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蛋白激酶抑制剂通过使小鼠卵母细胞中的丝裂原活化蛋白激酶失活来诱导间期转变。

Protein kinase inhibitors induce the interphase transition by inactivating mitogen-activated protein kinase in mouse eggs.

作者信息

Sun Q Y, Luria A, Rubinstein S, Breitbart H

机构信息

Bar-Ilan University, Ramat-Gan, Israel.

出版信息

Zygote. 1998 Aug;6(3):277-84. doi: 10.1017/s0967199498000227.

Abstract

The role of mitogen-activated protein (MAP) kinase in mouse egg activation induced by protein kinase inhibitors and a protein tyrosine kinase (PTK) inhibitor was investigated. Separated egg proteins were first probed with anti-Active MAP kinase antibody and then re-probed with anti-ERK2 antibody. Staurosporine and Ro-31-8220, at concentrations that normally inhibit protein kinase C, did not affect egg activation or MAP kinase activity, while higher dosages caused egg activation. Staurosporine at 2 microM induced the metaphase-interphase transition without emission of the second polar body (PB2), while Ro-31-8220 at 40 microM induced PB2 emission, first cleavage, and then the transition to interphase. Half the eggs were also activated by the PTK inhibitor genistein. In each treatment, the proportion of eggs that entered interphase was well correlated with the degree of MAP kinase inactivation. Artificial activation of this kinase by okadaic acid overcame the interphase transition. These data suggest that protein kinase inhibitors and a protein tyrosine kinase inhibitor induce the interphase transition by inactivating MAP kinase in mouse eggs.

摘要

研究了丝裂原活化蛋白(MAP)激酶在蛋白激酶抑制剂和蛋白酪氨酸激酶(PTK)抑制剂诱导的小鼠卵母细胞激活中的作用。首先用抗活性MAP激酶抗体对分离的卵母细胞蛋白进行检测,然后再用抗ERK2抗体进行检测。通常抑制蛋白激酶C的浓度的星形孢菌素和Ro-31-8220不影响卵母细胞激活或MAP激酶活性,而更高剂量则导致卵母细胞激活。2微摩尔的星形孢菌素诱导中期-间期转换,但不释放第二极体(PB2),而40微摩尔的Ro-31-8220诱导PB2释放、第一次卵裂,然后向间期转换。一半的卵母细胞也被PTK抑制剂染料木黄酮激活。在每种处理中,进入间期的卵母细胞比例与MAP激酶失活程度密切相关。用冈田酸人工激活该激酶可克服间期转换。这些数据表明,蛋白激酶抑制剂和蛋白酪氨酸激酶抑制剂通过使小鼠卵母细胞中的MAP激酶失活来诱导间期转换。

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