2. Academic Validation
  3. Circular RNA PTP4A2 regulates microglial polarization through STAT3 to promote neuroinflammation in ischemic stroke

Circular RNA PTP4A2 regulates microglial polarization through STAT3 to promote neuroinflammation in ischemic stroke

  • CNS Neurosci Ther. 2023 Oct 23. doi: 10.1111/cns.14512.
Xingzhi Wang 1 2 3,  Shenyang Zhang 1 2,  Bingchen Lv 1 2,  Hao Chen 1 2,  Wei Zhang 1 2,  Liguo Dong 1 2,  Lei Bao 1 2,  Miao Wang 4,  Yan Wang 1 2,  Wenqi Mao 1 2,  Likun Cui 1 2,  Ye Pang 1 2,  Fei Wang 1 2,  Fuling Yan 5,  Zuohui Zhang 1 2,  Guiyun Cui 1 2
Affiliations

Affiliations

  • 1 Department of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
  • 2 Institute of Stroke Research, Xuzhou Medical University, Xuzhou, China.
  • 3 Jiangsu Key Laboratory of Brain Disease and Bioinformation, Research Center for Biochemistry and Molecular Biology, Xuzhou Medical University, Xuzhou, China.
  • 4 Department of Geriatrics, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
  • 5 Department of Neurology, Affiliated to ZhongDa Hospital of Southeast University, Nanjing, China.
PMID: 37869777 DOI: 10.1111/cns.14512
Abstract

Objective: Microglial polarization plays a critical role in neuroinflammation and may be a potential therapeutic target for ischemic stroke. This study was to explore the role and underlying molecular mechanism of Circular RNA PTP4A2 (circPTP4A2) in microglial polarization after ischemic stroke.

Methods: C57BL/6J mice underwent transient middle cerebral artery occlusion (tMCAO), while primary mouse microglia and BV2 microglial cells experienced oxygen glucose deprivation/reperfusion (OGD/R) to mimic ischemic conditions. CircPTP4A2 shRNA lentivirus and Colivelin were used to knock down circPTP4A2 and upregulate signal transducer and activator of transcription 3 (STAT3) phosphorylation, respectively. Microglial polarization was assessed using immunofluorescence staining and Western blot. RNA pull-down and RNA binding protein immunoprecipitation (RIP) were applied to detect the binding between circPTP4A2 and STAT3.

Results: The levels of circPTP4A2 were significantly increased in plasma and peri-infarct cortex in tMCAO mice. CircPTP4A2 knockdown reduced infarct volume, increased cortical cerebral blood flow (CBF), and attenuated neurological deficits. It also decreased pro-inflammatory factors levels in peri-infarct cortex and plasma, and increased anti-inflammatory factors concentrations 24 h post-stroke. In addition, circPTP4A2 knockdown suppressed M1 microglial polarization and promoted M2 microglial polarization in both tMCAO mice and OGD/R-induced BV2 microglial cells. Moreover, circPTP4A2 knockdown inhibited the phosphorylation of STAT3 induced by oxygen-glucose deprivation. In contrast, increased phosphorylation of STAT3 partly counteracted the effects of circPTP4A2 knockdown. RNA pull-down and RIP assays further certified the binding between circPTP4A2 and STAT3.

Conclusion: These results revealed regulatory mechanisms of circPTP4A2 that stimulated neuroinflammation by driving STAT3-dependent microglial polarization in ischemic brain injury. CircPTP4A2 knockdown reduced cerebral ischemic injury and promoted microglial M2 polarization, which could be a novel therapeutic target for ischemic stroke.

Keywords

STAT3; circPTP4A2; inflammation; ischemic stroke; microglia.

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