Nadon N L, Duncan I D
Biology Dept, University of Tulsa, OK 74104, USA.
J Neurosci Res. 1995 May 1;41(1):96-104. doi: 10.1002/jnr.490410111.
The proteolipid proteins play a major role in the structure of the CNS myelin sheath, but they have also been implicated in the oligodendrocyte development leading to myelination. Mutations in the PLP gene result in severe dysmyelination and a paucity of mature oligodendrocytes. The myelin deficient (md) rat, carrying a Thr75-->Pro substitution present in both isoforms of proteolipid protein (PLP and DM20), is the most severely affected of the PLP mutants described to date. The expression of myelin associated genes was quantitated to determine the effect of the mutation on oligodendrocyte development in vivo. At 5 days postnatal, gene expression in the md rat approximated that in age-matched control rats, but as they matured, there was a progressive inhibition of gene expression in the md rats. The genes expressed late in the myelination program (PLP and MBP) were affected more dramatically than those expressed earlier in oligodendrocyte development (CNP and GPDH). The results indicate that the later stages of oligodendrocyte maturation and myelin elaboration are inhibited.
蛋白脂质蛋白在中枢神经系统髓鞘结构中起主要作用,但它们也与导致髓鞘形成的少突胶质细胞发育有关。PLP基因的突变会导致严重的髓鞘形成障碍和成熟少突胶质细胞数量减少。髓磷脂缺陷(md)大鼠携带蛋白脂质蛋白(PLP和DM20)两种同工型中均存在的Thr75→Pro替换,是迄今为止描述的PLP突变体中受影响最严重的。对髓鞘相关基因的表达进行定量分析,以确定该突变对体内少突胶质细胞发育的影响。出生后5天,md大鼠的基因表达与年龄匹配的对照大鼠相近,但随着它们的成熟,md大鼠的基因表达受到逐渐抑制。在髓鞘形成程序后期表达的基因(PLP和MBP)比在少突胶质细胞发育早期表达的基因(CNP和GPDH)受到的影响更大。结果表明,少突胶质细胞成熟和髓鞘形成的后期阶段受到抑制。