中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Endocytosis-mediated mitochondrial transplantation: Transferring normal human astrocytic mitochondria into glioma cells rescues aerobic respiration and enhances radiosensitivity

文献类型:期刊论文

作者Wang, Bing2; Wang, Zhenhua3; Liu, Yang1,4,5,6; Di, Cuixia1,4,5,6; Zhang, Hong1,4,5,6; Si, Jing1,4,5,6; Li, Hongyan1,4,5,6; Wu, Qingfeng1; Xu, Dan1; Li, Ji3
刊名THERANOSTICS
出版日期2019
卷号9期号:12页码:3595-3607
ISSN号1838-7640
关键词mitochondrial transplantation NAD(+)-CD38-cADPR-Ca2+ signaling endocytosis energy metabolism radiation therapy gliomas
DOI10.7150/thno.33100
通讯作者Zhang, Hong(zhangh@impcas.ac.cn)
英文摘要Emerging evidence indicates that reprogramming of energy metabolism involving disturbances in energy production from a defect in cellular respiration with a shift to glycolysis is a core hallmark of cancer. Alterations in cancer cell energy metabolism are linked to abnormalities in mitochondrial function. Mitochondrial dysfunction of cancer cells includes increased glycolysis, decreased apoptosis, and resistance to radiotherapy. The study was designed for two main points: firstly, to investigate whether exogenous functional mitochondria can transfer into glioma cells and explore the underlying molecular mechanisms from the perspective of endocytosis; secondly, to further verify whether the mitochondrial transplantation is able to rescue aerobic respiration, attenuate the Warburg effect and enhance the radiosensitivity of gliomas. Methods: Mitochondria were isolated from normal human astrocytes (HA) and immediately co-incubated with starved human glioma cells (U87). Confocal microscopy and gene sequencing were performed to evaluate the ability of isolated mitochondria internalization into U87 cells. The interaction between endocytosis and isolated mitochondria transfer were captured by 3D tomographic microscopy and transmission electron microscopy. NAD(+), CD38, cADPR and Ca2+ release were determined by commercial kits, western blot, HLPC-MS and Fluo-3 AM respectively. PCR array expression profiling and Seahorse XF analysis were used to evaluate the effect of mitochondrial transplantation on energy phenotypes of U87 cells. U87 cells and U87 xenografts were both treated with mitochondrial transplantation, radiation, or a combination of mitochondrial transplantation and radiation. Apoptosis in vitro and in vivo were detected by cytochrome C, cleaved caspase 9 and TUNEL staining. Results: We found that mitochondria from HA could be transferred into starved U87 cells by simple co-incubation. Starvation treatment slowed the rate of glycolysis and decreased the transformation of NAD(+) to NADH in U87 cells. A large amount of accumulated NAD(+) was released into the extracellular space. CD38 is a member of the NAD(+) glycohydrolase family that catalyzes cyclization of extracellular NAD(+) to intracellular cADPR. cADPR triggered release of Ca2+ to promote cytoskeleton remodeling and plasma membrane invagination. Thus, endocytosis involving isolated mitochondria internalization was mediated by NAD(+)-CD38-cADPR-Ca2+ signaling. Mitochondrial transfer enhanced gene and protein expression related to the tricarboxylic acid (TCA) cycle, increased aerobic respiration, attenuated glycolysis, reactivated the mitochondrial apoptotic pathway, inhibited malignant proliferation of U87 cells. Isolated mitochondria injected into U87 xenograft tumors also entered cells, and inhibited glioma growth in nude mice. Mitochondrial transplantation could enhance the radiosensitivity of gliomas in vitro and in vivo. Conclusion: These findings suggested that starvation-induced endocytosis via NAD(+)-CD38-cADPR-Ca2+ signaling could be a new mechanism of mitochondrial transplantation to rescue aerobic respiration and attenuate the Warburg effect. This mechanism could be a promising approach for radiosensitization.
WOS关键词CYCLIC ADP-RIBOSE ; MESENCHYMAL STEM-CELLS ; RYANODINE RECEPTOR ; CANCER ; INTERNALIZATION ; PROLIFERATION ; METABOLISM ; ACTIVATION ; AUTOPHAGY ; MUSCLE
资助项目Ministry of Science and Technology National Key R D Project[SQ2018YFE020524] ; National Natural Science Foundation of China[11775280] ; CAS Light of West China Program[Y866020XB0] ; Natural Science Foundation of Gansu Province[18JR3RA391]
WOS研究方向Research & Experimental Medicine
语种英语
出版者IVYSPRING INT PUBL
WOS记录号WOS:000469953000015
资助机构Ministry of Science and Technology National Key R D Project ; National Natural Science Foundation of China ; CAS Light of West China Program ; Natural Science Foundation of Gansu Province
源URL[http://119.78.100.186/handle/113462/133482]  
专题中国科学院近代物理研究所
通讯作者Zhang, Hong
作者单位1.Chinese Acad Sci, Inst Modern Phys, Lanzhou, Gansu, Peoples R China
2.Natl Inst Quantum & Radiol Sci & Technol, Natl Inst Radiol Sci, Chiba, Japan
3.Yantai Univ, Ctr Mitochondria & Hlth Ageing, Yantai, Peoples R China
4.Univ Chinese Acad Sci, Beijing, Peoples R China
5.Key Lab Heavy Ion Radiat Med Gansu Prov, Lanzhou, Gansu, Peoples R China
6.Chinese Acad Sci, Key Lab Heavy Ion Radiat Med, Lanzhou, Gansu, Peoples R China
推荐引用方式
GB/T 7714
Wang, Bing,Wang, Zhenhua,Liu, Yang,et al. Endocytosis-mediated mitochondrial transplantation: Transferring normal human astrocytic mitochondria into glioma cells rescues aerobic respiration and enhances radiosensitivity[J]. THERANOSTICS,2019,9(12):3595-3607.
APA Wang, Bing.,Wang, Zhenhua.,Liu, Yang.,Di, Cuixia.,Zhang, Hong.,...&Liu, Xiongxiong.(2019).Endocytosis-mediated mitochondrial transplantation: Transferring normal human astrocytic mitochondria into glioma cells rescues aerobic respiration and enhances radiosensitivity.THERANOSTICS,9(12),3595-3607.
MLA Wang, Bing,et al."Endocytosis-mediated mitochondrial transplantation: Transferring normal human astrocytic mitochondria into glioma cells rescues aerobic respiration and enhances radiosensitivity".THERANOSTICS 9.12(2019):3595-3607.

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来源:近代物理研究所

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