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重复低剂量脂多糖转化的 C8-B4 小胶质细胞对链脲佐菌素诱导的 Neuro-2a 细胞死亡的预防作用。

Prevention of streptozotocin‑induced Neuro‑2a cell death by C8‑B4 microglia transformed with repetitive low‑dose lipopolysaccharide.

机构信息

Control of Innate Immunity, Collaborative Innovation Partnership, Takamatsu‑shi, Kagawa 761‑0301, Japan.

出版信息

Mol Med Rep. 2021 Oct;24(4). doi: 10.3892/mmr.2021.12328. Epub 2021 Jul 30.

Abstract

Diabetes‑associated neuronal dysfunction (DAND) is one of the serious complications of diabetes, but there is currently no remedy for it. Streptozotocin [2‑deoxy‑2‑(3‑methy1‑3‑nitrosoureido) D‑glucopyranose; STZ] is one of the most well‑established diabetes inducers and has been used and DAND models. The aim of the present study was to demonstrate that C8‑B4 microglia transformed by the stimulus of repetitive low‑dose lipopolysaccharide (LPSx3‑microglia) prevent STZ‑induced Neuro‑2a neuronal cell death . The ELISA results showed that neurotrophin‑4/5 (NT‑4/5) secretion was promoted in LPSx3‑microglia and the cell viability assay with trypan blue staining revealed that the culture supernatant of LPSx3‑microglia prevented STZ‑induced neuronal cell death. In addition, reverse transcription‑quantitative PCR showed that neurons treated with the culture supernatant of LPSx3‑microglia promoted the gene expression of B‑cell lymphoma‑extra large and glucose‑dependent insulinotropic polypeptide receptor. Furthermore, the inhibition of tyrosine kinase receptor B, a receptor of NT‑4/5, suppressed the neuroprotective effect of LPSx3‑microglia. Taken together, the present study demonstrated that LPSx3‑microglia prevent STZ‑induced neuronal death and that NT‑4/5 may be involved in the neuroprotective mechanism of LPSx3‑microglia.

摘要

糖尿病相关神经元功能障碍 (DAND) 是糖尿病的严重并发症之一,但目前尚无治愈方法。链脲佐菌素 [2-脱氧-2-(3-甲基-3-亚硝脲基) D-吡喃葡萄糖; STZ] 是最成熟的糖尿病诱导剂之一,已被用于和 DAND 模型。本研究旨在证明受重复低剂量脂多糖刺激的 C8-B4 小胶质细胞(LPSx3-小胶质细胞)可预防 STZ 诱导的 Neuro-2a 神经元细胞死亡。ELISA 结果显示 LPSx3-小胶质细胞中促进神经营养因子-4/5 (NT-4/5) 的分泌,台盼蓝染色细胞活力测定显示 LPSx3-小胶质细胞的培养上清液可预防 STZ 诱导的神经元细胞死亡。此外,逆转录-定量 PCR 显示神经元用 LPSx3-小胶质细胞的培养上清液处理后,B 细胞淋巴瘤-extra large 和葡萄糖依赖性胰岛素释放肽受体的基因表达增加。此外,酪氨酸激酶受体 B(NT-4/5 的受体)的抑制剂抑制了 LPSx3-小胶质细胞的神经保护作用。综上所述,本研究表明 LPSx3-小胶质细胞可预防 STZ 诱导的神经元死亡,NT-4/5 可能参与 LPSx3-小胶质细胞的神经保护机制。

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