Horne Melinda M, Guadagno Thomas M
Department of Interdisciplinary Oncology, H. Lee Moffitt Comprehensive Cancer Center, Tampa, FL 33612, USA.
J Cell Biol. 2003 Jun 23;161(6):1021-8. doi: 10.1083/jcb.200304144.
Circumstantial evidence has suggested the possibility of microtubule-associated protein (MAP) kinase's involvement in spindle regulation. To test this directly, we asked whether MAP kinase was required for spindle assembly in Xenopus egg extracts. Either the inhibition or the depletion of endogenous p42 MAP kinase resulted in defective spindle structures resembling asters or half-spindles. Likewise, an increase in the length and polymerization of microtubules was measured in aster assays suggesting a role for MAP kinase in regulating microtubule dynamics. Consistent with this, treatment of extracts with either a specific MAP kinase kinase inhibitor or a MAP kinase phosphatase resulted in the rapid disassembly of bipolar spindles into large asters. Finally, we report that mitotic progression in the absence of MAP kinase signaling led to multiple spindle abnormalities in NIH 3T3 cells. We therefore propose that MAP kinase is a key regulator of the mitotic spindle.
间接证据表明,微管相关蛋白(MAP)激酶可能参与纺锤体调控。为了直接验证这一点,我们研究了非洲爪蟾卵提取物中纺锤体组装是否需要MAP激酶。内源性p42 MAP激酶的抑制或缺失都会导致纺锤体结构缺陷,类似于星状体或半纺锤体。同样,在星状体实验中检测到微管长度增加和聚合,表明MAP激酶在调节微管动力学中发挥作用。与此一致的是,用特定的MAP激酶激酶抑制剂或MAP激酶磷酸酶处理提取物会导致双极纺锤体迅速解体为大型星状体。最后,我们报告在没有MAP激酶信号传导的情况下,NIH 3T3细胞的有丝分裂进程会导致多个纺锤体异常。因此,我们认为MAP激酶是有丝分裂纺锤体的关键调节因子。