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微管相关蛋白2C样构建体的表达诱导Sf9细胞中的过程形成。

Process formation in Sf9 cells induced by the expression of a microtubule-associated protein 2C-like construct.

作者信息

LeClerc N, Kosik K S, Cowan N, Pienkowski T P, Baas P W

机构信息

Harvard Medical School, Boston, MA 02115.

出版信息

Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6223-7. doi: 10.1073/pnas.90.13.6223.

DOI:10.1073/pnas.90.13.6223
PMID:8327502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC46900/
Abstract

To understand the roles of various microtubule-associated proteins (MAPs) in the development of axons and dendrites, we have expressed individual neuronal MAPs in normally rounded Sf9 host cells. We previously reported that expression of tau protein in these cells results in the elaboration of long processes containing dense bundles of microtubules (MTs). These bundles generally terminate in the hillock region of the cell body, and almost all of the MTs within the bundles are oriented with their plus ends distal to the cell body. Here we report the expression of a construct that approximates the MAP2C sequence and also induces the elaboration of processes with dense bundles of predominantly plus-end-distal MTs. Whereas tau generally results in a single process, there is a significantly greater tendency for the MAP2C-like construct to induce multiple processes. In contrast to the tau processes, the MT bundle in these processes extends far into the cell body. This latter observation suggests that MAP2C and tau have different effects on MT assembly and/or transport events in the cell. Although both of these MAPs can organize MTs that are competent to participate in process formation, the detailed organization of MTs induced by each of the two constructs is distinctive, and these differences may be relevant to axonal and dendritic differentiation.

摘要

为了解各种微管相关蛋白(MAPs)在轴突和树突发育中的作用,我们在通常呈圆形的Sf9宿主细胞中表达了单个神经元MAPs。我们之前报道过,在这些细胞中表达tau蛋白会导致形成含有密集微管束(MTs)的长突起。这些微管束通常在细胞体的小丘区域终止,并且束内几乎所有的微管其正端都朝向远离细胞体的方向。在此我们报道了一种近似MAP2C序列的构建体的表达情况,并发现它也能诱导形成含有密集微管束且主要是正端远离细胞体的突起。虽然tau通常会导致形成单个突起,但类似MAP2C的构建体诱导形成多个突起的倾向明显更大。与tau诱导形成的突起不同,这些突起中的微管束会深入延伸到细胞体内。后一观察结果表明,MAP2C和tau对细胞内微管组装和/或运输事件有不同影响。尽管这两种MAPs都能组织有能力参与突起形成的微管,但这两种构建体各自诱导形成的微管的详细组织方式是不同的,这些差异可能与轴突和树突的分化有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/0bde4ed2f6a9/pnas01470-0358-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/0ea54924abce/pnas01470-0355-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/fb057cfb0457/pnas01470-0356-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/f76b0246a0e8/pnas01470-0357-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/0bde4ed2f6a9/pnas01470-0358-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/0ea54924abce/pnas01470-0355-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/fb057cfb0457/pnas01470-0356-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/f76b0246a0e8/pnas01470-0357-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5134/46900/0bde4ed2f6a9/pnas01470-0358-a.jpg

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