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DOI 10.3791/59452

Медицинская библиотека · Journal of visualized experiments : JoVE · 2019

Enhancing the Engraftment of Human Induced Pluripotent Stem Cell-derived Cardiomyocytes via a Transient Inhibition of Rho Kinase Activity.

Zhao Meng, Tang Yawen, Ernst Patrick J, Kahn-Krell Asher, Fan Chengming, Pretorius Danielle, Zhu Hanxi, Lou Xi, Zhou Lufang, Zhang Jianyi, Zhu Wuqiang

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАVideo-Audio MediaПеревод в очереди

Аннотация

A crucial factor in improving cellular therapy effectiveness for myocardial regeneration is to safely and efficiently increase the cell engraftment rate. Y-27632 is a highly potent inhibitor of Rho-associated, coiled-coil-containing protein kinase (RhoA/ROCK) and is used to prevent dissociation-induced cell apoptosis (anoikis). We demonstrate that Y-27632 pretreatment for human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs+RI) prior to implantation results in a cell engraftment rate improvement in a mouse model of acute myocardial infarction (MI). Here, we describe a complete procedure of hiPSC-CMs differentiation, purification, and cell pretreatment with Y-27632, as well as the resulting cell contraction, calcium transient measurements, and transplantation into mouse MI models. The proposed method provides a simple, safe, effective, and low-cost method which significantly increases the cell engraftment rate. This method cannot only be used in conjunction with other methods to further enhance the cell transplantation efficiency but also provides a favorable basis for the study of the mechanisms of other cardiac diseases.

Для цитирования: Zhao Meng, Tang Yawen, Ernst Patrick J, Kahn-Krell Asher, Fan Chengming, Pretorius Danielle, Zhu Hanxi, Lou Xi, Zhou Lufang, Zhang Jianyi, Zhu Wuqiang. Enhancing the Engraftment of Human Induced Pluripotent Stem Cell-derived Cardiomyocytes via a Transient Inhibition of Rho Kinase Activity.. Journal of visualized experiments : JoVE. 2019. DOI: 10.3791/59452.

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