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培养的发育中神经元中Stathmin和SCG10的差异分布。

Differential distribution of stathmin and SCG10 in developing neurons in culture.

作者信息

Di Paolo G, Lutjens R, Osen-Sand A, Sobel A, Catsicas S, Grenningloh G

机构信息

Geneva Biomedical Research Institute, Glaxo Wellcome Research and Development S.A., Switzerland.

出版信息

J Neurosci Res. 1997 Dec 15;50(6):1000-9. doi: 10.1002/(SICI)1097-4547(19971215)50:6<1000::AID-JNR10>3.0.CO;2-8.

Abstract

The neuron-specific protein SCG10 and the ubiquitous protein stathmin are two members of a family of microtubule-destabilizing factors that may regulate microtubule dynamics in response to extracellular signals. To gain insight into the function of these proteins in the nervous system, we have compared their intracellular distribution in cortical neurons developing in culture. We have used double-immunofluorescence microscopy with specific antibodies for stathmin and SCG10 in combination with antibodies for axonal, microtubule, and synaptic marker proteins. Stathmin and SCG10 were coexpressed in individual neurons. While both proteins were highly expressed in developing cultures during differentiation, their subcellular localization was strikingly different. Stathmin showed a cytosolic distribution, mainly in cell bodies, whereas SCG10 strongly labeled the growth cones of axons and dendrites. During neurite outgrowth, SCG10 appeared as a single concentrated spot in a region of the growth cone where the microtubules are known to be particularly dynamic. Disassembly of labile microtubules by nocodazole caused a dispersal of the SCG10 staining into punctate structures, indicating that its subcellular localization is microtubule-dependent. Upon maturation and synapse formation, the levels of both stathmin and SCG10 decreased to become undetectable. These observations demonstrate that the expression of both proteins is associated with neurite outgrowth and suggest that they perform their roles in this process in distinct subcellular compartments.

摘要

神经元特异性蛋白SCG10和普遍存在的蛋白stathmin是微管解聚因子家族的两个成员,它们可能响应细胞外信号调节微管动力学。为深入了解这些蛋白在神经系统中的功能,我们比较了它们在体外培养的皮质神经元中的细胞内分布。我们使用了针对stathmin和SCG10的特异性抗体进行双重免疫荧光显微镜检查,并结合了轴突、微管和突触标记蛋白的抗体。Stathmin和SCG10在单个神经元中共表达。虽然这两种蛋白在分化过程中的发育培养物中均高表达,但它们的亚细胞定位却显著不同。Stathmin呈胞质分布,主要在细胞体中,而SCG10则强烈标记轴突和树突的生长锥。在神经突生长过程中,SCG10在生长锥的一个区域呈现为单个浓缩斑点,已知该区域的微管特别活跃。诺考达唑对不稳定微管的拆解导致SCG10染色分散成点状结构,表明其亚细胞定位依赖于微管。在成熟和突触形成后,stathmin和SCG10的水平均下降至无法检测到。这些观察结果表明,这两种蛋白的表达均与神经突生长相关,并表明它们在这一过程中在不同的亚细胞区室中发挥作用。

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