Department of Life Sciences, College of Biosciences and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
Department of Biotechnology and Bioindustry Sciences, College of Biosciences and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
Mol Neurobiol. 2024 Apr;61(4):1953-1968. doi: 10.1007/s12035-023-03681-5. Epub 2023 Oct 11.
Oligodendrocytes (OLs) form myelin sheaths around axons in the central nervous system (CNS) facilitate the propagation of action potentials. The studies have shown that the differentiation and maturation of OLs involve microRNA (miR) regulation. The recent findings have addressed that miR-204 regulates OL differentiation in culture. In this study, through in situ hybridization in combination with immunohistochemistry, we showed that microRNA-204-5p in the corpus callosum was mainly expressed in OLs immunoreactive with adenomatous polyposis coli (APC), an OL marker. We also found miR-204-5p expression in mature OLs was suppressed by the addition of interleukin-6 (IL-6). Moreover, IL-6-induced inhibition of miR-204-5p expression was blocked by the addition of the inhibitors specific for p38 mitogen-activated protein kinase (p38MAPK) or phosphatidylinositol 3-kinase (PI3K) pathway. We further utilized a rat model by feeding cuprizone (CPZ)-containing diet for 3 weeks to induce demyelination and gliosis in the corpus callosum, as well as the upregulation of IL-6 gene expression significantly. Despite that miR-204-5p expression in the corpus callosum was not altered after feeding by CPZ for 3 weeks, its expression was increased and IL-6 transcription was decreased in the corpus callosum of the recovery group that was fed by CPZ for the first 2 weeks and by the regular diet for one more week. Our data demonstrate that miR-204-5p expression in OLs declined under the influence of the inflamed microenvironment. The findings that an increase in miR-204-5p and declined IL-6 expression observed in the recovery group might be involved with OL repair in the corpus callosum, and also shed light on a potential role for miR-204-5p in OL homeostasis following the white matter injury.
少突胶质细胞(OLs)在中枢神经系统(CNS)中形成轴突的髓鞘,促进动作电位的传播。研究表明,OL 的分化和成熟涉及 microRNA(miR)调节。最近的研究表明,miR-204 在培养物中调节 OL 的分化。在这项研究中,我们通过原位杂交结合免疫组织化学,显示了胼胝体中的 microRNA-204-5p 主要在 OL 标志物 APC 阳性的 OL 中表达。我们还发现,IL-6 的添加抑制了成熟 OL 中 miR-204-5p 的表达。此外,添加特异性针对 p38 丝裂原活化蛋白激酶(p38MAPK)或磷脂酰肌醇 3-激酶(PI3K)途径的抑制剂可阻断 IL-6 诱导的 miR-204-5p 表达抑制。我们进一步利用大鼠模型,通过喂食含杯状病毒(CPZ)的饮食 3 周,诱导胼胝体脱髓鞘和神经胶质增生,以及 IL-6 基因表达显著上调。尽管在 CPZ 喂养 3 周后,胼胝体中的 miR-204-5p 表达没有改变,但在 CPZ 喂养前 2 周和再喂养 1 周的恢复组中,其表达增加,IL-6 转录减少。我们的数据表明,在炎症微环境的影响下,OL 中的 miR-204-5p 表达下降。在恢复组中观察到 miR-204-5p 增加和 IL-6 表达下降,这可能与胼胝体中的 OL 修复有关,也为 miR-204-5p 在白质损伤后 OL 稳态中的潜在作用提供了线索。