Role of lipoproteins in the delivery of lipids to axons during axonal regeneration

被引:146
作者
de Chaves, EIP
Rusiñol, AE
Vance, DE
Campenot, RB
Vance, JE [1 ]
机构
[1] Univ Alberta, Lipid & Lipoprot Res Grp, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2S2, Canada
[3] Univ Alberta, Dept Cell Biol & Anat, Edmonton, AB T6G 2S2, Canada
[4] Univ Alberta, Dept Med, Edmonton, AB T6G 2S2, Canada
关键词
D O I
10.1074/jbc.272.49.30766
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
Nerve fiber elongation involves the input of lipids to the growing axons. Since cell bodies are often a great distance from the regenerating tips, alternative sources of lipids have been proposed. We previously demonstrated that axonal synthesis of phosphatidylcholine is required for axonal growth (Posse de Chaves, E., Vance, D. E., Campenot, R. B. and Vance, J. E. (1995) J. Cell Biol, 128, 913-918; Posse de Chaves, E., Vance, D. E., Campenot, R. B. and Vance, J. E. (1995) Biochem, J. 312, 411-417), In contrast, cholesterol is not made in axons. We now show that when compartmented cultures of rat sympathetic neurons are incubated with pravastatin, in the absence of exogenously supplied lipids, cholesterol synthesis is inhibited and axonal growth is impaired. The addition of cholesterol to the axons or cell bodies of neurons treated with this inhibitor restores normal axonal elongation. Similarly, a supply of cholesterol via lipoproteins restores normal axonal growth. In contrast, lipoproteins do not provide axons with sufficient phosphatidylcholine for normal elongation when axonal phosphatidylcholine synthesis is inhibited. Thus, our studies support the idea that during axonal regeneration lipoproteins can be taken up by axons from the microenvironment and supply sufficient cholesterol, but not phosphatidylcholine, for growth, We also show that neither apoE nor apoA-I within the lipoproteins is essential for axonal growth.
引用
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页码:30766 / 30773
页数:8
相关论文
共 48 条
  • [1] Identification of scavenger receptor SR-BI as a high density lipoprotein receptor
    Acton, S
    Rigotti, A
    Landschulz, KT
    Xu, SZ
    Hobbs, HH
    Krieger, M
    [J]. SCIENCE, 1996, 271 (5248) : 518 - 520
  • [2] ALBERTS B, 1989, MOL BIOL CELL, P1059
  • [3] BEUCHE W, 1984, J NEUROCYTOL, V13, P767, DOI 10.1007/BF01148493
  • [4] BASIS FOR PHOSPHOLIPID INCORPORATION INTO PERIPHERAL-NERVE MYELIN
    BOIRON, F
    SPIVACK, WD
    DESHMUKH, DS
    GOULD, RM
    [J]. JOURNAL OF NEUROCHEMISTRY, 1993, 60 (01) : 320 - 329
  • [5] A ROLE FOR APOLIPOPROTEIN-E, APOLIPOPROTEIN-A-I, AND LOW-DENSITY LIPOPROTEIN RECEPTORS IN CHOLESTEROL TRANSPORT DURING REGENERATION AND REMYELINATION OF THE RAT SCIATIC-NERVE
    BOYLES, JK
    ZOELLNER, CD
    ANDERSON, LJ
    KOSIK, LM
    PITAS, RE
    WEISGRABER, KH
    HUI, DY
    MAHLEY, RW
    GEBICKEHAERTER, PJ
    IGNATIUS, MJ
    SHOOTER, EM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (03) : 1015 - 1031
  • [6] BROUSSEAU T, 1993, CLIN CHEM, V39, P960
  • [7] CAMPENOT RB, 1991, J NEUROSCI, V11, P1126
  • [8] GROWTH OF SYMPATHETIC-NERVE FIBERS IN CULTURE DOES NOT REQUIRE EXTRACELLULAR CALCIUM
    CAMPENOT, RB
    DRAKER, DD
    [J]. NEURON, 1989, 3 (06) : 733 - 743
  • [9] CAMPENOT RB, 1992, CELL CELL INTERACTIO, P275
  • [10] DETERMINATION OF LIPID PHOSPHORUS IN NANOMOLAR RANGE
    CHALVARDJIAN, A
    RUDNICKI, E
    [J]. ANALYTICAL BIOCHEMISTRY, 1970, 36 (01) : 225 - +