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在小鼠大脑发育过程中 I 型 ARF 小 GTP 酶 ARF1-3 的表达分析。

Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development.

机构信息

Department of Cellular Pathology, Institute for Developmental Research, Aichi Developmental Disability Center, 713-8 Kamiya, Kasugai, 480-0392, Japan.

Department of Molecular Neurobiology Institute for Developmental Research, Aichi Developmental Disability Center, 713-8 Kamiya, Kasugai, 480-0392, Japan.

出版信息

Mol Biol Rep. 2024 Jan 16;51(1):106. doi: 10.1007/s11033-023-09142-5.

Abstract

BACKGROUND

ARF (ADP-ribosylation factor) GTPases are major regulators of intracellular trafficking, and classified into 3 groups (Type I - III), among which the type I group members, ARF1 and 3, are responsible genes for neurodevelopmental disorders.

METHODS

In this study, we analysed the expression of Type I ARFs ARF1-3 during mouse brain development using biochemical and morphological methods.

RESULTS

Western blotting analyses revealed that ARF1-3 are weakly expressed in the mouse brain at embryonic day 13 and gradually increase until postnatal day 30. ARF1-3 appear to be abundantly expressed in various telencephalon regions. Biochemical fractionation studies detected ARF1-3 in the synaptosome fraction of cortical neurons containing both pre- and post-synapses, however ARF1-3 were not observed in post-synaptic compartments. In immunohistochemical analyses, ARF1-3 appeared to be distributed in the cytoplasm and dendrites of cortical and hippocampal neurons as well as in the cerebellar molecular layer including dendrites of Purkinje cells and granule cell axons. Immunofluorescence in primary cultured hippocampal neurons revealed that ARF1-3 are diffusely distributed in the cytoplasm and dendrites with partial colocalization with a pre-synaptic marker, synaptophysin.

CONCLUSIONS

Overall, our results support the notion that ARF1-3 could participate in vesicle trafficking both in the dendritic shaft (excluding spines) and axon terminals (pre-synaptic compartments).

摘要

背景

ARF(ADP-ribosylation factor)GTPases 是细胞内运输的主要调节剂,分为 3 组(I 型-III 型),其中 I 型组成员 ARF1 和 3 是神经发育障碍的致病基因。

方法

在这项研究中,我们使用生化和形态学方法分析了小鼠大脑发育过程中 I 型 ARFs(ARF1-3)的表达。

结果

Western blot 分析显示,ARF1-3 在胚胎 13 天的小鼠脑中表达较弱,并逐渐增加到出生后 30 天。ARF1-3 似乎在各种端脑区域中大量表达。生化分级分离研究在含有前突触和后突触的皮质神经元的突触体部分检测到 ARF1-3,但在后突触区未观察到 ARF1-3。在免疫组织化学分析中,ARF1-3 似乎分布在皮质和海马神经元的细胞质和树突中,以及包括浦肯野细胞树突和颗粒细胞轴突在内的小脑分子层中。原代培养海马神经元的免疫荧光显示,ARF1-3 在细胞质和树突中弥散分布,与突触小体蛋白(一种前突触标记物)部分共定位。

结论

总的来说,我们的结果支持 ARF1-3 可能参与树突干(不包括棘突)和轴突末梢(前突触区室)中的囊泡运输的观点。

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