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在共培养条件下,新生大鼠背根神经节卫星胶质细胞中 P2X7R 的下调导致神经元 TRPV1 表达减少。

Reduction of TRPV1 expression on neurons due to downregulation of P2X7R in neonatal rat dorsal root ganglion satellite glial cells under co-culture conditions.

机构信息

Department of Physiology, Basic Medical College of Nanchang University, Nanchang, P.R. China.

College of Economics and Management, Shanghai Ocean University, Shanghai, P.R. China.

出版信息

Biol Cell. 2024 Oct;116(10):e2400021. doi: 10.1111/boc.202400021. Epub 2024 Aug 19.

Abstract

BACKGROUND INFORMATION

The purinergic ligand-gated ion channel 7 receptor (P2X7R) is an ATP-gated ion channel that transmits extracellular signals and induces corresponding biological effects, transient receptor potential vanilloid type 1 (TRPV1) is a non-selective cation channel that maintains normal physiological functions; numerous studies showed that P2X7R and TRPV1 are associated with inflammatory reactions.

RESULTS

The effect of P2X7R knockdown in satellite glial cells (SGCs) on neuronal TRPV1 expression under high glucose and high free fat (HGHF) environment was investigated. P2X7 short hairpin RNA (shRNA) was utilized to downregulate P2X7R in SGCs, and treated and untreated SGCs were co-cultured with neuronal cell lines. The expression levels of inflammatory factors and signaling pathways in SGCs and neurons were measured using Western blot analysis, RT-qPCR, immunofluorescence, and enzyme-linked immunosorbent assays. Results suggested that P2X7 shRNA reduced the expression levels of P2X7R protein and mRNA in SGCs surrounding DRG neurons and downregulated the release of tumor necrosis factor-alpha and interleukin-1 beta via the Ca/p38 MAPK/NF-κB pathway. Additionally, the downregulation of P2X7R might decrease TRPV1 expression in neurons via the Ca/PKC-ɛ/p38 MAPK pathway.

CONCLUSIONS

Reducing P2X7R expression in SCGs in an HGHF environment could decrease neuronal TRPV1 expression via the Ca/PKC-ɛ/p38 MAPK pathway.

摘要

背景信息

嘌呤能配体门控离子通道 7 受体(P2X7R)是一种 ATP 门控离子通道,可传递细胞外信号并诱导相应的生物学效应;瞬时受体电位香草酸 1 型(TRPV1)是非选择性阳离子通道,维持正常的生理功能;大量研究表明,P2X7R 和 TRPV1 与炎症反应有关。

结果

研究了高糖和高游离脂肪酸(HGHF)环境下卫星胶质细胞(SGC)中 P2X7R 敲低对神经元 TRPV1 表达的影响。利用 P2X7 短发夹 RNA(shRNA)下调 SGC 中的 P2X7R,并将处理和未处理的 SGC 与神经元细胞系共培养。采用 Western blot 分析、RT-qPCR、免疫荧光和酶联免疫吸附试验测定 SGC 和神经元中炎症因子和信号通路的表达水平。结果表明,P2X7 shRNA 降低了 DRG 神经元周围 SGC 中 P2X7R 蛋白和 mRNA 的表达水平,并通过 Ca/p38 MAPK/NF-κB 通路下调肿瘤坏死因子-α和白细胞介素-1β的释放。此外,通过 Ca/PKC-ɛ/p38 MAPK 通路,P2X7R 的下调可能降低神经元中 TRPV1 的表达。

结论

在 HGHF 环境下降低 SGC 中的 P2X7R 表达可能通过 Ca/PKC-ɛ/p38 MAPK 通路降低神经元 TRPV1 的表达。

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