Journal
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
Volume 37, Issue 3, Pages 890-901Publisher
SAGE PUBLICATIONS INC
DOI: 10.1177/0271678X16647398
Keywords
cortical spreading depression; microglia; high-mobility group box I; Toll-like receptors; cathepsin D
Categories
Funding
- JSPS KAKENHI [26460706, 22390132]
- Takeda Science Foundation
- Pfizer Inc. [WS1878886]
- Keio University Doctorate Student
- Grants-in-Aid for Scientific Research [26460706, 22390132, 26350981] Funding Source: KAKEN
Ask authors/readers for more resources
Single episodes of cortical spreading depression (CSD) are believed to cause typical migraine aura, whereas clusters of spreading depolarizations have been observed in cerebral ischemia and subarachnoid hemorrhage. We recently demonstrated that the release of high-mobility group box I (HMGBI) from cortical neurons after CSD in a rodent model is dependent on the number of CSD episodes, such that only multiple CSD episodes can induce significant HMGBI release. Here, we report that only multiple CSD inductions caused microglial hypertrophy (activation) accompanied by a greater impact on the transcription activity of the HMGBI receptor genes, TLR2 and TLR4, while the total number of cortical microglia was not affected. Both an HMGBI-neurtalizing antibody and the HMGBI inhibitor glycyrrhizin abrogated multiple CSD-induced microglial hypertrophy. Moreover, multiple CSD inductions failed to induce microglial hypertrophy in TLR2/4 double knockout mice. These results strongly implicate the HMGBI-TLR2/4 axis in the activation of microglia following multiple CSD inductions. Increased expression of the lysosomal acid hydrolase cathepsin D was detected in activated microglia by immunostaining, suggesting that lysosomal phagocytic activity may be enhanced in multiple CSD-activated microglia.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available