Direct Reprogramming of Fibroblasts into Functional Cardiomyocytes by Defined Factors

The reprogramming of fibroblasts to induced pluripotent stem cells (iPSCs) raises the possibility that a somatic cell could be reprogrammed to an alternative differentiated fate without first becoming a stem/progenitor cell. A large pool of fibroblasts exists in the postnatal heart, yet no single “master regulator” of direct cardiac reprogramming has been identified. Here, we report that a combination of three developmental transcription factors (i.e., Gata4, Mef2c, and Tbx5) rapidly and efficiently reprogrammed postnatal cardiac or dermal fibroblasts directly into differentiated cardiomyocyte-like cells. Induced cardiomyocytes expressed cardiac-specific markers, had a global gene expression profile similar to cardiomyocytes, and contracted spontaneously. Fibroblasts transplanted into mouse hearts one day after transduction of the three factors also differentiated into cardiomyocyte-like cells. We believe these findings demonstrate that functional cardiomyocytes can be directly reprogrammed from differentiated somatic cells by defined factors. Reprogramming of endogenous or explanted fibroblasts might provide a source of cardiomyocytes for regenerative approaches. [Display omitted] [Display omitted] ► Gata4/Mef2c/Tbx5 directly reprogram fibroblasts into cardiomyocyte-like cells ► Induced cardiomyocytes (iCMs) have spontaneous contraction and action potentials ► iCMs resemble cardiomyocytes in their global gene expression and epigenetic state ► Transplanted cardiac fibroblasts can be reprogrammed into iCMs in vivo