Cloche/Npas4l is a pro-regenerative platelet factor during zebrafish heart regeneration
Junjie HouiD, Yabing SongiD, Chenglu Xiao, Yuanyuan Sun, Jie SheniD, Xiaokai MaiD, Qinchao Zhou, Shih-Ching Chiu, Yang XuiD, Yanyi HuangiD, Ye‐Guang CheniD, Xiaojun ZhuiD, Jianbin WangiD, Jing-Wei Xiong
Abstract
Zebrafish has full capacity of heart regeneration, but little is known about how blood cells, especially platelets, are involved in this regenerative process. Here we report that cloche/npas4l is a pro-regenerative platelet factor for heart regeneration. We found that haploinsufficiency of npas4l disrupted cardiomyocyte (CM) and endothelial cell (EC) proliferation and heart regeneration after injury. A single-cell transcriptomic atlas revealed that npas4l was dynamically expressed in platelets after heart injury and regulated robust interactions between platelets-CMs or -ECs. Decreasing platelets by either nitroreductase-mediated platelet depletion or platelet-deficient mutant mpl impaired CM and EC proliferation, and over-expression of npas4l in platelets sufficiently induced CM and EC proliferation in uninjured hearts, as well as rescued CM and EC proliferation defects in cloche mutants. Mechanistically, Npas4l positively regulated a panel of ligands expression including bmp6 in platelets to fine-tune CM proliferation and heart regeneration. Therefore, this work unveils a novel platelet Npas4l signaling and presents mechanisms on how platelets modulate CM/EC proliferation via ligand-receptor network during zebrafish heart regeneration.
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