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本文引用的文献

1
Profiling of proteins phosphorylated or dephosphorylated during hyperactivation via activation on hamster spermatozoa.通过激活仓鼠精子超活化过程中磷酸化或去磷酸化蛋白质的分析。
Reprod Med Biol. 2006 May 19;5(2):123-135. doi: 10.1007/BF03016148. eCollection 2006 Jun.
2
Effect of fatty acids bound to bovine serum albumin-V on acrosome reaction and utilization of glucose in boar spermatozoa.与牛血清白蛋白-V结合的脂肪酸对猪精子顶体反应及葡萄糖利用的影响。
Reprod Med Biol. 2007 May 14;6(2):109-115. doi: 10.1111/j.1447-0578.2007.00173.x. eCollection 2007 Jun.
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Signalling pathways involved in sperm capacitation.参与精子获能的信号通路。
Soc Reprod Fertil Suppl. 2007;65:245-59.
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Calcium/calmodulin and calmodulin kinase II stimulate hyperactivation in demembranated bovine sperm.钙/钙调蛋白和钙调蛋白激酶II刺激去膜牛精子的超活化。
Biol Reprod. 2005 Sep;73(3):519-26. doi: 10.1095/biolreprod.105.040733. Epub 2005 May 4.
5
Identification of a 71 kDa protein as a putative non-genomic membrane progesterone receptor in boar spermatozoa.鉴定一种71 kDa蛋白为公猪精子中一种假定的非基因组膜孕酮受体。
J Endocrinol. 2005 Feb;184(2):417-25. doi: 10.1677/joe.1.05607.
6
Stimulation of human spermatozoa with progesterone gradients to simulate approach to the oocyte. Induction of [Ca(2+)](i) oscillations and cyclical transitions in flagellar beating.用孕酮梯度刺激人类精子以模拟其向卵母细胞靠近。诱导细胞内钙离子([Ca(2+)](i))振荡以及鞭毛摆动的周期性转变。
J Biol Chem. 2004 Oct 29;279(44):46315-25. doi: 10.1074/jbc.M401194200. Epub 2004 Aug 20.
7
Human spermatozoa as a model for studying membrane receptors mediating rapid nongenomic effects of progesterone and estrogens.人类精子作为研究介导孕酮和雌激素快速非基因组效应的膜受体的模型。
Steroids. 2004 Aug;69(8-9):553-9. doi: 10.1016/j.steroids.2004.05.013.
8
Phospholipase Cdelta4 is required for Ca2+ mobilization essential for acrosome reaction in sperm.磷脂酶Cδ4是精子顶体反应所必需的Ca2+动员所必需的。
J Cell Biol. 2003 Apr 14;161(1):79-88. doi: 10.1083/jcb.200210057.
9
Hyperactivated motility in sperm.精子运动过度活跃。
Reprod Domest Anim. 2003 Apr;38(2):119-24. doi: 10.1046/j.1439-0531.2003.00397.x.
10
Characterization of the intracellular calcium store at the base of the sperm flagellum that regulates hyperactivated motility.对精子鞭毛基部调节超激活运动的细胞内钙库的表征。
Biol Reprod. 2003 May;68(5):1590-6. doi: 10.1095/biolreprod.102.011320. Epub 2002 Nov 27.

孕酮对仓鼠精子超活化的调节。

Regulation of hyperactivation of hamster spermatozoa by progesterone.

作者信息

Noguchi Takao, Fujinoki Masakatsu, Kitazawa Masafumi, Inaba Noriyuki

机构信息

Department of Obstetrics and Gynecology and.

Department of Physiology, School of Medicine, Dokkyo Medical University, Tochigi, Japan.

出版信息

Reprod Med Biol. 2008 Apr 17;7(2):63-74. doi: 10.1111/j.1447-0578.2008.00202.x. eCollection 2008 Jun.

DOI:10.1111/j.1447-0578.2008.00202.x
PMID:29699287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5904637/
Abstract

Although it is accepted that progesterone (P) induces acrosome reaction through non-genomic regulation, it is not well known if P also affects hyperactivation of sperm. Hamster spermatozoa were hyperactivated by incubation for 4 h on modified Tyrode's albumin lactate pyruvate medium and recorded on a DVD via a charge-coupled device camera attached to a microscope with phase-contrast illumination and a small CO incubator. Phosphorylation of proteins was detected by western blotting using antiphosphotyrosine antibodies. Sperm hyperactivation was significantly increased and accelerated by a non-genomic signal of P. Although acceleration of motility of hyperactivated sperm occurred with 10, 20 and 40 ng/mL P, the most effective concentration was 20 ng/mL. Progesterone also significantly increased 80-kDa tyrosine phosphorylation of sperm proteins. Both extracellular Ca and albumin were essential for sperm hyperactivation, and the former was also essential for maintaining sperm flagellar movement. Moreover, phospholipase C (PLC) was associated with the regulation of hyperactivation by P. It is likely that P regulates sperm hyperactivation by a non-genomic signal in relation to tyrosine phosphorylation and PLC. (Reprod Med Biol 2008; : 63-74).

摘要

尽管人们公认孕酮(P)通过非基因组调控诱导顶体反应,但P是否也影响精子超活化尚不清楚。将仓鼠精子在改良的Tyrode白蛋白乳酸丙酮酸培养基上孵育4小时使其超活化,并通过连接到配备相差照明的显微镜和小型CO培养箱的电荷耦合器件相机记录在DVD上。使用抗磷酸酪氨酸抗体通过蛋白质印迹法检测蛋白质的磷酸化。P的非基因组信号显著增加并加速了精子超活化。尽管10、20和40 ng/mL的P都能使超活化精子的运动加速,但最有效的浓度是20 ng/mL。孕酮还显著增加了精子蛋白80-kDa酪氨酸磷酸化。细胞外钙和白蛋白对于精子超活化都是必需的,前者对于维持精子鞭毛运动也是必需的。此外,磷脂酶C(PLC)与P对超活化的调节有关。P可能通过与酪氨酸磷酸化和PLC相关的非基因组信号调节精子超活化。(《生殖医学与生物学》2008年;:63 - 74)