4.8 Review

Current Strategies and Challenges for Purification of Cardiomyocytes Derived from Human Pluripotent Stem Cells

Journal

THERANOSTICS
Volume 7, Issue 7, Pages 2067-2077

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/thno.19427

Keywords

Cardiomyocytes; hPSCs

Funding

  1. Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Korean government (MSIP) [2015M3A9C6031514]
  2. Korea Health Technology R&D Project through Korea Health Industry Development Institute (KHIDI)
  3. Ministry of Health & Welfare, Republic of Korea [HI15C2782, HI16C2211]
  4. NHLBI [R01HL127759, R01HL129511]
  5. NIDDK [DP3-DK108245]
  6. CityU Start-up Grant [7200492]
  7. CityU Research Project [9610355]
  8. Georgia Immuno Engineering Consortium through Georgia Institute of Technology, Emory University
  9. Georgia Research Alliance
  10. Korea Health Promotion Institute [HI16C2211010017] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

Cardiomyocytes (CMs) derived from human pluripotent stem cells (hPSCs) are considered a most promising option for cell-based cardiac repair. Hence, various protocols have been developed for differentiating hPSCs into CMs. Despite remarkable improvement in the generation of hPSC-CMs, without purification, these protocols can only generate mixed cell populations including undifferentiated hPSCs or non-CMs, which may elicit adverse outcomes. Therefore, one of the major challenges for clinical use of hPSC-CMs is the development of efficient isolation techniques that allow enrichment of hPSC-CMs. In this review, we will discuss diverse strategies that have been developed to enrich hPSC-CMs. We will describe major characteristics of individual hPSC-CM purification methods including their scientific principles, advantages, limitations, and needed improvements. Development of a comprehensive system which can enrich hPSC-CMs will be ultimately useful for cell therapy for diseased hearts, human cardiac disease modeling, cardiac toxicity screening, and cardiac tissue engineering.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available