Pin1 in cardiovascular dysfunction: A potential double-edge role

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• 作者：Jing-Zhang Wang ; ^{wangjingzhang1981@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; ^{jingzhangwang@hebeu.edu.cn" class="auth_mail" title="E-mail the corresponding author} ; Gui-Jing Liu ; Zhi-Ying Li ; Xiao-Hua Wang
• 关键词：NO ; nitric oxide ; eNOS ; endothelial nitric oxide synthase ; iNOS ; inducible nitric oxide synthase ; BAEC ; bovine aortic endothelial cell ; HAEC ; human aortic endothelial cell ; MPC ; mouse primary cardiomyocyte ; RAEC ; rat aortic endothelial cell ; VEGF ; vascular endothelial growth factor ; PDLC ; human periodontal ligament cell ; PCHC ; primary cultured human chondrocyte ; MAEC ; murine aortic endothelial cell ; Aβ ; amyloid-β
• 刊名：International Journal of Cardiology
• 出版年：2016
• 出版时间：1 June 2016
• 年：2016
• 卷：212
• 期：Complete
• 页码：280-283
• 全文大小：404 K

文摘

Our lab focused on the structural and functional properties of Pin1, which is the only known cis–trans isomerase regulating pSer/pThr–Pro motifs in proteins and facilitates various signaling pathways. We are lucky enough to read the article, contributed by Costantino et al. in your esteemed journal, on the role of Pin1 in diabetes-induced vascular dysfunction. Pin1 regulates the production of nitric oxide (NO), which is a key physiological stimulator of blood vessels and promotes vascular relaxation responses significantly. However, the regulation of cardiovascular diseases by Pin1 is somewhat controversial.

Methods and results

We compared the recent studies that support the down-regulation, as well as up-regulation, of NO production by Pin1 and tried to explore the underlying molecular mechanisms. We especially compared the different regulations of endothelial nitric oxide synthase (eNOS) and inducible nitric oxide synthase (iNOS) by Pin1, which is potentially the major reason leading to the controversial role of Pin1. Interestingly, the regulation of both eNOS and iNOS by Pin1 involves a double-edge effect, positively and negatively, contributing to paradoxical Pin1 functions in different animal models and cell lines. The extremely complex Pin1-regulated signaling networks might further exacerbate distinct cellular responses in vivo and influence NO production.

Conclusions

Pin1 plays a dual role, both positive and negative, in regulating NO production and in mediating the pathogenesis of cardiovascular diseases. Pin1 functions may vary a lot under different circumstances. Future investigations should focus on eNOS as well as iNOS in order to increase authenticity and accuracy of results.