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牛精浆磷脂结合蛋白刺激附睾精子的磷脂外流。

Bovine seminal plasma phospholipid-binding proteins stimulate phospholipid efflux from epididymal sperm.

作者信息

Thérien I, Moreau R, Manjunath P

机构信息

Department of Medicine, University of Montreal and Guy-Bernier Research Center, Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada H1T 2M4.

出版信息

Biol Reprod. 1999 Sep;61(3):590-8. doi: 10.1095/biolreprod61.3.590.

Abstract

Several studies have shown that sperm capacitation was accompanied by a change in the lipid composition of the sperm membrane. In cattle, the major proteins of (bovine)seminal plasma (BSP proteins: BSP-A1/A2, BSP-A3, and BSP-30-kDa) potentiate sperm capacitation induced by high-density lipoprotein (HDL). Our recent studies indicate that these proteins and HDL stimulate sperm cholesterol efflux during capacitation. In order to gain more insight into the mechanisms of BSP-mediated sperm capacitation, we studied whether or not BSP proteins induce phospholipid efflux from epididymal sperm membrane. By direct determination of choline phospholipids on unlabeled epididymal sperm, the results show that sperm incubated in the presence of BSP-A1/A2 protein lost 34.4% of their choline phospholipids compared with the control (11.5%). Similar results were obtained using labeled epididymal sperm. Labeling was carried out by incubating washed epididymal sperm for 1 h with medium containing [(3)H]palmitic acid. The majority of the label was incorporated into sperm phosphatidylcholine. Studies of sperm phospholipid efflux were done by incubating the labeled sperm with purified BSP proteins, delipidated BSA, or bovine seminal ribonuclease (RNase, control protein). When labeled ([(3)H]phospholipid) epididymal sperm were incubated with BSP proteins (20-120 microg/ml) for 8 h, the sperm lost [(3)H]phospholipid in a dose-dependent manner (maximum efflux of approximately 30%). After the incubation with BSP proteins, the efflux particles were fractionated by size-exclusion chromatography. Analysis of the fractions obtained showed that the [(3)H]phospholipid was associated with BSP proteins. BSA (6 mg/ml) stimulated a specific phospholipid efflux of approximately 22%. In contrast, bovine RNase (120 microg/ml) did not stimulate phospholipid efflux. These results indicate that BSP proteins participate in the sperm cholesterol and phospholipid efflux that occurs during capacitation.

摘要

多项研究表明,精子获能伴随着精子膜脂质成分的变化。在牛中,(牛)精浆的主要蛋白质(BSP蛋白:BSP-A1/A2、BSP-A3和BSP-30-kDa)可增强高密度脂蛋白(HDL)诱导的精子获能。我们最近的研究表明,这些蛋白质和HDL在获能过程中刺激精子胆固醇外流。为了更深入了解BSP介导的精子获能机制,我们研究了BSP蛋白是否诱导附睾精子膜的磷脂外流。通过直接测定未标记附睾精子上的胆碱磷脂,结果显示,与对照组(11.5%)相比,在BSP-A1/A2蛋白存在下孵育的精子失去了34.4%的胆碱磷脂。使用标记的附睾精子也获得了类似结果。标记是通过将洗涤后的附睾精子与含有[³H]棕榈酸的培养基孵育1小时进行的。大部分标记物掺入精子磷脂酰胆碱中。精子磷脂外流的研究是通过将标记的精子与纯化的BSP蛋白、脱脂牛血清白蛋白(BSA)或牛精核糖核酸酶(RNase,对照蛋白)孵育来进行的。当标记的([³H]磷脂)附睾精子与BSP蛋白(20-120μg/ml)孵育8小时时,精子以剂量依赖方式失去[³H]磷脂(最大外流约为30%)。与BSP蛋白孵育后,通过尺寸排阻色谱法对外流颗粒进行分级分离。对所得级分的分析表明,[³H]磷脂与BSP蛋白相关。BSA(6mg/ml)刺激了约22%的特异性磷脂外流。相比之下,牛RNase(120μg/ml)未刺激磷脂外流。这些结果表明,BSP蛋白参与了获能过程中发生的精子胆固醇和磷脂外流。

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