Glial lipoproteins stimulate axon growth of central nervous system neurons in compartmented cultures

被引:149
作者
Hayashi, H
Campenot, RB
Vance, DE
Vance, JE [1 ]
机构
[1] Univ Alberta, Dept Med, Grp Mol & Cell Biol Lipids, HMRC 328, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Dept Cell Biol, Edmonton, AB T6G 2S2, Canada
[3] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2S2, Canada
[4] Univ Alberta, Canadian Inst Hlth, Res Grp Mol & Cell Biol Lipids, Edmonton, AB T6G 2S2, Canada
关键词
D O I
10.1074/jbc.M313828200
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
The role of lipoproteins secreted by cortical glial cells in axon growth of central nervous system (CNS) neurons was investigated. We first established compartmented cultures of CNS neurons ( retinal ganglion cells). Addition of glial cell-conditioned medium (GCM) to distal axons increased the rate of axon extension by similar to 50%. Inhibition of 3-hydroxy-3-methylglutaryl-CoA reductase in glial cells diminished the secretion of cholesterol and apolipoprotein E, and prevented the growth stimulatory effect of GCM. When glia-derived lipoproteins containing apolipoprotein E were provided to distal axons, axon extension was stimulated to the same extent as by GCM. In contrast, addition of lipoproteins to cell bodies failed to enhance growth. The growth stimulatory effect of glial lipoproteins was abrogated in the presence of receptor-associated protein, RAP, indicating involvement of receptor(s) of the low density lipoprotein receptor family in stimulation of axonal extension. These observations suggest that glial cells stimulate axon growth of CNS neurons by providing lipoproteins containing cholesterol and apolipoprotein E to distal axons.
引用
收藏
页码:14009 / 14015
页数:7
相关论文
共 71 条
[61]   Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2 [J].
Trommsdorff, M ;
Gotthardt, M ;
Hiesberger, T ;
Shelton, J ;
Stockinger, W ;
Nimpf, J ;
Hammer, RE ;
Richardson, JA ;
Herz, J .
CELL, 1999, 97 (06) :689-701
[62]   Preferential utilization of newly synthesized cholesterol for brain growth in neonatal lambs [J].
Turley, SD ;
Burns, DK ;
Dietschy, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1998, 274 (06) :E1099-E1105
[63]   Control of synapse number by glia [J].
Ullian, EM ;
Sapperstein, SK ;
Christopherson, KS ;
Barres, BA .
SCIENCE, 2001, 291 (5504) :657-661
[64]   ISOLATION AND ANALYSIS OF LIPOPROTEINS SECRETED BY RAT-LIVER HEPATOCYTES [J].
VANCE, DE ;
WEINSTEIN, DB ;
STEINBERG, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 792 (01) :39-47
[65]  
VANCE JE, 1994, J NEUROCHEM, V62, P329
[66]   BIOSYNTHESIS OF MEMBRANE-LIPIDS IN RAT AXONS [J].
VANCE, JE ;
PAN, D ;
VANCE, DE ;
CAMPENOT, RB .
JOURNAL OF CELL BIOLOGY, 1991, 115 (04) :1061-1068
[67]   Glia-neuron intercommunications and synaptic plasticity [J].
Vernadakis, A .
PROGRESS IN NEUROBIOLOGY, 1996, 49 (03) :185-214
[68]  
WEISGRABER KH, 1994, ADV PROTEIN CHEM, V45, P249
[69]  
WOLF BB, 1992, AM J PATHOL, V141, P37
[70]   Elements of neural adhesion molecules and a yeast vacuolar protein sorting receptor are present in a novel mammalian low density lipoprotein receptor family member [J].
Yamazaki, H ;
Bujo, H ;
Kusunoki, J ;
Seimiya, K ;
Kanaki, T ;
Morisaki, N ;
Schneider, WJ ;
Saito, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (40) :24761-24768