Skip to main content
Fig. 7 | Genome Biology

Fig. 7

From: Programmed genomic instability regulates neural transdifferentiation of human brain microvascular pericytes

Fig. 7

Transdifferentiation efficiency is modulated by exogenous and endogenous cues. a Immunohistochemical identification of NeuN+ transdifferentiated cells in TD-chase experiments wherein pericytes were exposed to neural induction medium (NIM) for 20, 40, and 60 min and then returned to growth medium for 16 h. In TD-chase experiment, NueNhigh/E2F1low profile suggested cell cycle exit and completion of neural lineage reprogramming. Right columns demonstrate the outcome of TD-chase in pericytes conditioned by exposure to hypoxia (t = 30 min) prior to TD. b qPCR quantification of the ratio of ATOH-1 and MASH-1 to MYOD1 as a proxy for TD tendency in pericytes conditioned via serum starvation, hypoxia, and UVC irradiation prior to TD, as per schematic images. X-axis shows time points after the induction of TD. * indicates p < 0.01. c Schematic images summarize the role of exogenous and endogenous cues in programming the transdifferentiation tendency of pericytes. Height of the TD landscape is an approximation of TD propensity of pericytes

Back to article page