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. 2025 Jun 4.
doi: 10.1007/s12035-025-05080-4. Online ahead of print.

LncRNA ZFAS1 Combined with SRSF1 Regulate CNPY2 Expression and Leads to Microglia Endoplasmic Reticulum Stress-Induced Spinal Cord Injury

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LncRNA ZFAS1 Combined with SRSF1 Regulate CNPY2 Expression and Leads to Microglia Endoplasmic Reticulum Stress-Induced Spinal Cord Injury

Pengcheng Chen et al. Mol Neurobiol. .

Abstract

Spinal cord injury (SCI) has a high mortality and disability rate. Endoplasmic reticulum (ER) stress induces neuronal apoptosis and participates in the regulation of SCI. LncRNA ZFAS1 can participate in the regulation of SCI by influencing ER stress; however, its mechanism is worth further exploring. The molecular mechanism of lncRNA ZFAS1 regulating spinal cord injury was evaluated by in vitro and in vivo experiments. We established an SCI model in vitro by inducing mouse microglia (BV-2) with LPS. The regulation of SCI was verified by transfection of shRNA knockdown lncRNA ZFAS1 and CNPY2. The expression levels of related genes and proteins were detected by qPCR and western blot. The proportion of apoptosis was analyzed by flow cytometry and TUNEL staining. RIP and RNA pull down verified that lncRNA ZFAS1 combined with SRSF1 stabilized CNPY2 mRNA. It was verified that lncRNA ZFAS1 promoted ER stress and accelerated SCI injury in SCI mice model. Our results showed that the expression of lncRNA ZFAS1 and CNPY2 increased in SCI cell model, which was related to SCI injury. Knocking down lncRNA ZFAS1 or CNPY2 could inhibit ER stress and reduce apoptosis of BV-2 cells. Inhibition of lncRNA ZFAS1 in SCI mice increased the number of spinal cord neurons and ER stress response, and improved SCI injury in mice. Molecular experiments confirmed that lncRNA ZFAS1 stabilized CNPY2 mRNA by binding to SRSF1. And the lncRNA ZFAS1/CNPY2 axis was involved in regulating ER stress and apoptosis of BV-2 cells. LncRNA ZFAS1 stabilized CNPY2 by combining with SRSF1, which led to ER stress in microglia and promoted SCI. LncRNA ZFAS1 may be a potential target gene for the prevention and treatment of SCI.

Keywords: CNPY2; Endoplasmic reticulum stress; LncRNA ZFAS1; Spinal cord injury.

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Conflict of interest statement

Declarations. Ethics Approval and Consent to Participate: All animal experiments were conducted in accordance with the guidelines approved by the Haikou Affiliated Hospital of Central South University Xiangya School of Medicine Ethics Committee (No. 2024-(LS)-194). Consent for Publication: Not applicable. Declaration of Generative AI and AI-Assisted Technologies in the Writing Process: During the preparation of this work, the authors did not use any AI-assisted technology. Conflict of interest: The authors declare no competing interests.

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References

    1. Kim HN, McCrea MR, Li S (2023) Advances in molecular therapies for targeting pathophysiology in spinal cord injury. Expert Opin Ther Targets 27(3):171–187. https://doi.org/10.1080/14728222.2023.2194532 - DOI - PubMed - PMC
    1. Yu M, Wang Z, Wang D, Aierxi M, Ma Z, Wang Y (2023) Oxidative stress following spinal cord injury: from molecular mechanisms to therapeutic targets. J Neurosci Res 101(10):1538–1554. https://doi.org/10.1002/jnr.25221 - DOI - PubMed
    1. Liu Z, Yao X, Jiang W, Li W, Zhu S, Liao C, Zou L, Ding R et al (2020) Advanced oxidation protein products induce microglia-mediated neuroinflammation via MAPKs-NF-kappaB signaling pathway and pyroptosis after secondary spinal cord injury. J Neuroinflammation 17(1):90. https://doi.org/10.1186/s12974-020-01751-2 - DOI - PubMed - PMC
    1. Tran AP, Warren PM, Silver J (2018) The biology of regeneration failure and success after spinal cord injury. Physiol Rev 98(2):881–917. https://doi.org/10.1152/physrev.00017.2017 - DOI - PubMed - PMC
    1. Lu E, Tang Y, Chen J, Al Mamun A, Feng Z, Cao L, Zhang X, Zhu Y et al (2023) Stub1 ameliorates ER stress-induced neural cell apoptosis and promotes locomotor recovery through restoring autophagy flux after spinal cord injury. Exp Neurol 368:114495. https://doi.org/10.1016/j.expneurol.2023.114495 - DOI - PubMed

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