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使用基于荧光共振能量转移(FRET)的探针观察细胞分裂过程中Rho家族小GTP酶的活性。

Activity of Rho-family GTPases during cell division as visualized with FRET-based probes.

作者信息

Yoshizaki Hisayoshi, Ohba Yusuke, Kurokawa Kazuo, Itoh Reina E, Nakamura Takeshi, Mochizuki Naoki, Nagashima Kazuo, Matsuda Michiyuki

机构信息

Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Japan.

出版信息

J Cell Biol. 2003 Jul 21;162(2):223-32. doi: 10.1083/jcb.200212049. Epub 2003 Jul 14.

Abstract

Rho-family GTPases regulate many cellular functions. To visualize the activity of Rho-family GTPases in living cells, we developed fluorescence resonance energy transfer (FRET)-based probes for Rac1 and Cdc42 previously (Itoh, R.E., K. Kurokawa, Y. Ohba, H. Yoshizaki, N. Mochizuki, and M. Matsuda. 2002. Mol. Cell. Biol. 22:6582-6591). Here, we added two types of probes for RhoA. One is to monitor the activity balance between guanine nucleotide exchange factors and GTPase-activating proteins, and another is to monitor the level of GTP-RhoA. Using these FRET probes, we imaged the activities of Rho-family GTPases during the cell division of HeLa cells. The activities of RhoA, Rac1, and Cdc42 were high at the plasma membrane in interphase, and decreased rapidly on entry into M phase. From after anaphase, the RhoA activity increased at the plasma membrane including cleavage furrow. Rac1 activity was suppressed at the spindle midzone and increased at the plasma membrane of polar sides after telophase. Cdc42 activity was suppressed at the plasma membrane and was high at the intracellular membrane compartments during cytokinesis. In conclusion, we could use the FRET-based probes to visualize the complex spatio-temporal regulation of Rho-family GTPases during cell division.

摘要

Rho家族GTP酶调节多种细胞功能。为了在活细胞中可视化Rho家族GTP酶的活性,我们之前开发了基于荧光共振能量转移(FRET)的Rac1和Cdc42探针(伊藤,R.E.,黑川,K.,大场,Y.,吉崎,H.,望月,N.,松田,M. 2002. 《分子与细胞生物学》22:6582 - 6591)。在此,我们添加了两种针对RhoA的探针。一种用于监测鸟嘌呤核苷酸交换因子和GTP酶激活蛋白之间的活性平衡,另一种用于监测GTP - RhoA的水平。使用这些FRET探针,我们对HeLa细胞分裂过程中Rho家族GTP酶的活性进行了成像。在间期,RhoA、Rac1和Cdc42在质膜上的活性较高,进入M期后迅速下降。从后期开始,RhoA活性在包括分裂沟在内的质膜处增加。Rac1活性在纺锤体中区受到抑制,末期后在极侧质膜处增加。Cdc42活性在质膜处受到抑制,在胞质分裂期间在内膜区室处较高。总之,我们可以使用基于FRET的探针来可视化细胞分裂过程中Rho家族GTP酶复杂的时空调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b59/2172791/7dd33c914384/200212049f1.jpg

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