Process elongation of oligodendrocytes is promoted by the kelch-related protein MRP2/KLHL1

被引:22
作者
Jiang, Shuxian [1 ]
Seng, Seyha [1 ]
Avraham, Hava Karsenty [1 ]
Fu, Yigong [1 ]
Avraham, Shalom [1 ]
机构
[1] Harvard Univ, Sch Med, Div Expt Med, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
关键词
D O I
10.1074/jbc.M701019200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:12319 / 12329
页数:11
相关论文
共 50 条
  • [21] kel-1, a novel Kelch-related gene in Caenorhabditis elegans is expressed in pharyngeal gland cells and is required for the feeding process. (vol 4, pg 325, 1999)
    Ohmachi, M
    Sugimoto, A
    Iino, Y
    Yamamoto, M
    GENES TO CELLS, 1999, 4 (08) : 487 - 487
  • [22] ATP-dependent transport of glutathione S-conjugates by the multidrug resistance protein MRP1 and its apical isoform MRP2
    Keppler, D
    Leier, I
    Jedlitschky, G
    König, J
    CHEMICO-BIOLOGICAL INTERACTIONS, 1998, 112 : 153 - 161
  • [23] Gene and protein expression of P-glycoprotein, MRP1, MRP2, and CYP3A4 in the small and large human intestine
    Berggren, Sofia
    Gall, Christine
    Wollnitz, Nadine
    Ekelund, Mats
    Karlbom, Urban
    Hoogstraate, Janet
    Schrenk, Dieter
    Lennernas, Hans
    MOLECULAR PHARMACEUTICS, 2007, 4 (02) : 252 - 257
  • [24] Direct evidence that saquinavir is transported by multidrug resistance-associated protein (MRP1) and canalicular multispecific organic anion transporter (MRP2)
    Williams, GC
    Liu, A
    Knipp, G
    Sinko, PJ
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) : 3456 - 3462
  • [25] A new monoclonal antibody, P2A8(6), that specifically recognizes a novel epitope on the multidrug resistance-associated protein 1 (MRP1), but not on MRP2 nor MRP3
    Connolly, L
    Moran, E
    Larkin, A
    Scheffer, G
    Scheper, R
    Sarkadi, B
    Kool, M
    Clynes, M
    HYBRIDOMA AND HYBRIDOMICS, 2001, 20 (5-6): : 333 - 341
  • [26] Identification of drugs and drug metabolites as substrates of multidrug resistance protein 2 (MRP2) using triple-transfected MDCK-OATP1B1-UGT1A1-MRP2 cells
    Fahrmayr, C.
    Koenig, J.
    Auge, D.
    Mieth, M.
    Fromm, M. F.
    BRITISH JOURNAL OF PHARMACOLOGY, 2012, 165 (06) : 1836 - 1847
  • [27] Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines
    Kool, M
    deHaas, M
    Scheffer, GL
    Scheper, RJ
    vanEijk, MJT
    Juijn, JA
    Baas, F
    Borst, P
    CANCER RESEARCH, 1997, 57 (16) : 3537 - 3547
  • [28] Modulation of human multidrug resistance protein (MRP) 1 (ABCC1) and MRP2 (ABCC2) transport activities by endogenous and exogenous glutathione-conjugated catechol metabolites
    Slot, Andrew J.
    Wise, Dana D.
    Deeley, Roger G.
    Monks, Terrence J.
    Cole, Susan P. C.
    DRUG METABOLISM AND DISPOSITION, 2008, 36 (03) : 552 - 560
  • [29] Involvement of sulfate conjugation and multidrug resistance-associated protein 2 (Mrp2) in sex-related differences in the pharmacokinetics of garenoxacin in rats
    Hayashi, Tamon
    Abe, Fumie
    Kato, Miki
    Saito, Hiroko
    Ueyama, Jun
    Kondo, Yuya
    Imai, Kuniyuki
    Katoh, Miki
    Nadai, Masayuki
    Hasegawa, Takaaki
    JOURNAL OF INFECTION AND CHEMOTHERAPY, 2011, 17 (01) : 24 - 29
  • [30] The potential role of human multidrug resistance protein 1 (MDR1) and multidrug resistance-associated protein 2 (MRP2) in the transport of Huperzine A in vitro
    Fei, Ziyan
    Hu, Mengyun
    Baum, Larry
    Kwan, Patrick
    Hong, Tao
    Zhang, Chunbo
    XENOBIOTICA, 2020, 50 (03) : 354 - 362