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Programmed cell death in stem cell-based therapy: Mechanisms and clinical applications.

作者信息

Hu Xi-Min, Zhang Qi, Zhou Rui-Xin, Wu Yan-Lin, Li Zhi-Xin, Zhang Dan-Yi, Yang Yi-Chao, Yang Rong-Hua, Hu Yong-Jun, Xiong Kun

机构信息

Department of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha 410013, Hunan Province, China.

Department of Burns, Fo Shan Hospital of Sun Yat-Sen University, Foshan 528000, Guangdong Province, China.

出版信息

World J Stem Cells. 2021 May 26;13(5):386-415. doi: 10.4252/wjsc.v13.i5.386.


DOI:10.4252/wjsc.v13.i5.386
PMID:34136072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8176847/
Abstract

Stem cell-based therapy raises hopes for a better approach to promoting tissue repair and functional recovery. However, transplanted stem cells show a high death percentage, creating challenges to successful transplantation and prognosis. Thus, it is necessary to investigate the mechanisms underlying stem cell death, such as apoptotic cascade activation, excessive autophagy, inflammatory response, reactive oxygen species, excitotoxicity, and ischemia/hypoxia. Targeting the molecular pathways involved may be an efficient strategy to enhance stem cell viability and maximize transplantation success. Notably, a more complex network of cell death receives more attention than one crucial pathway in determining stem cell fate, highlighting the challenges in exploring mechanisms and therapeutic targets. In this review, we focus on programmed cell death in transplanted stem cells. We also discuss some promising strategies and challenges in promoting survival for further study.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/805c0cf28154/WJSC-13-386-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/e9b31a05c726/WJSC-13-386-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/09d25ff5c150/WJSC-13-386-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/ebe502aafcab/WJSC-13-386-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/d2987717b429/WJSC-13-386-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/6956423ba19b/WJSC-13-386-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/805c0cf28154/WJSC-13-386-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/e9b31a05c726/WJSC-13-386-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/09d25ff5c150/WJSC-13-386-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/ebe502aafcab/WJSC-13-386-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/d2987717b429/WJSC-13-386-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/6956423ba19b/WJSC-13-386-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3fd/8176847/805c0cf28154/WJSC-13-386-g006.jpg

相似文献

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Programmed cell death in stem cell-based therapy: Mechanisms and clinical applications.

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[2]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Bibliometric Analysis of the Inflammasome and Pyroptosis in Brain.

Front Pharmacol. 2021-1-20

[2]
Metformin impairs homing ability and efficacy of mesenchymal stem cells for cardiac repair in streptozotocin-induced diabetic cardiomyopathy in rats.

Am J Physiol Heart Circ Physiol. 2021-4-1

[3]
c-FLIP regulates pyroptosis in retinal neurons following oxygen-glucose deprivation/recovery via a GSDMD-mediated pathway.

Ann Anat. 2021-5

[4]
Research trends, hot spots and prospects for necroptosis in the field of neuroscience.

Neural Regen Res. 2021-8

[5]
Extracellular vesicles derived from mesenchymal stem cells: A platform that can be engineered.

Histol Histopathol. 2021-6

[6]
Multifaceted WNT Signaling at the Crossroads Between Epithelial-Mesenchymal Transition and Autophagy in Glioblastoma.

Front Oncol. 2020-11-12

[7]
Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes.

Cell. 2021-1-7

[8]
The Role of iPSC Modeling Toward Projection of Autophagy Pathway in Disease Pathogenesis: Leader or Follower.

Stem Cell Rev Rep. 2021-4

[9]
Preconditioning Strategies to Enhance Neural Stem Cell-Based Therapy for Ischemic Stroke.

Brain Sci. 2020-11-23

[10]
Tissue Inhibitor of Metalloprotease-1 (TIMP-1) Regulates Adipogenesis of Adipose-derived Stem Cells (ASCs) via the Wnt Signaling Pathway in an MMP-independent Manner.

Curr Med Sci. 2020-10

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