Jiang Shuxian, Seng Seyha, Avraham Hava Karsenty, Fu Yigong, Avraham Shalom
Division of Experimental Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Biol Chem. 2007 Apr 20;282(16):12319-29. doi: 10.1074/jbc.M701019200. Epub 2007 Feb 25.
Oligodendrocytes (OLGs) are generated by progenitor cells that are committed to differentiating into myelin-forming cells of the central nervous system. Rearrangement of the cytoskeleton leading to the extension of cellular processes is essential for the myelination of axons by OLGs. Here, we have characterized a new member of the Kelch-related protein family termed MRP2 (for Mayven-related protein 2) that is specifically expressed in brain. MRP2/KLHL1 is expressed in oligodendrocyte precursors and mature OLGs, and its expression is up-regulated during OLG differentiation. MRP2/KLHL1 expression was abundant during the specific stages of oligodendrocyte development, as identified by A2B5-, O4-, and O1-specific oligodendrocyte markers. MRP2/KLHL1 was localized in the cytoplasm and along the cell processes. Moreover, a direct endogenous association of MRP2/KLHL1 with actin was observed, which was significantly increased in differentiated OLGs compared with undifferentiated OLGs. Overexpression of MRP2/KLHL1 resulted in a significant increase in the process extension of rat OLGs, whereas MRP2/KLHL1 antisense reduced the process length of primary rat OLGs. Furthermore, murine OLGs isolated from MRP2/KLHL1 transgenic mice showed a significant increase in the process extension of OLGs compared with control wild-type murine OLGs. These studies provide insights into the role of MRP2/KLHL1, through its interaction with actin, in the process elongation of OLGs.
少突胶质细胞(OLGs)由祖细胞产生,这些祖细胞致力于分化为中枢神经系统中形成髓鞘的细胞。细胞骨架的重排导致细胞突起的延伸,这对于少突胶质细胞对轴突的髓鞘形成至关重要。在这里,我们鉴定了一种与Kelch相关蛋白家族的新成员,称为MRP2(Mayven相关蛋白2),它在脑中特异性表达。MRP2/KLHL1在少突胶质细胞前体和成熟的少突胶质细胞中表达,并且其表达在少突胶质细胞分化过程中上调。通过A2B5、O4和O1特异性少突胶质细胞标志物鉴定,MRP2/KLHL1在少突胶质细胞发育的特定阶段表达丰富。MRP2/KLHL1定位于细胞质和沿细胞突起分布。此外,观察到MRP2/KLHL1与肌动蛋白有直接的内源性结合,与未分化的少突胶质细胞相比,在分化的少突胶质细胞中这种结合显著增加。MRP2/KLHL1的过表达导致大鼠少突胶质细胞的突起延伸显著增加,而MRP2/KLHL1反义寡核苷酸则减少了原代大鼠少突胶质细胞的突起长度。此外,与对照野生型小鼠少突胶质细胞相比,从MRP2/KLHL1转基因小鼠分离的小鼠少突胶质细胞的突起延伸显著增加。这些研究通过MRP2/KLHL1与肌动蛋白的相互作用,深入了解了其在少突胶质细胞突起伸长过程中的作用。