Ice-age endurance: the effects of cryopreservation on proteins of sperm of common carp, Cyprinus carpio L

文献类型： 外文期刊

第一作者： Li, P.

作者： Li, P.;Hulak, M.;Dzyuba, B.;Boryshpolets, S.;Rodina, M.;Gela, D.;Linhart, O.;Koubek, P.;Manaskova-Postlerova, P.;Peknicova, J.;Sulc, M.;Li, P.;Dzyuba, B.

作者机构：

关键词： transferrin: expression;phosphoglycerate kinase 1: expression;S-adenosylhomocysteine hydrolase: 9055-10-1;expression;annexin A4: expression;lactate dehydrogenase B: expression;N-ethylmaleimide-sensitive fusion protein attachment protein alph;a: expression;cofilin 2: expression;transaldolase 1: expression;esterase D-formyl-glutathione hydrolase: expression;membrane trafficking;signal transduction;cell metabolism;cell movement;freeze-thaw process;oxidoreductase activity;quantitative alteration;cryopreservation effect;ice-age endurance;ova hatching rate

期刊名称：THERIOGENOLOGY （ 影响因子：2.74； 五年影响因子：2.93 ）

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年卷期：

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收录情况： SCI

摘要： Damage to spermatozoa during cryopreservation is regarded as a major obstacle to the expansion of sperm storage technology. The authors used two-dimensional polyacrylamide gel electrophoresis and matrix-associated laser desorption/ionization time-of-flight mass spectrometry to explore whether the protein profile of common carp (Cypriot's carpio) spermatozoa is affected by cryopreservation. Fourteen protein spots were significantly altered following cryopreservation. Eleven of these were identified: three as specific membrane proteins (N-ethylmaleimide-sensitive fusion protein attachment protein alpha, cofilin 2, and annexin A4) involved in membrane trafficking, organization, and cell movement; six as cytoplasmic enzymes (S-Adenosylhomocysteine hydrolase, Si:dkey-180p18.9 protein, lactate dehydrogenase B, phosphoglycerate kinase 1, transaldolase 1, and esterase D/formyl-glutathione hydrolase) involved in cell metabolism, oxidoreductase activity, and signal transduction; and two as transferrin variant C and F. Based on these findings, the authors hypothesize that transferrin in cryopreserved sperm may protect spermatozoa against oxidative damage during the freeze-thaw process. Cryopreservation caused changes in spermatozoa protein profiles that may lead to decreased spermatozoa velocity, motility, and fertilization success, and to subsequent ova hatching rate. Crown Copyright (C) 2010 Published by Elsevier Inc. All rights reserved.

分类号： Q95

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