伊诺斯
内皮型一氧化氮合酶
蛋白质酪氨酸磷酸酶
一氧化氮
一氧化氮合酶
一氧化氮合酶Ⅲ型
糖尿病
内科学
内分泌学
内皮
磷酸酶
2型糖尿病
医学
化学
受体
细胞生物学
生物
生物化学
酶
作者
Alberto Fernando Oliveira Justo,Pedro Paulo Luciano Afonso
标识
DOI:10.1007/s12079-021-00611-9
摘要
Endothelial nitric oxide synthase (eNOS) and receptor-type vascular endothelial protein tyrosine phosphatase (VE-PTP) are one of the majors signaling pathways related to endothelial health in diabetes. Several reports have shown that the inhibition of VE-PTP can lead the nitric oxide production, although repeated studies showed that VE-PTP regulated the eNOS exclusive at Ser1177 in indirect-manner. A recent, exciting paper (Siragusa et al. in Cardiovasc Res, 2020. https://doi.org/10.1093/cvr/cvaa213 ), showing that VE-PTP regulates eNOS in a direct-manner, dephosphorylating eNOS at Tyr81 and indirect at Ser1177 and the effects of a VE-PTP inhibitor, AKB-9778, in the blood pressure from diabetic patients.
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