The concept of the plasticity or transdifferentiation of adult stem cells has been challenged by the phenomenon of cell fusion. In this work, we examined whether neonatal cardiomyocytes fuse with various somatic cells including endothelial cells, cardiac fibroblasts, bone marrow cells, and endothelial progenitor cells spontaneously in vitro. When cardiomyocytes were cocultured with endothelial cells or cardiac fibroblasts, they fused and showed phenotypes of cardiomyocytes. Furthermore, cardiomyocytes reentered the G2-M phase in the cell cycle after fusing with proliferative noncardiomyocytes. Transplanted endothelial cells or skeletal muscle–derived cells fused with adult cardiomyocytes in vivo. In the cryoinjured heart, there were Ki67-positive cells that expressed both cardiac and endothelial lineage marker proteins. These results suggest that cardiomyocytes fuse with other cells and enter the cell cycle by maintaining their phenotypes.
Cardiomyocytes fuse with surrounding noncardiomyocytes and reenter the cell cycle
K. Matsuura and H. Wada contributed equally to this paper.
Abbreviations used in this paper: ANF, atrial natriuretic factor; β-gal, β-galactosidase; CAT, chloramphenicol acetyltransferase; cFB, cardiac fibroblasts; cTnT, cardiac troponin T; EPC, endothelial progenitor cell; HUVEC, human umbilical vein endothelial cells; PH3, phosphohistone H3; RFP, red fluorescent protein; UEA-1, ulex europaeus agglutinin-1; vWF, von Willebrand factor.
Katsuhisa Matsuura, Hiroshi Wada, Toshio Nagai, Yoshihiro Iijima, Tohru Minamino, Masanori Sano, Hiroshi Akazawa, Jeffery D. Molkentin, Hiroshi Kasanuki, Issei Komuro; Cardiomyocytes fuse with surrounding noncardiomyocytes and reenter the cell cycle . J Cell Biol 25 October 2004; 167 (2): 351–363. doi: https://doi.org/10.1083/jcb.200312111
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