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人精子质膜磷酯酰丝氨酸易位:质膜区域拓扑学及与细胞活力的关系。

Phosphatidylserine membrane translocation in human spermatozoa: topography in membrane domains and relation to cell vitality.

机构信息

Department of Cell Biology, University of Medical Sciences, Rokietnicka 5D, 60-806 Poznan, Poland.

出版信息

J Membr Biol. 2011 Apr;240(3):165-70. doi: 10.1007/s00232-011-9357-7. Epub 2011 Mar 27.

DOI:10.1007/s00232-011-9357-7
PMID:21442408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3069321/
Abstract

The complex structure of the human spermatozoa membrane comprises five topographic domains. Transmembrane asymmetry of the distribution of phospholipids including phosphatidylserine (PS) is considered a marker of cell activity. The objective of the study was to determine which cytomembrane domains of human spermatozoa are involved in PS membrane translocation and to identify the possible relationship of PS translocation with spermatozoa morphology and vitality. In normozoospermic semen of 35 donors, annexin-V labeling with fluorescein determined PS translocation. Propidium iodide staining distinguished between vital and dead spermatozoa. Three types of PS membrane translocation have been distinguished: (1) in the midpiece, (2) in the acrosomal part and (3) simultaneously in the midpiece and acrosomal part. In morphologically normal vital spermatozoa, PS translocation occurred in the midpiece but never in the equatorial region. In dead spermatozoa, simultaneous PS translocation in the midpiece and acrosomal part was most often observed. The difference between proportions of, respectively, vital and dead spermatozoa presenting PS translocation located in different domains was significant (P < 0.0001). In vital cells, there was no difference in PS translocation prevalence between morphologically normal and abnormal spermatozoa (P > 0.05). The strict relation of PS translocation to specific membrane domains indicates functional specificity. It seems doubtful to include this phenomenon in physiological mechanisms of elimination of abnormal spermatozoa.

摘要

人类精子膜的复杂结构包含五个拓扑区域。包括磷脂酰丝氨酸 (PS) 在内的磷脂的跨膜分布的不对称性被认为是细胞活性的标志。本研究的目的是确定人类精子的哪些细胞质膜域参与 PS 膜易位,并确定 PS 易位与精子形态和活力的可能关系。在 35 名供体的正常精子中,用荧光素标记的 annexin-V 确定 PS 易位。碘化丙啶染色区分活精子和死精子。已经区分出三种类型的 PS 膜易位:(1) 在中段,(2) 在顶体部分,(3) 同时在中段和顶体部分。在形态正常的活精子中,PS 易位发生在中段,但从不发生在赤道区。在死精子中,最常观察到中段和顶体部分同时发生 PS 易位。分别位于不同区域的 PS 易位的活精子和死精子的比例差异具有统计学意义 (P < 0.0001)。在活细胞中,形态正常和异常精子的 PS 易位发生率没有差异 (P > 0.05)。PS 易位与特定膜域的严格关系表明其功能的特异性。将这种现象纳入异常精子消除的生理机制似乎值得怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/b748344c4fe7/232_2011_9357_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/897f8214a7dc/232_2011_9357_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/1e05d920d207/232_2011_9357_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/b748344c4fe7/232_2011_9357_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/897f8214a7dc/232_2011_9357_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/1e05d920d207/232_2011_9357_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05cb/3069321/b748344c4fe7/232_2011_9357_Fig3_HTML.jpg

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