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[细胞外信号调节激酶和p38丝裂原活化蛋白激酶的表达与人类精子活力]

[ERK and P38MAPK expressions and human sperm motility].

作者信息

Ding Yu-Qin, Jiang Hong, Wang Cun-Li

机构信息

Reproductive Medicine Center, The PLA Clinical Medical School Affiliated to Anhui Medical University, Hefei, Anhui 230031, China.

出版信息

Zhonghua Nan Ke Xue. 2011 Sep;17(9):809-12.

Abstract

OBJECTIVE

To compare the phosphorylation and protein expression of extracellular-signal regulated protein kinase (ERK) and P38 mitogen activated protein kinase (P38 MAPK) in the ejaculated spermatozoa of healthy volunteers and asthenospermia males, and to explore the correlation of ERK and P38 MAPK with human sperm motility.

METHODS

Semen samples were collected from 20 healthy volunteers (sperm concentration > or = 20 x 10(6)/ml, grade a sperm > or = 25% or grade a + b sperm > or = 50%) and 20 infertile males with asthenospermia (sperm concentration > or = 20 x 10(6)/ml, grade a sperm < 25% and grade a + b sperm < or = 40%) and classified as a control and an asthenospermia group. Total protein in spermatozoa was extracted from all the subjects, and Western blotting was used to detect phosphorylation and protein expression levels of ERK and P38 MAPK.

RESULTS

Compared with the control group, the protein expression levels of ERK and P38 MAPK and the phosphorylation level of P38 MAPK were significantly increased in the asthenospermia group (P < 0.05), but there were no statistically significant differences in the phosphorylation level of ERK between the two groups (P > 0.05).

CONCLUSION

The up-regulated protein expressions of ERK and P38MAPK and increased phosphorylation level of P38 MAPK in human sperm may be involved in the pathogenesis of asthenospermia.

摘要

目的

比较健康志愿者与弱精子症男性射出精子中细胞外信号调节蛋白激酶(ERK)和P38丝裂原活化蛋白激酶(P38 MAPK)的磷酸化水平及蛋白表达,探讨ERK和P38 MAPK与人类精子活力的相关性。

方法

收集20名健康志愿者(精子浓度≥20×10⁶/ml,a级精子≥25%或a + b级精子≥50%)和20名弱精子症不育男性(精子浓度≥20×10⁶/ml,a级精子<25%且a + b级精子≤40%)的精液样本,分为对照组和弱精子症组。提取所有受试者精子中的总蛋白,采用蛋白质印迹法检测ERK和P38 MAPK的磷酸化水平及蛋白表达水平。

结果

与对照组相比,弱精子症组ERK和P38 MAPK的蛋白表达水平及P38 MAPK的磷酸化水平显著升高(P < 0.05),但两组间ERK的磷酸化水平差异无统计学意义(P > 0.05)。

结论

人类精子中ERK和P38 MAPK蛋白表达上调及P38 MAPK磷酸化水平升高可能参与弱精子症的发病机制。

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