Single-Cell RNA-Seq Identifies Dynamic Cardiac Transition Program from ADCs Induced by Leukemia Inhibitory Factor

Author:

Yao Jiayi1,Ma Feiyang23ORCID,Zhang Li1ORCID,Zhu Ching1,Jumabay Medet4,Yao Zehao5,Wang Lumin6,Cai Xinjiang1,Zhang Daoqin1,Qiao Xiaojing1,Shivkumar Kalyanam1,Pellegrini Matteo27,Yao Yucheng1,Wu Xiuju1,Boström Kristina I12ORCID

Affiliation:

1. Division of Cardiology, David Geffen School of Medicine at University of California, Los Angeles , Los Angeles, CA , USA

2. Molecular Biology Institute, University of California, Los Angeles , Los Angeles, CA , USA

3. Chongqing International Institute for Immunology , Chongqing , People’s Republic of China

4. Division of Allergy, Immunology Center for Immunity, Infection, and Inflammation Pediatrics, Dept of Medicine, University of California, San Diego , San Diego, CA , USA

5. Peking Union Medical College, Chinese Academy of Medical Science & Peking Union Medical College , Beijing , People’s Republic of China

6. Institute of Precision Medicine, the Second Affiliated Hospital of Xi’an Jiaotong University , Xi’an , People’s Republic of China

7. Dept of Molecular, Cell and Developmental Biology, University of California, Los Angeles , Los Angeles, CA , USA

Abstract

Abstract Adipose-derived cells (ADCs) from white adipose tissue are promising stem cell candidates because of their large regenerative reserves and the potential for cardiac regeneration. However, given the heterogeneity of ADC and its unsolved mechanisms of cardiac acquisition, ADC-cardiac transition efficiency remains low. In this study, we explored the heterogeneity of ADCs and the cellular kinetics of 39,432 single-cell transcriptomes along the leukemia inhibitory factor (LIF)-induced ADC-cardiac transition. We identified distinct ADC subpopulations that reacted differentially to LIF when entering the cardiomyogenic program, further demonstrating that ADC-myogenesis is time-dependent and initiates from transient changes in nuclear factor erythroid 2-related factor 2 (Nrf2) signaling. At later stages, pseudotime analysis of ADCs navigated a trajectory with 2 branches corresponding to activated myofibroblast or cardiomyocyte-like cells. Our findings offer a high-resolution dissection of ADC heterogeneity and cell fate during ADC-cardiac transition, thus providing new insights into potential cardiac stem cells.

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

NIH

National Institute on Neurological Disorders and Stroke

NHLBI

UCLA Specialty Training and Advanced Research

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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