The regulation of muscle stem cell (MuSC) asymmetric division plays an essential role in controlling the growth and repair of skeletal muscle. Perturbations in MuSC function have been demonstrated in disease and aging contexts such as Duchenne’s Muscular Dystrophy (DMD) and sarcopenia. We developed and optimized a high content analysis platform combining lineage tracing, myofiber culture, imaging, and bioinformatic analysis to determine modulators of muscle stem cell division. We discover kinase domain receptor (KDR) as a positive modulator of MuSC asymmetric division and confirmed its expression in satellite cells by ddPCR and immunofluorescence. Knockdown of KDR significantly reduces the numbers of asymmetric divisions, whereas ligand stimulation of KDR increases the numbers of asymmetric divisions. KDR signaling is impaired in dystrophin- deficient satellite cells and requires a polarized cell environment established by the dystrophin glycoprotein complex (DGC) to direct asymmetric division. Mice lacking KDR in MuSCs exhibit reduced numbers of satellite cells due to precocious differentiation, and deficits in regeneration consistent with impaired asymmetric division and reduced generation of progenitors. Therefore, our experiments identify KDR signaling as playing an essential role in MuSC function in muscle regeneration. These findings further our understanding of muscle stem cell biology, and in particular, the role of asymmetric division under homeostatic and regenerative conditions.