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顶体 Na+-K+-ATP 酶同工酶是否定位于精子头部筏?

Are isoforms of capacitating Na K -ATPase localized to sperm head rafts?

机构信息

Department of Animal and Poultry Science, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Canadian Food Inspection Agency, Lethbridge, Alberta, Canada.

出版信息

Mol Reprod Dev. 2021 Nov;88(11):731-743. doi: 10.1002/mrd.23543. Epub 2021 Oct 17.

DOI:10.1002/mrd.23543
PMID:34658111
Abstract

Capacitation begins in the sperm head plasma membrane (HPM). Membrane rafts could house signaling molecules, but although these specialized microdomains have been microscopically visualized in sperm heads, rafts have been isolated for study only from homogenized whole sperm or tails, never purified HPM. Sodium/potassium ATPase (Na K -ATPase) is a membrane-bound signaling protein that induces capacitation in bull sperm in response to the steroid hormone ouabain, and its subunit isoforms α1, α3, β1, β2, and β3 are known in HPM. This study hypothesized that rafts exist in the HPM of bull sperm, with Na K -ATPase subunit isoforms preferentially localized there. Western immunoblotting (WB) of HPM from fresh, uncapacitated bull sperm (n = 7 ejaculates), and detergent-resistant membranes isolated by density gradient centrifugation from this HPM, contained the raft-marker protein Flotillin-1; the non-raft fraction did not. HPM, raft, and non-raft contained all known Na K -ATPase isoforms including, for the first time, the previously unknown α2 isoform. Quantification (ImageQuant Software) found α3 and β1 were relatively dominant isoforms in the HPM raft. WB profiles of raft isoforms differed significantly from HPM and non-raft profiles, with unique banding patterns and amounts, hinting that the capacitation signaling in the now-identified HPM rafts may depend on unique sequences within the isoform structure.

摘要

获能始于精子头部的质膜(HPM)。膜筏可能容纳信号分子,但尽管这些特化的微区在精子头部已经被显微镜可视化,但只有从匀浆的整个精子或尾部才能分离出筏用于研究,而从未从纯化的 HPM 中分离出来。钠/钾 ATP 酶(Na K -ATPase)是一种膜结合的信号蛋白,它可以诱导牛精子在甾体激素哇巴因的作用下获能,其亚基同工型α1、α3、β1、β2 和β3 在 HPM 中是已知的。本研究假设筏存在于牛精子的 HPM 中,Na K -ATPase 亚基同工型优先定位于那里。新鲜、未获能的公牛精子(n=7 个射精)的 HPM 和通过密度梯度离心从该 HPM 中分离出的去污剂抗性膜的 Western 免疫印迹(WB)含有筏标记蛋白 Flotillin-1;非筏部分没有。HPM、筏和非筏都含有所有已知的 Na K -ATPase 同工型,包括以前未知的α2 同工型。定量(ImageQuant 软件)发现α3 和β1 是 HPM 筏中的相对优势同工型。筏同工型的 WB 谱与 HPM 和非筏谱显著不同,具有独特的带型和数量,暗示现在鉴定的 HPM 筏中的获能信号可能依赖于同工型结构内的独特序列。

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