Investigation of the role intracelluar MST/Krs protein

细胞内MST/Krs蛋白作用的研究

• 批准号: 12672144
• 负责人: WATABE Masahiko
• 金额: $ 2.18万
• 依托单位: SHOWA UNIVERSITY (2001)The Institute of Physical and Chemical Research (2000)
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Scientific Research (C)
• 财政年份: 2000
• 资助国家: 日本
• 起止时间: 2000 至 2001
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-12672144/
• 关键词: Cell Division; Cell Growth; Cell Death; Protein Kinase; MST; Krsタンパク質

Staurosporine and its analogues (K-2S2a, RK-286C) are known to inhibit the protein kinases and also to cause DNA re-replication the same as cytochalasin B in rat diploid fibroblast 3Y1 cells without an intervening mitosis, producing tetraploid cells. We found that these drugs induced the increase of cell size by the inhibition of cell division but not nucleus division in human chronic myelogenous leukemia K562 cells. This phenomenon was expected to the relation of one protein kinase and we found that the human protein kinases, MST1/Krs2 and MST2/Kpsl, related to the cell division on the cell proliferation and might be one of the target factors of those drugs. To examine the importance of MST/Krs in the cell division, we investigated the effect of kinase-inactive MST/Krs expression during the cell proliferation. The expression of kinase-inactive MST/Krs in K562 cells induced the inhibition of cell growth and increase of the cell size was caused by the increase of nucleus count in the cells. Moreover, we performed the double staining with Hoechst 33258 and rhodamine phalloidin, when the kinase-inactive MST/KrS was overexpressed in human cervix epithelioid carcinoma HeLa cells. On the cells expressed kinase-inactive MST/Krs, we observed the increase of the nucleus count and the siassembly of actin filament. These results suggest that MST/Krs is one of the target factors of those drugs and plays the important role on the cell division by the relation to the stability of cytoskeleton protein such as actin.

已知星形孢菌素及其类似物（K-2S 2a、RK-286 C）可抑制蛋白激酶，并与细胞松弛素B一样，在大鼠二倍体成纤维细胞3 Y1细胞中引起DNA再复制，而无中间有丝分裂，产生四倍体细胞。我们发现，这些药物通过抑制细胞分裂而不是核分裂诱导人慢性粒细胞白血病K562细胞的细胞大小的增加。这一现象可能与一种蛋白激酶有关，我们发现人类蛋白激酶MST 1/Krs 2和MST 2/Kps 1与细胞分裂和细胞增殖有关，可能是这些药物的靶向因子之一。为了研究MST/Krs在细胞分裂中的重要性，我们研究了激酶失活的MST/Krs表达在细胞增殖过程中的作用。K562细胞中激酶失活的MST/Krs的表达诱导细胞生长抑制，细胞体积增大是由于细胞核数增加所致。此外，我们进行了双重染色Hoechst 33258和罗丹明鬼笔环肽，当激酶失活MST/KrS在人宫颈上皮样癌HeLa细胞过表达。在表达激酶失活的MST/Krs的细胞上，我们观察到细胞核计数增加和肌动蛋白丝的重新组装。这些结果表明MST/Krs是这些药物的靶向因子之一，并通过与细胞骨架蛋白如肌动蛋白的稳定性相关而在细胞分裂中起重要作用。