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如何追踪间充质基质细胞的细胞衰老?

How to track cellular aging of mesenchymal stromal cells?

作者信息

Wagner Wolfgang, Bork Simone, Lepperdinger Günther, Joussen Sylvia, Ma Nan, Strunk Dirk, Koch Carmen

机构信息

Helmholtz Institute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, 52074 Aachen, Germany.

出版信息

Aging (Albany NY). 2010 Apr;2(4):224-30. doi: 10.18632/aging.100136.

Abstract

Mesenchymal stromal cells (MSC) are currently tested in a large number of clinical trials and raise high hope in regenerative medicine. These cells have to be expanded in vitro before transplantation and several studies demonstrated that long-term culture evokes continuous changes in MSC: proliferation rate decays, the cell size increases, differentiation potential is affected, chromosomal instabilities may arise and molecular changes are acquired. Long-term culture of cell preparations might also have therapeutic consequences, although this has hardly been addressed in ongoing trials so far. Reliable therapeutic regimens necessitate quality control of cellular products. This research perspective summarizes available methods to track cellular aging of MSC. We have demonstrated that gene expression changes and epigenetic modifications are continuously acquired during replicative senescence. Molecular analysis of a suitable panel of genes might provide a robust tool to assess efficiency and safety of long-term expansion.

摘要

间充质基质细胞(MSC)目前正在大量临床试验中接受测试,并在再生医学领域带来了很高的期望。这些细胞在移植前必须在体外进行扩增,多项研究表明,长期培养会引起MSC的持续变化:增殖速率下降、细胞大小增加、分化潜能受到影响、可能出现染色体不稳定并获得分子变化。细胞制剂的长期培养也可能产生治疗后果,尽管目前正在进行的试验中几乎没有涉及这一点。可靠的治疗方案需要对细胞产品进行质量控制。本研究展望总结了追踪MSC细胞衰老的现有方法。我们已经证明,在复制性衰老过程中会不断获得基因表达变化和表观遗传修饰。对一组合适基因进行分子分析可能会提供一个强大的工具,以评估长期扩增的效率和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/564a/2881510/7d0a8c93f004/aging-02-224-g001.jpg

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