Characterization and modulation of human mesenchymal stem cell stress pathway response following hypothermic storage

被引:18
作者
Corwin, William L. [1 ,2 ]
Baust, John M. [1 ,2 ]
Baust, John G. [2 ,3 ]
Van Buskirk, Robert G. [1 ,2 ,3 ]
机构
[1] CPSI Biotech, Owego, NY 13827 USA
[2] SUNY Binghamton, Inst Biomed Technol, Binghamton, NY 13902 USA
[3] SUNY Binghamton, Dept Biol Sci, Binghamton, NY 13902 USA
关键词
Apoptosis; Necrosis; Mesenchymal stem cell; ER stress; Unfolded protein response; Hypothermic storage; Resveratrol; Salubrinal; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; RESVERATROL; APOPTOSIS; CANCER; ACTIVATION; PROLIFERATION; DEATH;
D O I
10.1016/j.cryobiol.2014.01.014
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Human mesenchymal stem cell (hMSC) research has grown exponentially in the last decade. The ability to process and preserve these cells is vital to their use in stem cell therapy. As such, understanding the complex, molecular-based stress responses associated with biopreservation is necessary to improve outcomes and maintain the unique stem cell properties specific to hMSC. In this study hMSC were exposed to cold storage (4 C) for varying intervals in three different media. The addition of resveratrol or salubrinal was studied to determine if either could improve cell tolerance to cold. A rapid elevation in apoptosis at I h post-storage as well as increased levels of necrosis through the 24 h of recovery was noted in samples. The addition of resveratrol resulted in significant improvements to hMSC survival while the addition of salubrinal revealed a differential response based on the media utilized. Decreases in both apoptosis and necrosis together with decreased cell stress/death signaling protein levels were observed following modulation. Further, ER stress and subsequent unfolded protein response (UPR) stress pathway activation was implicated in response to hMSC hypothermic storage. This study is an important first step in understanding hMSC stress responses to cold exposure and demonstrates the impact of targeted molecular modulation of specific stress pathways on cold tolerance thereby yielding improved outcomes. Continued research is necessary to further elucidate the molecular mechanisms involved in hypothermic-induced hMSC cell death. This study has demonstrated the potential for improving hMSC processing and storage through targeting select cell stress pathways. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:215 / 226
页数:12
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