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γ-氨基丁酸能生长锥:内源性γ-氨基丁酸的释放先于突触小泡抗原的表达。

GABAergic growth cones: release of endogenous gamma-aminobutyric acid precedes the expression of synaptic vesicle antigens.

作者信息

Taylor J, Docherty M, Gordon-Weeks P R

机构信息

Biomedical Sciences Division, King's College London, England.

出版信息

J Neurochem. 1990 May;54(5):1689-99. doi: 10.1111/j.1471-4159.1990.tb01223.x.

Abstract

Growth cone fractions isolated from neonatal [postnatal day 3 (P3)] rat forebrain contain GABAergic growth cones as demonstrated by immunofluorescence staining with monospecific antibodies to gamma-aminobutyric acid (GABA). HPLC analysis shows that GABAergic growth cones release this endogenous GABA when stimulated with high K+. Endogenous GABA release is Ca2(+)-independent and, in this respect, similar to that seen previously with [3H]GABA. Isolated growth cone fractions also exhibit a K(+)-stimulated, Ca2(+)-independent release of endogenous taurine. None of the other amino acids shown to be present in isolated growth cone fractions were released, including glutamate, aspartate, and glycine. A population of dissociated cerebral cortical neurones prepared from P1 rat forebrain were GABA-immunoreactive after 1 day in culture. The cell body, neurites, and growth cones of these neurones were all stained with GABA antibodies. At this time in culture, neurones did not stain with either of two antibodies to synaptic vesicle antigens, i.e., p65 and synaptophysin. Growth cones isolated from P3 rat forebrain were also not immunoreactive with these antibodies. After about 8 days in culture, when neurones had established extensive networks of long, varicose axons and elaborately branched dendrites, many neurones and their neurites were immunoreactive for GABA antibodies. At this time in culture, p65 and synaptophysin antibodies did stain neuronal cell bodies and particularly their varicose axons. Dendrites were not stained with synaptic vesicle antibodies. These results suggest that GABAergic neurones synthesize GABA during neurite outgrowth and that GABA is present in, and can be released from, the growth cones of these neurones. The presence of GABA in GABAergic growth cones is not associated with synaptic vesicles, which explains the Ca2+ independency of both endogenous and [3H]GABA release from these growth cones.

摘要

从新生大鼠(出生后第3天,P3)前脑分离出的生长锥部分含有γ-氨基丁酸(GABA)能生长锥,这通过用γ-氨基丁酸(GABA)单特异性抗体进行免疫荧光染色得以证明。高效液相色谱分析表明,GABA能生长锥在受到高钾刺激时会释放这种内源性GABA。内源性GABA的释放不依赖于Ca2+,在这方面,与之前用[3H]GABA观察到的情况相似。分离出的生长锥部分还表现出钾离子刺激的、不依赖于Ca2+的内源性牛磺酸释放。在分离出的生长锥部分中显示存在的其他氨基酸,包括谷氨酸、天冬氨酸和甘氨酸,均未释放。从P1大鼠前脑制备的一群解离的大脑皮质神经元在培养1天后具有GABA免疫反应性。这些神经元的细胞体、神经突和生长锥均被GABA抗体染色。在培养的这个阶段,神经元未被两种突触小泡抗原抗体(即p65和突触素)染色。从P3大鼠前脑分离出的生长锥也与这些抗体没有免疫反应性。在培养约8天后,当神经元建立了广泛的长而有曲张的轴突和复杂分支的树突网络时,许多神经元及其神经突对GABA抗体具有免疫反应性。在培养的这个阶段,p65和突触素抗体确实对神经元细胞体尤其是其曲张的轴突进行了染色。树突未被突触小泡抗体染色。这些结果表明,GABA能神经元在神经突生长过程中合成GABA,并且GABA存在于这些神经元的生长锥中并可从其中释放。GABA能生长锥中GABA的存在与突触小泡无关,这解释了内源性和[3H]GABA从这些生长锥释放均不依赖于Ca2+的原因。

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