drosophila sperm swim backwards in the female reproductive tract and are activated via trpp2 ion channels果蝇精子游泳向后在女性生殖系统和通过trpp2离子通道被激活.pdfVIP

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drosophila sperm swim backwards in the female reproductive tract and are activated via trpp2 ion channels果蝇精子游泳向后在女性生殖系统和通过trpp2离子通道被激活.pdf

drosophila sperm swim backwards in the female reproductive tract and are activated via trpp2 ion channels果蝇精子游泳向后在女性生殖系统和通过trpp2离子通道被激活

Drosophila Sperm Swim Backwards in the Female Reproductive Tract and Are Activated via TRPP2 Ion Channels ¨ 1,2 .¤ .¤ 1. 1 1 2 Michael Kottgen * , Alexis Hofherr , Weizhe Li , Kristy Chu , Stacey Cook , Craig Montell , Terry Watnick1* 1 Division of Nephrology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America, 2 Departments of Biological Chemistry and Neuroscience, Center for Sensory Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America Abstract Background: Sperm have but one purpose, to fertilize an egg. In various species including Drosophila melanogaster female sperm storage is a necessary step in the reproductive process. Amo is a homolog of the human transient receptor potential channel TRPP2 (also known as PKD2), which is mutated in autosomal dominant polycystic kidney disease. In flies Amo is required for sperm storage. Drosophila males with Amo mutations produce motile sperm that are transferred to the uterus but they do not reach the female storage organs. Therefore Amo appears to be a mediator of directed sperm motility in the female reproductive tract but the underlying mechanism is unknown. Methodology/Principal Findings: Amo exhibits a unique expression pattern during spermatogenesis. In spermatocytes, Amo is restricted to the endoplasmic reticulum (ER) whereas in mature sperm, Amo clusters at the distal tip of the sperm tail. Here we show that flagellar localization of Amo is required for sperm storage. This raised the question of how Amo at the rear end of sperm regulates forward movement into the storage organs. In order to address this question, we used in vivo imaging of dual

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