Caspase 3/ROCK1 pathway mediates high glucose-induced platelet microparticles shedding

• Published in: Biochemical and biophysical research communications 2019-02, Vol.509 (2), p.596-602
• Main Authors: Wang, Gui Hua, Ma, Kun Ling, Zhang, Yang, Hu, Ze Bo, Liu, Liang, Lu, Jian, Chen, Pei Pei, Lu, Chen Chen, Ruan, Xiong Zhong, Liu, Bi Cheng
• Format: Article
• Language: English
• Subjects: caspase3; High glucose; Platelet microparticles; Rho-associated kinase 1
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2018.12.166

Platelet microparticles (PMPs) are closely associated with diabetic macrovascular complications. This study aimed to explore the underlying mechanisms of high glucose-induced PMPs generation. Washed platelets, obtained from the plasma of healthy male Sprague-Dawley rats, were incubated with high glucose. PMPs were isolated using gradient centrifugation and counted by flow cytometry. Expression and activity of ROCK1 and caspase3 were evaluated by real-time PCR, Western blotting, and activity assay kit. High glucose enhanced PMPs shedding in the presence of collagen. The mRNA and protein levels of ROCK1, but not ROCK2, were increased in platelets incubated with high glucose. Y-27632, an inhibitor of ROCK, blocked the increased PMPs shedding induced by high glucose. Expression and activity of caspase3 were elevated in platelets under the high glucose conditions. Z-DVED-FMK, a caspase3 inhibitor, inhibited ROCK1 activity and decreased the PMPs generation under high glucose. High glucose increased PMPs shedding via caspase3-ROCK1 signal pathway. [Display omitted] •High glucose enhanced platelet microparticles shedding.•Caspase3 mediated activation of RCOK1 under high glucose.