Inhibition of neural stem cell aging through the transient induction of reprogramming factors
Autor: | Joonhyuk Choi, Sang Jun Uhm, Jeong Tae Do, Won Ji Lee, Yean Ju Hong, Min Ji Han, Youngsok Choi |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Mice Transgenic Biology Activating Transcription Factor 4 Proinflammatory cytokine Mice 03 medical and health sciences 0302 clinical medicine Neural Stem Cells Pregnancy Animals Transcription factor Cells Cultured Cellular Senescence Embryonic Stem Cells POU domain General Neuroscience ATF4 Cell Differentiation Cellular Reprogramming Endoplasmic Reticulum Stress Neural stem cell Cell biology 030104 developmental biology Female Inflammation Mediators Reprogramming 030217 neurology & neurosurgery Adult stem cell |
Zdroj: | Journal of Comparative Neurology. 529:595-604 |
ISSN: | 1096-9861 0021-9967 |
DOI: | 10.1002/cne.24967 |
Popis: | Adult stem cells age during long-term in vitro culture, and neural stem cells (NSCs), which can self-renew and differentiate into neurons and glial cells, also display reduced differentiation potential after repeated passaging. However, the mechanistic details underlying this process remain unclear. In this study, we found that long-term in vitro culture of NSCs resulted in aging-related upregulation of inflammatory- and endoplasmic reticulum (ER) stress-related genes, including the proinflammatory cytokines interleukin (IL)1β and IL6, the senescence-associated enzyme matrix metallopeptidase 13 (MMP13), and the ER stress-responsive transcription factor activating transcription factor 4 (ATF4) and C/EBP homologous protein (CHOP). However, the cyclic and transient induction of four reprogramming factors (POU domain, class 5, transcription factor 1, also known as octamer-binding transcription factor 4; SRY [sex determining region Y]-box 2; Kruppel-like factor 4; and myelocytomatosis oncogene; collectively referred to as OSKM) can inhibit NSC aging, as indicated by the decreased expression of the inflammatory and ER stress-related genes. We used ROSA-4F NSCs, which express OSKM from only one allele, to minimize the potential for full reprogramming or tumor formation during NSC rejuvenation. We expect that this novel rejuvenation method will enhance the potential of NSCs as a clinical approach to the treatment of neurological diseases. |
Databáze: | OpenAIRE |
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