Genome-Wide Screen and Validation of Microglia Pro-Inflammatory Mediators in Stroke
Authors:
Open Access
- 1 January 2021
- journal article
- research article
- Published by Aging and Disease in Aging and disease
- Vol. 12 (3) , 786-800
Abstract
Stroke activates microglia pro-inflammatory response that not only induces the early neuronal injuries but also causes the secondary brain infarction. Yet, the underlying mechanisms for how microglia become activated in stroke are still unknown. Here, using the next-generation of RNA sequencing we find a total of 778 genes increasingly expressed in brain of stroke mice. Of these, we identified Hmgb2 as a microglia pro-inflammatory mediator by promoting the transcription of Ctss. Inhibition of either Hmgb2 or Ctss blocks microglia pro-inflammatory response and protects against brain damages and improves the neurological functions of stroke mice. This study uncovers Hmgb2 and Ctss as the major microglia inflammatory response mediators in stroke and hence warrants the promising targets for stroke therapies.Keywords
This publication has 22 references indexed in Scilit:
- Stroke in China: advances and challenges in epidemiology, prevention, and managementThe Lancet Neurology, 2019
- Innate immune memory in the brain shapes neurological disease hallmarksNature, 2018
- Global Burden of StrokeSeminars in Neurology, 2018
- A small molecule binding HMGB1 and HMGB2 inhibits microglia-mediated neuroinflammationNature Chemical Biology, 2014
- Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic FactorCell, 2013
- Microglia/Macrophage Polarization Dynamics Reveal Novel Mechanism of Injury Expansion After Focal Cerebral IschemiaStroke, 2012
- The immunology of stroke: from mechanisms to translationNature Medicine, 2011
- DAPK1 Interaction with NMDA Receptor NR2B Subunits Mediates Brain Damage in StrokeCell, 2010
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression dataBioinformatics, 2009
- Neuronal Basic Helix-Loop-Helix Proteins (NEX, neuroD, NDRF): Spatiotemporal Expression and Targeted Disruption of the NEX Gene in Transgenic MiceJournal of Neuroscience, 1998