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蛋白激酶C底物B-50/GAP43在分离的突触前神经终末和神经元生长锥中的超微结构免疫细胞化学定位。

Ultrastructural immunocytochemical localization of B-50/GAP43, a protein kinase C substrate, in isolated presynaptic nerve terminals and neuronal growth cones.

作者信息

Van Lookeren Campagne M, Oestreicher A B, Van Bergen en Henegowen P M, Gispen W H

机构信息

Division of Molecular Neurobiology Rudolf Magnus Institute, University of Utrecht, The Netherlands.

出版信息

J Neurocytol. 1989 Aug;18(4):479-89. doi: 10.1007/BF01474544.

DOI:10.1007/BF01474544
PMID:2809634
Abstract

Accumulating evidence indicates that the neuron-specific B-50/GAP43, a substrate for protein kinase C, plays a role in neuronal differentiation and neuritogenesis during nervous tissue development and axonal regeneration. An ultrastructural immunocytochemical study on the localization of B-50 in presynaptic terminals (synaptosomes) isolated from the frontal cortex of 6-week-old rats, and in neuronal growth cones, isolated from forebrains of 5-day-old rats, the majority of B-50 is detected at the surrounding neuronal plasma membrane. In both neuronal growth cones and synaptosomes, a relatively small fraction of B-50 in the cytoplasm was not evidently associated with internal membranes. Our results indicate that B-50 is mainly located at the cytoplasmic face of the synaptosomal and neuronal growth cone plasma membrane. The similar B-50 localization in neuronal growth cones and synaptosomes suggests that, both in extending axons and mature synaptic terminals, B-50 may exert identical functions as a protein kinase C substrate at the plasma membrane.

摘要

越来越多的证据表明,神经元特异性B-50/GAP43作为蛋白激酶C的底物,在神经组织发育和轴突再生过程中的神经元分化和神经突形成中发挥作用。一项超微结构免疫细胞化学研究,对从6周龄大鼠额叶皮质分离的突触前终末(突触体)以及从5日龄大鼠前脑分离的神经元生长锥中B-50的定位进行了研究,发现大部分B-50存在于周围的神经元质膜上。在神经元生长锥和突触体中,细胞质中相对少量的B-50并未明显与内膜相关联。我们的结果表明,B-50主要位于突触体和神经元生长锥质膜的胞质面。B-50在神经元生长锥和突触体中的相似定位表明,在延伸的轴突和成熟的突触终末中,B-50作为质膜上的蛋白激酶C底物可能发挥相同的功能。

相似文献

1
Ultrastructural immunocytochemical localization of B-50/GAP43, a protein kinase C substrate, in isolated presynaptic nerve terminals and neuronal growth cones.蛋白激酶C底物B-50/GAP43在分离的突触前神经终末和神经元生长锥中的超微结构免疫细胞化学定位。
J Neurocytol. 1989 Aug;18(4):479-89. doi: 10.1007/BF01474544.
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Synapsin I (Protein I), a nerve terminal-specific phosphoprotein. II. Its specific association with synaptic vesicles demonstrated by immunocytochemistry in agarose-embedded synaptosomes.突触素I(蛋白I),一种神经末梢特异性磷蛋白。II. 通过免疫细胞化学在琼脂糖包埋的突触体中证明其与突触小泡的特异性结合。
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Immunocytochemical distribution of the protein kinase C substrate B-50 (GAP43) in developing rat pyramidal tract.蛋白激酶C底物B-50(GAP43)在发育中的大鼠锥体束中的免疫细胞化学分布
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GAP-43 distribution is correlated with development of growth cones and presynaptic terminals.生长相关蛋白43(GAP-43)的分布与生长锥和突触前终末的发育相关。
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Muscarinic receptor activation stimulates B-50/GAP43 phosphorylation in isolated nerve growth cones.毒蕈碱受体激活可刺激分离出的神经生长锥中的B-50/GAP43磷酸化。
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Development of neuronal polarity: GAP-43 distinguishes axonal from dendritic growth cones.神经元极性的发育:GAP - 43区分轴突生长锥与树突生长锥。
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Light and electron microscopic localization of B-50 (GAP43) in the rat spinal cord during transganglionic degenerative atrophy and regeneration.经神经节变性萎缩和再生过程中大鼠脊髓中B-50(GAP43)的光镜和电镜定位
J Neurosci Res. 1992 May;32(1):93-109. doi: 10.1002/jnr.490320112.

引用本文的文献

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Adenoviral vector-mediated expression of B-50/GAP-43 induces alterations in the membrane organization of olfactory axon terminals in vivo.腺病毒载体介导的B-50/GAP-43表达在体内诱导嗅轴突终末膜组织发生改变。
J Neurosci. 1997 Sep 1;17(17):6575-86. doi: 10.1523/JNEUROSCI.17-17-06575.1997.
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Purification of B-50 by 2-mercaptoethanol extraction from rat brain synaptosomal plasma membranes.
通过2-巯基乙醇从大鼠脑突触体细胞膜中提取纯化B-50。
Neurochem Res. 1993 Aug;18(8):875-81. doi: 10.1007/BF00998271.
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Immunocytochemical localization of a growth-associated protein (GAP-43) in rat adrenal gland.大鼠肾上腺中生长相关蛋白(GAP - 43)的免疫细胞化学定位
Cell Tissue Res. 1994 Mar;275(3):555-66. doi: 10.1007/BF00318824.
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Light-microscopic study of phosphoprotein B-50 in myopathies.肌病中磷蛋白B - 50的光镜研究。
Virchows Arch. 1995;426(1):69-76. doi: 10.1007/BF00194700.
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4-Aminopyridine stimulates B-50 (GAP-43) phosphorylation in rat synaptosomes.4-氨基吡啶刺激大鼠突触体中B-50(GAP-43)的磷酸化。
J Mol Neurosci. 1990;2(1):11-7. doi: 10.1007/BF02896921.
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Mol Neurobiol. 1991;5(2-4):61-85. doi: 10.1007/BF02935540.
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Monoclonal antibodies show that kinase C phosphorylation of GAP-43 during axonogenesis is both spatially and temporally restricted in vivo.单克隆抗体显示,轴突形成过程中GAP - 43的蛋白激酶C磷酸化在体内在空间和时间上均受到限制。
J Cell Biol. 1991 Mar;112(5):991-1005. doi: 10.1083/jcb.112.5.991.