Transient Receptor Potential Melastatin Type 7 Channel Is Critical for the Survival of Bone Marrow Derived Mesenchymal Stem Cells

被引:51
作者
Cheng, Henrique [1 ]
Feng, Ji-Ming [1 ]
Figueiredo, Marxa L. [1 ]
Zhang, Hanjie [1 ]
Nelson, Piper L. [1 ]
Marigo, Vanessa [1 ]
Beck, Andreas [2 ]
机构
[1] Louisiana State Univ, Sch Vet Med, Dept Comparat Biomed Sci, Baton Rouge, LA 70803 USA
[2] Univ Saarland, Univ Klinikum, Inst Pharmakol & Toxikol, Saar, Germany
基金
美国国家卫生研究院;
关键词
2-AMINOETHOXYDIPHENYL BORATE 2-APB; SMOOTH-MUSCLE-CELLS; CALCIUM OSCILLATIONS; GENE-EXPRESSION; TRPM7; CHANNEL; MIC CHANNELS; MAGNESIUM; INHIBITION; CURRENTS; GROWTH;
D O I
10.1089/scd.2009.0262
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
The transient receptor potential melastatin type 7 channel (TRPM7) is a member of the TRP family of ion channels that is essential for cell proliferation and viability. Mesenchymal stem cells (MSCs) from bone marrow are a potential source for tissue repair due to their ability to differentiate into specialized cells. However, the role of TRPM7 in stem cells is unknown. In this study, we characterized TRPM7 in mouse MSCs using molecular biology, immunocytochemistry, and patch clamp. We also investigated TRPM7 function using a lentiviral vector and specific shRNA to knockdown gene expression. By RT-PCR and immunocytochemistry, we identified TRPM7, but not TRPM6, a close family member with similar function. Electrophysiological recordings during depletion of intracellular Mg2+ or Mg2+ -ATP resulted in the development of currents typical for the channel. Furthermore, 2-aminoethoxydiphenyl borate (1 pM-100 mu M) inhibited TRPM7 in a concentration-dependent manner. The molecular suppression of TRPM7 significantly decreased MSC proliferation and viability as determined by MTT assay. In addition, TRPM7 gene expression was up-regulated during osteogenesis. These findings demonstrate that TRPM7 is required for MSC survival and perhaps involved in the differentiation process.
引用
收藏
页码:1393 / 1403
页数:11
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