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规模化生产临床级分化人心肌细胞用于再生治疗。

Scalable manufacturing of clinical-grade differentiated cardiomyocytes derived from human-induced pluripotent stem cells for regenerative therapy.

机构信息

Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Cell Prolif. 2022 Aug;55(8):e13248. doi: 10.1111/cpr.13248. Epub 2022 May 9.

Abstract

Basic research on human pluripotent stem cell (hPSC)-derived cardiomyocytes (CMs) for cardiac regenerative therapy is one of the most active and complex fields to achieve this alternative to heart transplantation and requires the integration of medicine, science, and engineering. Mortality in patients with heart failure remains high worldwide. Although heart transplantation is the sole strategy for treating severe heart failure, the number of donors is limited. Therefore, hPSC-derived CM (hPSC-CM) transplantation is expected to replace heart transplantation. To achieve this goal, for basic research, various issues should be considered, including how to induce hPSC proliferation efficiently for cardiac differentiation, induce hPSC-CMs, eliminate residual undifferentiated hPSCs and non-CMs, and assess for the presence of residual undifferentiated hPSCs in vitro and in vivo. In this review, we discuss the current stage of resolving these issues and future directions for realizing hPSC-based cardiac regenerative therapy.

摘要

人多能干细胞(hPSC)衍生的心肌细胞(CMs)用于心脏再生治疗的基础研究是实现这一替代心脏移植的最活跃和最复杂的领域之一,需要整合医学、科学和工程。全球心力衰竭患者的死亡率仍然很高。尽管心脏移植是治疗严重心力衰竭的唯一策略,但供体数量有限。因此,hPSC 衍生的 CM(hPSC-CM)移植有望替代心脏移植。为了实现这一目标,对于基础研究,应该考虑各种问题,包括如何有效地诱导 hPSC 增殖以进行心脏分化,诱导 hPSC-CMs,消除残留的未分化 hPSC 和非-CMs,并评估体外和体内残留的未分化 hPSC 的存在。在这篇综述中,我们讨论了解决这些问题的当前阶段和实现基于 hPSC 的心脏再生治疗的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d9e/9357358/3a6ab35e9701/CPR-55-e13248-g002.jpg

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