Literature DB >> 29777731

Tumor necrosis factor receptor 2 is required for ischemic preconditioning-mediated neuroprotection in the hippocampus following a subsequent longer transient cerebral ischemia.

Jae-Chul Lee1, Chan Woo Park2, Myoung Cheol Shin2, Jun Hwi Cho2, Hyang-Ah Lee3, Young-Myeong Kim4, Joon Ha Park5, Ji Hyeon Ahn5, Jeong Hwi Cho6, Hyun-Jin Tae6, In Koo Hwang7, Tae-Kyeong Lee1, Moo-Ho Won8, Il Jun Kang9.   

Abstract

Tumor Necrosis Factor-α (TNF-α) is a proinflammatory cytokine implicated in neuronal damage in response to cerebral ischemia. Ischemic preconditioning (IPC) provides neuroprotection against a subsequent severer or longer transient ischemia by ischemic tolerance. Here, we focused on the role of TNF-α in IPC-mediated neuroprotection against neuronal death following a subsequent longer transient cerebral ischemia (TCI). Gerbils used in this study were randomly assigned to eight groups; sham group, TCI operated group, IPC plus (+) sham group, IPC + TCI operated group, sham + etanercept (an inhibitor of TNF-a) group, TCI + etanercept group, IPC + sham + etanercept group, and IPC + TCI + etanercept group. IPC was induced by a 2-min sublethal transient ischemia, which was operated 1 day prior to a longer (5-min) TCI. A significant death of neurons was found in the stratum pyramidale (SP) in the CA1 area (CA1) of the hippocampus 5 days after TCI; however, IPC protected SP neurons from TCI. We found that TNF-α immunoreactivity was significantly increased in CA1 pyramidal neurons in the TCI and IPC + TCI groups compared to the sham group. TNF-R1 expression in CA1 pyramidal neurons of the TCI group was also increased 1 and 2 days after TCI; however, in the IPC + TCI group, TNF-R1 expression was significantly lower than that in the TCI group. On the other hand, we did not detect TNF-R2 immunoreactivity in CA1 pyramidal neurons 1 and 2 days after TCI; meanwhile, in the IPC + TCI group, TNF-R2 expression was significantly increased compared to TNF-R2 expression at 1 and 2 days after TCI. In addition, in this group, TNF-R2 was newly expressed in pericytes, which are important cells in the blood brain barrier, from 1 day after TCI. When we treated etanercept to the IPC + TCI group, IPC-induced neuroprotection was significantly weakened. In brief, this study indicates that IPC confers neuroprotection against TCI by TNF-α signaling through TNF-R2 and suggests that the enhancement of TNF-R2 expression by IPC may be a legitimate strategy for a therapeutic intervention of TCI.
Copyright © 2018. Published by Elsevier Ltd.

Entities:  

Keywords:  Delayed neuronal death; Etanercept; Ischemia-reperfusion; Ischemic preconditioning; Tumor necrosis factor receptor; Tumor necrosis factor-α

Mesh:

Substances:

Year:  2018        PMID: 29777731     DOI: 10.1016/j.neuint.2018.05.008

Source DB:  PubMed          Journal:  Neurochem Int        ISSN: 0197-0186            Impact factor:   3.921


  2 in total

1.  Soluble tumor necrosis factor-alpha-induced hyperexcitability contributes to retinal ganglion cell apoptosis by enhancing Nav1.6 in experimental glaucoma.

Authors:  Shuo Cheng; Hong-Ning Wang; Lin-Jie Xu; Fang Li; Yanying Miao; Bo Lei; Xinghuai Sun; Zhongfeng Wang
Journal:  J Neuroinflammation       Date:  2021-08-21       Impact factor: 8.322

2.  Comparison of Neuronal Death, Blood-Brain Barrier Leakage and Inflammatory Cytokine Expression in the Hippocampal CA1 Region Following Mild and Severe Transient Forebrain Ischemia in Gerbils.

Authors:  Choong-Hyun Lee; Ji Hyeon Ahn; Tae-Kyeong Lee; Hyejin Sim; Jae-Chul Lee; Joon Ha Park; Myoung Cheol Shin; Jun Hwi Cho; Dae Won Kim; Moo-Ho Won; Soo Young Choi
Journal:  Neurochem Res       Date:  2021-05-29       Impact factor: 3.996

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.