2. Academic Validation
  3. Single-cell analysis reveals an Angpt4-initiated EPDC-EC-CM cellular coordination cascade during heart regeneration

Single-cell analysis reveals an Angpt4-initiated EPDC-EC-CM cellular coordination cascade during heart regeneration

  • Protein Cell. 2023 May 8;14(5):350-368. doi: 10.1093/procel/pwac010.
Zekai Wu 1,  Yuan Shi 1,  Yueli Cui 1 2,  Xin Xing 3,  Liya Zhang 1,  Da Liu 1,  Yutian Zhang 1,  Ji Dong 1 2,  Li Jin 4,  Meijun Pang 5,  Rui-Ping Xiao 4,  Zuoyan Zhu 1,  Jing-Wei Xiong 5,  Xiangjun Tong 1,  Yan Zhang 4 6,  Shiqiang Wang 3,  Fuchou Tang 1 2,  Bo Zhang 1
Affiliations

Affiliations

  • 1 Key Laboratory of Cell Proliferation and Differentiation of the Ministry of Education, Peking University Genome Editing Research Center, College of Life Sciences, Peking University, Beijing 100871, China.
  • 2 Beijing Advanced Innovation Center for Genomics (ICG), College of Life Sciences, Peking University, Beijing 100871, China.
  • 3 State Key Laboratory of Membrane Biology, College of Life Sciences, Peking University, Beijing 100871, China.
  • 4 State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing 100871, China.
  • 5 Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing 100871, China.
  • 6 Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, School of Basic Medical Sciences, Ministry of Education, Peking University Health Science Center, Beijing 100191, China.
PMID: 37155312 DOI: 10.1093/procel/pwac010
Abstract

Mammals exhibit limited heart regeneration ability, which can lead to heart failure after myocardial infarction. In contrast, zebrafish exhibit remarkable cardiac regeneration capacity. Several cell types and signaling pathways have been reported to participate in this process. However, a comprehensive analysis of how different cells and signals interact and coordinate to regulate cardiac regeneration is unavailable. We collected major cardiac cell types from zebrafish and performed high-precision single-cell transcriptome analyses during both development and post-injury regeneration. We revealed the cellular heterogeneity as well as the molecular progress of cardiomyocytes during these processes, and identified a subtype of atrial cardiomyocyte exhibiting a stem-like state which may transdifferentiate into ventricular cardiomyocytes during regeneration. Furthermore, we identified a regeneration-induced cell (RIC) population in the epicardium-derived cells (EPDC), and demonstrated Angiopoietin 4 (Angpt4) as a specific regulator of heart regeneration. angpt4 expression is specifically and transiently activated in RIC, which initiates a signaling cascade from EPDC to endocardium through the Tie2-MAPK pathway, and further induces activation of Cathepsin K in cardiomyocytes through RA signaling. Loss of angpt4 leads to defects in scar tissue resolution and cardiomyocyte proliferation, while overexpression of angpt4 accelerates regeneration. Furthermore, we found that ANGPT4 could enhance proliferation of neonatal rat cardiomyocytes, and promote cardiac repair in mice after myocardial infarction, indicating that the function of Angpt4 is conserved in mammals. Our study provides a mechanistic understanding of heart regeneration at single-cell precision, identifies Angpt4 as a key regulator of cardiomyocyte proliferation and regeneration, and offers a novel therapeutic target for improved recovery after human heart injuries.

Keywords

Angpt4; EPDC; heart regeneration; scRNA-seq; zebrafish.

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