Two novel mammalian Nogo receptor homologs differentially expressed in the central and peripheral nervous systems

被引:67
作者
Laurén, J [1 ]
Airaksinen, MS [1 ]
Saarma, M [1 ]
Timmusk, T [1 ]
机构
[1] Univ Helsinki, Program Mol Neurobiol, Inst Biotechnol, FIN-00014 Helsinki, Finland
关键词
nerve redeneration; myelm; receptor; nervous system; in situ hybridisation; leucine-rich repeat; GPI-anchor; Nogo; prostate cancer overexpressed gene I;
D O I
10.1016/S1044-7431(03)00199-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The regenerative capacity of the adult mammalian central nervous system is restricted by the myelinating oligodendrocytes that form a nonpermissive environment for axonal growth. Currently only the Nogo receptor (NgR), in complex with p75(NTR) neurotrophin receptor is known to be involved in this inhibitory signalling in neurons. NgR is a common receptor for the three inhibitory myelin proteins Nogo-A, OMgp, and MAG. Here we describe two novel Nogo receptor gene homologs named NGRL2 and NGRL3 from human and mouse that, like NGR, encode putative leucine-rich repeat containing GPI-anchored proteins. We show by in situ hybridisation and by RT-PCR that NGRL mRNAs are predominantly expressed in the neurons of the embryonic and adult central and peripheral nervous systems, and that they together with NGR possess distinct and partially nonoverlapping expression patterns. We also show that all four members of the reticulon family, including Nogo-A, are widely expressed in the nervous system, and therefore are possible ligands for the NgRLs. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:581 / 594
页数:14
相关论文
共 44 条
[21]   INVERSE PATTERNS OF MYELINATION AND GAP-43 EXPRESSION IN THE ADULT CNS - NEURITE GROWTH-INHIBITORS AS REGULATORS OF NEURONAL PLASTICITY [J].
KAPFHAMMER, JP ;
SCHWAB, ME .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 340 (02) :194-206
[22]   SUPPRESSION OF THE ONSET OF MYELINATION EXTENDS THE PERMISSIVE PERIOD FOR THE FUNCTIONAL REPAIR OF EMBRYONIC SPINAL-CORD [J].
KEIRSTEAD, HS ;
HASAN, SJ ;
MUIR, GD ;
STEEVES, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (24) :11664-11668
[23]   The leucine-rich repeat as a protein recognition motif [J].
Kobe, B ;
Kajava, AV .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2001, 11 (06) :725-732
[24]   A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system [J].
Laurén, J ;
Airaksinen, MS ;
Saarma, M ;
Timmusk, T .
GENOMICS, 2003, 81 (04) :411-421
[25]   Link of a new type of apoptosis-inducing gene ASY/Nogo-B to human cancer [J].
Li, Q ;
Qi, B ;
Oka, K ;
Shimakage, M ;
Yoshioka, N ;
Inoue, H ;
Hakura, A ;
Kodama, K ;
Stanbridge, EJ ;
Yutsudo, M .
ONCOGENE, 2001, 20 (30) :3929-3936
[26]   Myelin-associated glycoprotein as a functional ligand for the Nogo-66 receptor [J].
Liu, BP ;
Fournier, A ;
GrandPré, T ;
Strittmatter, SM .
SCIENCE, 2002, 297 (5584) :1190-1193
[27]   IDENTIFICATION OF MYELIN-ASSOCIATED GLYCOPROTEIN AS A MAJOR MYELIN-DERIVED INHIBITOR OF NEURITE GROWTH [J].
MCKERRACHER, L ;
DAVID, S ;
JACKSON, DL ;
KOTTIS, V ;
DUNN, RJ ;
BRAUN, PE .
NEURON, 1994, 13 (04) :805-811
[28]   Extensive genomic duplication during early chordate evolution [J].
McLysaght, A ;
Hokamp, K ;
Wolfe, KH .
NATURE GENETICS, 2002, 31 (02) :200-204
[29]   A NOVEL ROLE FOR MYELIN-ASSOCIATED GLYCOPROTEIN AS AN INHIBITOR OF AXONAL REGENERATION [J].
MUKHOPADHYAY, G ;
DOHERTY, P ;
WALSH, FS ;
CROCKER, PR ;
FILBIN, MT .
NEURON, 1994, 13 (03) :757-767
[30]   Nogo and its paRTNers [J].
Oertle, T ;
Schwab, ME .
TRENDS IN CELL BIOLOGY, 2003, 13 (04) :187-194