Institute for Biomedical Sciences of Pain, Tangdu Hospital, The Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.
Int J Mol Med. 2013 Nov;32(5):1021-8. doi: 10.3892/ijmm.2013.1486. Epub 2013 Sep 11.
It has been shown that aging can greatly influence the integrity and ultrastructure of white matter and the myelin sheath; however, studies regarding the effects of aging on the expression of myelin proteins are still limited. In the present study, immunohistochemical mapping was used to investigate the overall expression of myelin basic protein (Mbp) and myelin oligodendrocyte glycoprotein (Mog) in the central nervous system (CNS) of rats in postnatal months 2, 5, 18 and 26. Astrocyte and microglia activation was also detected by glial fibrillary acidic protein (GFAP) or ionized calcium-binding adaptor molecule 1 (Iba1) staining and western blotting. A significant decline of Mbp and Mog was identified as a universal alteration in the CNS of aged rats. Aging also induced significant astrocyte and microglial activation. Correlation analysis indicated a negative correlation between the reduction of age‑related myelin proteins and glial activation in aging. This correlation of myelin breakdown and glial activation in aging may reveal new evidence in connecting the inflammation and myelin breakdown mechanism of age‑related neurodegenerative diseases.
研究表明,衰老会极大地影响白质和髓鞘的完整性和超微结构;然而,关于衰老对髓鞘蛋白表达影响的研究仍然有限。在本研究中,通过免疫组织化学图谱分析,研究了髓鞘碱性蛋白(Mbp)和少突胶质细胞糖蛋白(Mog)在出生后 2、5、18 和 26 月龄大鼠中枢神经系统(CNS)中的整体表达。通过胶质纤维酸性蛋白(GFAP)或钙结合衔接分子 1(Iba1)染色和 Western blot 检测星形胶质细胞和小胶质细胞的激活。研究结果表明,Mbp 和 Mog 的显著下降是衰老大鼠中枢神经系统的普遍改变。衰老还诱导了明显的星形胶质细胞和小胶质细胞激活。相关性分析表明,与年龄相关的髓鞘蛋白减少与衰老过程中的神经胶质激活呈负相关。这种衰老过程中髓鞘破坏与神经胶质激活的相关性可能为连接年龄相关性神经退行性疾病的炎症和髓鞘破坏机制提供新的证据。