α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation

Elevated inflammatory reactions are a significant component in cerebral ischemia–reperfusion injury (CIRI). Activation of α7-Nicotinic Acetylcholine Receptor (α7nAChR) reduces stroke-induced inflammation in rats, but the anti-inflammatory pathway in microglia under CIRI condition remains unclear. Th...

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Main Authors: Hasan, Mohammad Yusuf, Md Roslan, Azim Haikal, Azmi, Norazrina, Mohamed Ibrahim, Norlinah, Arulsamy, Alina, Lee, Vanessa Lin Lin, Siran, Rosfaiizah, Vidyadaran, Sharmili
Format: Article
Language:English
Published: Springer 2024
Online Access:http://psasir.upm.edu.my/id/eprint/118659/
http://psasir.upm.edu.my/id/eprint/118659/1/118659.pdf
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author Hasan, Mohammad Yusuf
Md Roslan, Azim Haikal
Azmi, Norazrina
Mohamed Ibrahim, Norlinah
Arulsamy, Alina
Lee, Vanessa Lin Lin
Siran, Rosfaiizah
Vidyadaran, Sharmili
author_facet Hasan, Mohammad Yusuf
Md Roslan, Azim Haikal
Azmi, Norazrina
Mohamed Ibrahim, Norlinah
Arulsamy, Alina
Lee, Vanessa Lin Lin
Siran, Rosfaiizah
Vidyadaran, Sharmili
author_sort Hasan, Mohammad Yusuf
building UPM Institutional Repository
collection Online Access
description Elevated inflammatory reactions are a significant component in cerebral ischemia–reperfusion injury (CIRI). Activation of α7-Nicotinic Acetylcholine Receptor (α7nAChR) reduces stroke-induced inflammation in rats, but the anti-inflammatory pathway in microglia under CIRI condition remains unclear. This study employed qRT-PCR, protein assays, NanoString analysis, and bioinformatics to examine the effects of PNU282987 treatment (α7nAChR agonist) on BV2 microglial functional differentiation in oxygen–glucose deprivation/reoxygenation (OGDR) condition. OGDR significantly increased the gene expression of pro-inflammatory markers such as TNF-α, IL-6, and IL1β, while α7nAChR agonists reduced these markers. The anti-inflammatory gene marker IL-10 was upregulated by α7nAChR agonist treatment. Downstream pathway marker analysis showed that both gene and protein expression of NFκB was associated with anti-inflammatory effects. Blocking microRNA-21 with antagomir reversed the anti-inflammatory effects. NanoString analysis revealed that microRNA-21 inhibition significantly affected inflammation-related genes, including AL1RAP, TLR9, FLT1, PTGIR, NFκB, TREM2, TNF, SMAD7, FOS, CCL5, IFIT1, CFB, CXCL10, IFI44, DDIT3, IRF7, OASL1, IL1A, IFIT2, C3, CD40, STAT2, IFIT3, IL1RN, OAS1A, CSF1, CCL4, CCL2, CCL3, BCL2L1, and ITGB2. Enrichment analysis of upregulated genes identified Gene Ontology Biological Processes related to cytokine responses and TNF-associated pathways. This study highlights α7nAChR activation as a key regulator of anti-inflammatory responses in BV2 microglia under OGDR conditions, with micro-RNA21 identified as a crucial mediator of receptor-driven neuroprotection via the TNF-α/NFκB signalling pathway.
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institution Universiti Putra Malaysia
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language English
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recordtype eprints
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spelling upm-1186592025-07-21T07:09:34Z http://psasir.upm.edu.my/id/eprint/118659/ α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation Hasan, Mohammad Yusuf Md Roslan, Azim Haikal Azmi, Norazrina Mohamed Ibrahim, Norlinah Arulsamy, Alina Lee, Vanessa Lin Lin Siran, Rosfaiizah Vidyadaran, Sharmili Elevated inflammatory reactions are a significant component in cerebral ischemia–reperfusion injury (CIRI). Activation of α7-Nicotinic Acetylcholine Receptor (α7nAChR) reduces stroke-induced inflammation in rats, but the anti-inflammatory pathway in microglia under CIRI condition remains unclear. This study employed qRT-PCR, protein assays, NanoString analysis, and bioinformatics to examine the effects of PNU282987 treatment (α7nAChR agonist) on BV2 microglial functional differentiation in oxygen–glucose deprivation/reoxygenation (OGDR) condition. OGDR significantly increased the gene expression of pro-inflammatory markers such as TNF-α, IL-6, and IL1β, while α7nAChR agonists reduced these markers. The anti-inflammatory gene marker IL-10 was upregulated by α7nAChR agonist treatment. Downstream pathway marker analysis showed that both gene and protein expression of NFκB was associated with anti-inflammatory effects. Blocking microRNA-21 with antagomir reversed the anti-inflammatory effects. NanoString analysis revealed that microRNA-21 inhibition significantly affected inflammation-related genes, including AL1RAP, TLR9, FLT1, PTGIR, NFκB, TREM2, TNF, SMAD7, FOS, CCL5, IFIT1, CFB, CXCL10, IFI44, DDIT3, IRF7, OASL1, IL1A, IFIT2, C3, CD40, STAT2, IFIT3, IL1RN, OAS1A, CSF1, CCL4, CCL2, CCL3, BCL2L1, and ITGB2. Enrichment analysis of upregulated genes identified Gene Ontology Biological Processes related to cytokine responses and TNF-associated pathways. This study highlights α7nAChR activation as a key regulator of anti-inflammatory responses in BV2 microglia under OGDR conditions, with micro-RNA21 identified as a crucial mediator of receptor-driven neuroprotection via the TNF-α/NFκB signalling pathway. Springer 2024-12-24 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/118659/1/118659.pdf Hasan, Mohammad Yusuf and Md Roslan, Azim Haikal and Azmi, Norazrina and Mohamed Ibrahim, Norlinah and Arulsamy, Alina and Lee, Vanessa Lin Lin and Siran, Rosfaiizah and Vidyadaran, Sharmili (2024) α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation. Journal of Molecular Neuroscience, 75 (2). pp. 1-13. ISSN 0895-8696; eISSN: 1559-1166 https://link.springer.com/article/10.1007/s12031-024-02300-9?error=cookies_not_supported&code=d726203b-3768-48f7-bd4a-defa15d6fac9 10.1007/s12031-024-02300-9
spellingShingle Hasan, Mohammad Yusuf
Md Roslan, Azim Haikal
Azmi, Norazrina
Mohamed Ibrahim, Norlinah
Arulsamy, Alina
Lee, Vanessa Lin Lin
Siran, Rosfaiizah
Vidyadaran, Sharmili
α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title_full α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title_fullStr α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title_full_unstemmed α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title_short α7-Nicotinic Acetylcholine Receptor activation modulates BV2 microglial plasticity via miR-21/TNF-α/NFκB in oxygen–glucose deprivation/reoxygenation
title_sort α7-nicotinic acetylcholine receptor activation modulates bv2 microglial plasticity via mir-21/tnf-α/nfκb in oxygen–glucose deprivation/reoxygenation
url http://psasir.upm.edu.my/id/eprint/118659/
http://psasir.upm.edu.my/id/eprint/118659/
http://psasir.upm.edu.my/id/eprint/118659/
http://psasir.upm.edu.my/id/eprint/118659/1/118659.pdf