Premium
Upregulating the Expression of Survivin‐HBXIP Complex Contributes to the Protective Role of IMM‐H004 in Transient Global Cerebral Ischemia/Reperfusion
Author(s) -
Chu Shifeng,
Zhang Zhao,
Wang Zhenzhen
Publication year - 2018
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2018.32.1_supplement.824.7
Subject(s) - survivin , protein kinase b , apoptosis , foxo1 , phosphorylation , pi3k/akt/mtor pathway , ischemia , programmed cell death , cancer research , chemistry , medicine , microbiology and biotechnology , biology , biochemistry
IMM‐H004, a 3‐piperazinylcoumarin compound derived from coumarin, has been proved effective against CA1 cell loss and spatial learning impairments resulting from transient global ischemia/reperfusion (TGCI/R), while the mechanism is still largely unknown. Here, we confirmed that treatment of rats with IMM‐H004 immediately after TGCI/R ameliorated delayed neuronal death (DND) in the CA1 of hippocampus and cortex. Further study suggested that IMM‐H004 contributed to the expression of antiapoptotic protein survivin through the activation of PI3K‐dependent protein kinase B (PKB/Akt), which led to the phosphorylation of forkhead box O1 (FoxO1), then relieved the inhibiting effect on survivin promoter. Additionally, IMM‐H004 also enhanced the expression of hepatitis B X‐interacting protein (HBXIP), which formed a complex with survivin to prevent the activation of caspase death cascade, thereby halting apoptotic cell death. Finally, we injected a HBXIP siRNA into hippocampus and performed microelectroporation before ischemia/reperfusion, which abolished the protective effect of IMM‐H004. Further study revealed that HBXIP maintained the high expression of Akt and survivin. Collectively, our findings demonstrated that DND after TGCI/R was alleviated by IMM‐H004 through promoting the formation of survivin‐HBXIP complex, which further emphasized the importance of endogenous protein involved in self‐repair after stroke. Support or Funding Information This work was supported by the National Natural Science Foundation of China (81730096, U1402221), CAMS Innovation Fund for Medical Sciences (CIFMS) ( 2016‐I2M‐1‐004), the Scientific Research Foundation of the Higher Education Institutions of Hunan Province (15K091), Beijing Key Laboratory of New Drug Mechanisms and Pharmacological Evaluation Study (BZ0150), PUMC Graduate Education and Teaching Reform Project (10023201600801).Schematic diagram of the neural protective role of IMMH004 after TGCI/RThis abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .