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氨通过调节Akt/mTOR/S6k信号通路促进骨髓间充质干细胞的增殖。

Ammonia promotes the proliferation of bone marrow-derived mesenchymal stem cells by regulating the Akt/mTOR/S6k pathway.

作者信息

Liu Yu, Zhang Xiangxian, Wang Wei, Liu Ting, Ren Jun, Chen Siyuan, Lu Tianqi, Tie Yan, Yuan Xia, Mo Fei, Yang Jingyun, Wei Yuquan, Wei Xiawei

机构信息

Laboratory of Aging Research and Cancer Drug Target, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, No. 17, Block 3, Southern Renmin Road, Chengdu, Sichuan, 610041, PR China.

Department of Clinical Laboratory, The West China Second University Hospital of Sichuan University (WCSUH-SCU), Sichuan University, No. 17, Block 3, Southern Renmin Road, Chengdu, Sichuan, 610041, PR China.

出版信息

Bone Res. 2022 Aug 26;10(1):57. doi: 10.1038/s41413-022-00215-y.

Abstract

Ammonia plays an important role in cellular metabolism. However, ammonia is considered a toxic product. In bone marrow-derived mesenchymal stem cells, multipotent stem cells with high expression of glutamine synthetase (GS) in bone marrow, ammonia and glutamate can be converted to glutamine via glutamine synthetase activity to support the proliferation of MSCs. As a major nutritional amino acid for biosynthesis, glutamine can activate the Akt/mTOR/S6k pathway to stimulate cell proliferation. The activation of mTOR can promote cell entry into S phase, thereby enhancing DNA synthesis and cell proliferation. Our studies demonstrated that mesenchymal stem cells can convert the toxic waste product ammonia into nutritional glutamine via GS activity. Then, the Akt/mTOR/S6k pathway is activated to promote bone marrow-derived mesenchymal stem cell proliferation. These results suggest a new therapeutic strategy and potential target for the treatment of diseases involving hyperammonemia.

摘要

氨在细胞代谢中起着重要作用。然而,氨被认为是一种有毒产物。在骨髓来源的间充质干细胞中,这种在骨髓中高表达谷氨酰胺合成酶(GS)的多能干细胞,氨和谷氨酸可通过谷氨酰胺合成酶的活性转化为谷氨酰胺,以支持间充质干细胞的增殖。作为生物合成的主要营养氨基酸,谷氨酰胺可激活Akt/mTOR/S6k信号通路以刺激细胞增殖。mTOR的激活可促进细胞进入S期,从而增强DNA合成和细胞增殖。我们的研究表明,间充质干细胞可通过GS活性将有毒废物氨转化为营养性谷氨酰胺。然后,激活Akt/mTOR/S6k信号通路以促进骨髓来源的间充质干细胞增殖。这些结果提示了一种治疗高氨血症相关疾病的新治疗策略和潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fcc/9418171/01f328019101/41413_2022_215_Fig1_HTML.jpg

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