Journal Article

Inhibition of P2X4R attenuates white matter injury in mice after intracerebral hemorrhage by regulating microglial phenotypes

Xu, Chaoran, Wu, Xinyan, Peng, Yucong, Zhou, Guoyang, Zhou, Hang, Li, Yin, Yan, Feng, Fu, Xiongjie, Zhuang, Jianfeng, Cao, Yang, Li, Jianru, Gao, Liansheng, Chen, Gao, Wang, Lin, Zeng, Hanhai

2021

Overview

Background White matter injury (WMI) is a major neuropathological event associated with intracerebral hemorrhage (ICH). P2X purinoreceptor 4 (P2X4R) is a member of the P2X purine receptor family, which plays a crucial role in regulating WMI and neuroinflammation in central nervous system (CNS) diseases. Our study investigated the role of P2X4R in the WMI and the inflammatory response in mice, as well as the possible mechanism of action after ICH. Methods ICH was induced in mice via collagenase injection. Mice were treated with 5-BDBD and ANA-12 to inhibit P2X4R and tropomyosin-related kinase receptor B (TrkB), respectively. Immunostaining and quantitative polymerase chain reaction (qPCR) were performed to detect microglial phenotypes after the inhibition of P2X4R. Western blots (WB) and immunostaining were used to examine WMI and the underlying molecular mechanisms. Cylinder, corner turn, wire hanging, and forelimb placement tests were conducted to evaluate neurobehavioral function. Results After ICH, the protein levels of P2X4R were upregulated, especially on day 7 after ICH, and were mainly located in the microglia. The inhibition of P2X4R via 5-BDBD promoted neurofunctional recovery after ICH as well as the transformation of the pro-inflammatory microglia induced by ICH into an anti-inflammatory phenotype, and attenuated ICH-induced WMI. Furthermore, we found that TrkB blockage can reverse the protective effects of WMI as well as neuroprotection after 5-BDBD treatment. This result indicates that P2X4R plays a crucial role in regulating WMI and neuroinflammation and that P2X4R inhibition may benefit patients with ICH. Conclusions Our results demonstrated that P2X4R contributes to WMI by polarizing microglia into a pro-inflammatory phenotype after ICH. Furthermore, the inhibition of P2X4R promoted pro-inflammatory microglia polarization into an anti-inflammatory phenotype, enhanced brain-derived neurotrophic factor (BDNF) production, and through the BDNF/TrkB pathway, attenuated WMI and improved neurological function. Therefore, the regulation of P2X4R activation may be beneficial for the reducing of ICH-induced brain injury.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Animals / BDNF / Benzodiazepinones - pharmacology / Biomedical and Life Sciences / Biomedicine / Brain / Brain injury / Brain-derived neurotrophic factor / Care and treatment / Cell receptors / Central nervous system / Cerebral Hemorrhage - metabolism / Cerebral Hemorrhage - pathology / Collagen / Collagenase / Complications and side effects / Development and progression / Disease Models, Animal / Experiments / Genotype & phenotype / Health aspects / Hemorrhage / Immunology / Inflammation / Injuries / Intracerebral hemorrhage / Laboratory animals / Male / Membrane Glycoproteins - metabolism / Mice / Microglia / Microglia - drug effects / Microglia - metabolism / Microglia - pathology / Microglia polarization / Molecular modelling / Motor Activity - drug effects / Neurobiology / Neurology / Neuroprotection / Neuroprotective Agents - pharmacology / Neurosciences / P2X4R / Phenotype / Phenotypes / Polymerase chain reaction / Protein-Tyrosine Kinases - metabolism / Proteins / Purine P2X receptors / Purinergic P2X Receptor Antagonists - pharmacology / Substantia alba / Traumatic brain injury / TrkB / TrkB receptors / Tropomyosin / Western blotting / White Matter - drug effects / White Matter - metabolism / White Matter - pathology / White matter injury