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Publication : Activation of Sigma-1 Receptor Enhanced Pericyte Survival via the Interplay Between Apoptosis and Autophagy: Implications for Blood-Brain Barrier Integrity in Stroke.

First Author  Zhang Y Year  2020
Journal  Transl Stroke Res Volume  11
Issue  2 Pages  267-287
PubMed ID  31290080 Mgi Jnum  J:310492
Mgi Id  MGI:6762741 Doi  10.1007/s12975-019-00711-0
Citation  Zhang Y, et al. (2020) Activation of Sigma-1 Receptor Enhanced Pericyte Survival via the Interplay Between Apoptosis and Autophagy: Implications for Blood-Brain Barrier Integrity in Stroke. Transl Stroke Res 11(2):267-287
abstractText  Stroke is a cerebrovascular disorder that affects many people worldwide. Pericytes play an important role in stroke progression and recovery. The sigma-1 receptor (sigma-1R) signaling pathway has been suggested as having promising neuroprotective potential in treating stroke; however, whether sigma-1R activation regulates pericyte function remains unknown. The aim of this study was to elucidate the role of sigma-1R and a novel sigma-1R agonist in pericytes following ischemic stroke. An ischemic stroke animal model was induced by photothrombotic middle cerebral artery occlusion (pMCAO) in sigma-1R knockout (KO) and wild-type (WT) mice. After pMCAO, there was significant pericyte loss and coverage in sigma-1R KO mice compared with WT mice as determined using transmission electron microscopy, immunofluorescence staining, and western blot. Interestingly, a novel sigma-1R agonist decreased infarct volume and blood-brain barrier damage with a concomitant amelioration of pericyte loss, as determined by western blot. Further studies indicated that cell apoptosis and autophagy were induced in an in vivo pMCAO ischemic stroke animal model and an in vitro oxygen glucose deprivation-treatment group. Inhibition of autophagy using a pharmacological approach significantly mitigated pericyte apoptosis, suggesting that autophagy was upstream of apoptosis in pericytes. Both in vivo and in vitro studies indicated that the sigma-1R agonist significantly decreased cell apoptosis via inhibition of autophagy with a subsequent enhancement of pericyte survival. This study identified the unique roles for sigma-1R in mediating pericyte survival via the regulation of the interplay between apoptosis and autophagy, suggesting that a novel sigma-1R agonist may be a promising therapeutic agent for the treatment of stroke patients.
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