| First Author | Sun X | Year | 2024 |
| Journal | Circ Res | Volume | 134 |
| Issue | 7 | Pages | 858-871 |
| PubMed ID | 38362769 | Mgi Jnum | J:371178 |
| Mgi Id | MGI:8160959 | Doi | 10.1161/CIRCRESAHA.123.323538 |
| Citation | Sun X, et al. (2024) Sorbs2 Deficiency and Vascular BK Channelopathy in Diabetes. Circ Res 134(7):858-871 |
| abstractText | BACKGROUND: Vascular large conductance Ca(2+)-activated K(+) (BK) channel, composed of the alpha-subunit (BK-alpha) and the beta1-subunit (BK-beta1), is a key determinant of coronary vasorelaxation and its function is impaired in diabetic vessels. However, our knowledge of diabetic BK channel dysregulation is incomplete. The Sorbs2 (Sorbin homology [SoHo] and Src homology 3 [SH3] domains-containing protein 2), is ubiquitously expressed in arteries, but its role in vascular pathophysiology is unknown. METHODS: The role of Sorbs2 in regulating vascular BK channel activity was determined using patch-clamp recordings, molecular biological techniques, and in silico analysis. RESULTS: Sorbs2 is not only a cytoskeletal protein but also an RNA-binding protein that binds to BK channel proteins and BK-alpha mRNA, regulating BK channel expression and function in coronary smooth muscle cells. Molecular biological studies reveal that the SH3 domain of Sorbs2 is necessary for Sorbs2 interaction with BK-alpha subunits, while both the SH3 and SoHo domains of Sorbs2 interact with BK-beta1 subunits. Deletion of the SH3 or SoHo domains abolishes the Sorbs2 effect on the BK-alpha/BK-beta1 channel current density. Additionally, Sorbs2 is a target gene of the Nrf2 (nuclear factor erythroid-2-related factor 2), which binds to the promoter of Sorbs2 and regulates Sorbs2 expression in coronary smooth muscle cells. In vivo studies demonstrate that Sorbs2 knockout mice at 4 months of age display a significant decrease in BK channel expression and function, accompanied by impaired BK channel Ca(2+)-sensitivity and BK channel-mediated vasodilation in coronary arteries, without altering their body weights and blood glucose levels. Importantly, Sorbs2 expression is significantly downregulated in the coronary arteries of db/db type 2 diabetic mice. CONCLUSIONS: Sorbs2, a downstream target of Nrf2, plays an important role in regulating BK channel expression and function in vascular smooth muscle cells. Vascular Sorbs2 is downregulated in diabetes. Genetic knockout of Sorbs2 manifests coronary BK channelopathy and vasculopathy observed in diabetic mice, independent of obesity and glucotoxicity. |
