrosomal inner membrane. Spermatids lacking Vps13b did not present with the Golgi structure that characterizes wild-type spermatids and showed abnormal targeting of PNA- and Rab6-positive Golgi-derived vesicles to Eea1- and Lamp2-positive structures. Altogether, our results uncover a function of Vps13b in the regulation of the vesicular transport between Golgi apparatus, acrosome, and endolysosome.Entities:
Keywords: Acrosomogenesis; Endosome; Globozoospermia; Lysosome; Male infertility; Oligospermia; Spermatogenesis; Spermiogenesis; Vesicular transport
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Year: 2019 PMID: 31218450 DOI: 10.1007/s00018-019-03192-4
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261