LAUSR

Abstract Human embryonic stem cells (hESCs) are highly fragile with massive cell death after dissociation into single cells, which seriously hampers their applications. The mechanism underlying the massive cell death after dissociation still remains elusive. Here, the expression of apoptosis‐related proteins, cell survival and mitochondrial membrane potential in dissociated hESCs before and after the treatments with a protein kinase A (PKA) inhibitor H89 and p53 inhibitor Pifithrin &agr; were investigated, respectively. Protein interactions were identified by immunoprecipitation and immunofluorescence. The results show that the dissociation causes Caspase‐dependent apoptosis in hESCs mediated by mitochondrial pathway with the up‐regulation of pro‐apoptotic proteins, decrease in mitochondrial membrane potential and elevation in pro‐apoptotic Cyto c release, which are obviously suppresses by H89. The dissociation‐induced increase of phosphorylated p53 Ser15 (p‐p53) is suppressed by Pifithrin &agr; which also rescues the elevated levels of pro‐apoptotic proteins in mitochondrial pathway. During the dissociation‐induced apoptosis, PKA/p‐p53/Bax signaling pathway is identified by immunoprecipitation and immunofluorescence showing the most likely interaction between them. These results indicate that dissociation induces mitochondrial apoptosis in hESCs involving PKA/p‐p53/Bax signaling pathway, which not only give new insights into the apoptosis mechanism of dissociated hESCs, but also provide clues for developing potential strategies to promote hESC survival after dissociation. HighlightshESC dissociation causes mitochondrial apoptosis.H89 and Pifithrin &agr; suppress dissociation‐induced mitochondrial apoptosis.PKA/p‐p53/Bax signaling pathway is involved in dissociation‐induced hESC apoptosis.