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佛波酯诱导的K562细胞巨核细胞分化降低了呼吸链复合物IV的活性。

Megakaryocytic differentiation of K562 cells induced by PMA reduced the activity of respiratory chain complex IV.

作者信息

Huang Rui, Zhao Long, Chen Hui, Yin Rong-Hua, Li Chang-Yan, Zhan Yi-Qun, Zhang Jian-Hong, Ge Chang-hui, Yu Miao, Yang Xiao-Ming

机构信息

Beijing Institute of Radiation Medicine, Beijing, China; State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Beijing, China.

出版信息

PLoS One. 2014 May 9;9(5):e96246. doi: 10.1371/journal.pone.0096246. eCollection 2014.

Abstract

Mitochondria are involved in the regulation of cell differentiation processes, but its function changes and molecular mechanisms are not yet clear. In this study, we found that mitochondrial functions changed obviously when K562 cells were induced to megakaryocytic differentiation by phorbol 12-myristate 13-acetate (PMA). During the cell differentiation, the reactive oxygen species (ROS) level was increased, mitochondrial membrane potential declined and respiratory chain complex IV activity was decreased. Treatment with specific inhibitor of mitochondrial respiratory chain complex IV led to a significant inhibition in mitochondrial membrane potential and reduction of PMA-induced cell differentiation. However, treatment with cyclosporine A, a stabilization reagent of mitochondrial membrane potential, did not improve the down-regulation of mitochondrial respiratory chain complex IV induced by PMA. Furthermore, we found that the level of the complex IV core subunit COX3 and mitochondrial transport-related proteins Tim9 and Tim10 were decreased during the differentiation of K562 cells induced by PMA, suggesting an important role of these factors in mitochondrial functional changes. Our results suggest that changes in mitochondrial functions are involved in the PMA-induced K562 cell differentiation process, and the maintenance of the steady-state of mitochondrial functions plays a critical role in the regulation of cell differentiation.

摘要

线粒体参与细胞分化过程的调控,但其功能变化及分子机制尚不清楚。在本研究中,我们发现用佛波酯12 -肉豆蔻酸酯13 -乙酸酯(PMA)诱导K562细胞向巨核细胞分化时,线粒体功能发生明显变化。在细胞分化过程中,活性氧(ROS)水平升高,线粒体膜电位下降,呼吸链复合物IV活性降低。用线粒体呼吸链复合物IV的特异性抑制剂处理导致线粒体膜电位显著抑制,并降低PMA诱导的细胞分化。然而,用线粒体膜电位稳定剂环孢素A处理并不能改善PMA诱导的线粒体呼吸链复合物IV的下调。此外,我们发现PMA诱导K562细胞分化过程中,复合物IV核心亚基COX3以及线粒体转运相关蛋白Tim9和Tim10的水平降低,表明这些因子在线粒体功能变化中起重要作用。我们的结果表明,线粒体功能变化参与了PMA诱导的K562细胞分化过程,线粒体功能稳态的维持在细胞分化调控中起关键作用。

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