Genetic lineage tracing identifies in situ Kit-expressing cardiomyocytes

Qiaozhen Liu(Chinese Academy of Sciences), Rui Yang(Shanghai Institutes for Biological Sciences), Xiuzhen Huang(Shanghai Institutes for Biological Sciences), Hui Zhang(Shanghai Institutes for Biological Sciences), Lingjuan He(Shanghai Institutes for Biological Sciences), Libo Zhang(Zhejiang University), Xueying Tian(Chinese Academy of Sciences), Yu Nie(Chinese Academy of Medical Sciences & Peking Union Medical College), Shengshou Hu(Chinese Academy of Medical Sciences & Peking Union Medical College), Yan Yan(Sun Yat-sen University), Li Zhang(Zhejiang University), Zengyong Qiao(Southern Medical University), Qing‐Dong Wang(AstraZeneca (Sweden)), Kathy O. Lui(Chinese University of Hong Kong), Bin Zhou(Chinese Academy of Sciences)
Cell Research
December 4, 2015
Cited by 141Open Access
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Abstract

Cardiac cells marked by c-Kit or Kit, dubbed cardiac stem cells (CSCs), are in clinical trials to investigate their ability to stimulate cardiac regeneration and repair. These studies were initially motivated by the purported cardiogenic activity of these cells. Recent lineage tracing studies using Kit promoter to drive expression of the inducible Cre recombinase showed that these CSCs had highly limited cardiogenic activity, inadequate to support efficient cardiac repair. Here we reassess the lineage tracing data by investigating the identity of cells immediately after Cre labeling. Our instant lineage tracing approach identifies Kit-expressing cardiomyocytes, which are labeled immediately after tamoxifen induction. In combination with long-term lineage tracing experiments, these data reveal that the large majority of long-term labeled cardiomyocytes are pre-existing Kit-expressing cardiomyocytes rather than cardiomyocytes formed de novo from CSCs. This study presents a new interpretation for the contribution of Kit(+) cells to cardiomyocytes and shows that Kit genetic lineage tracing over-estimates the cardiogenic activity of Kit(+) CSCs.


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