Crosstalk between one carbon metabolism and eph signaling promotes neural stem cells differentiation through epigenetic remodeling
Metabolic pathways, once seen as a mere consequence of cell states, have emerged as active players in dictating different cellular events such as proliferation, self-renewal and differentiation. Several studies have reported a role for folate-dependent 1-carbon (1C) metabolism in stem cells, however, its exact mode of action and how it interacts with other cues is largely unknown. Here, we report a link between the Eph:ephrin cell-cell communication pathway and 1C metabolism in controlling differentiation of neural stem cells. Transcriptional and functional analyses following ephrin stimulation revealed alterations in folate metabolism-related genes and enzymatic activity. In vitro and in vivo data indicate that Eph-B forward signaling alters the methylation state of H3K4 by regulating 1C metabolism, and locks neural stem cells in a differentiation-ready state. The functional link between cell-cell communication, metabolism and epigenetic remodeling identifies a novel triad in the control of stem cell self-renewal vs. differentiation.\n\nHIGHLIGHTSO_LI1C folate metabolism is regulated by local cell-to-cell communication\nC_LIO_LIDescription of Eph-B transcriptional response in NSC\nC_LIO_LIEph activation decreases the expression and activity of DHFR\nC_LIO_LIInhibition of DHFR modifies epigenetic marks and impairs self-renewal of neural stem cells\nC_LIO_LIDecreased H3K4 methylation locks neural stem cells in a pro-differentiation state\nC_LI\n\neTOC BLURBFawal et al. present evidence that Eph-B forward signaling inhibits 1C folate metabolism in neural stem cells leading to alteration of H3K4 methylation on key progenitor genes. In addition, they show that these epigenetic changes are inherited and maintained in the long term, thus locking NSC into a differentiation ready state.