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蛋白脂蛋白和髓鞘碱性蛋白在培养的小鼠少突胶质细胞中的分布:原代培养与传代培养

Distribution of proteolipid protein and myelin basic protein in cultured mouse oligodendrocytes: primary vs. secondary cultures.

作者信息

Konola L T, Tyler B M, Yamamura T, Lees M B

机构信息

Department of Biochemistry, E.K. Shriver Center, Waltham, Massachusetts 02254.

出版信息

J Neurosci Res. 1991 Jan;28(1):49-64. doi: 10.1002/jnr.490280106.

DOI:10.1002/jnr.490280106
PMID:1710282
Abstract

The distribution of proteolipid protein (PLP) and myelin basic protein (MBP) was examined in differentiating oligodendrocytes of primary and secondary mouse brain cell cultures by single- and double-label indirect immunofluorescence. In primary cultures, MBP and PLP were differentially located in oligodendrocytes. MBP became concentrated as fine punctate dots lining the edges of processes and as coarse grains in flattened sheet-like structures. PLP was distributed diffusely throughout cell bodies and processes but was limited to the perimeter of sheets and some processes within sheets. To compare the detailed distribution of PLP and MBP in the absence of underlying cells, a simple method for the growth of isolated oligodendrocytes in secondary cultures was developed. Cells were maintained in primary culture for 39-41 days, harvested by scraping, enriched for oligodendrocytes, and plated at low cell density. After 1 week, isolated oligodendrocytes had developed long processes and large flattened membranous sheets. MBP and PLP were differentially localized in these cell structures. The sheets contained fine-grained patches of MBP, which were surrounded by networks of MBP- processes. In contrast, PLP was initially seen throughout the cell bodies and processes. In older cultures, PLP became strikingly concentrated in curvilinear membranous profiles. The observations show that PLP and MBP are differentially located in cultured mouse oligodendrocytes. Furthermore, the precise distribution of these myelin-specific antigens is dependent on culture conditions.

摘要

通过单标记和双标记间接免疫荧光法,研究了原代和传代小鼠脑细胞培养物中分化的少突胶质细胞中蛋白脂蛋白(PLP)和髓鞘碱性蛋白(MBP)的分布。在原代培养物中,MBP和PLP在少突胶质细胞中的定位不同。MBP集中在沿突起边缘排列的细点状以及扁平片状结构中的粗颗粒中。PLP弥漫分布于整个细胞体和突起,但局限于片状结构的周边以及片层内的一些突起。为了比较在没有下层细胞情况下PLP和MBP的详细分布,开发了一种在传代培养中培养分离少突胶质细胞的简单方法。细胞在原代培养中维持39 - 41天,通过刮取收获,富集少突胶质细胞,并以低密度接种。1周后,分离的少突胶质细胞长出了长突起和大的扁平膜状片层。MBP和PLP在这些细胞结构中的定位不同。片层中含有细颗粒状的MBP斑块,周围是MBP阳性突起网络。相比之下,PLP最初在整个细胞体和突起中都可见。在较老的培养物中,PLP显著集中在线性膜状结构中。这些观察结果表明,PLP和MBP在培养的小鼠少突胶质细胞中的定位不同。此外,这些髓鞘特异性抗原的精确分布取决于培养条件。

相似文献

1
Distribution of proteolipid protein and myelin basic protein in cultured mouse oligodendrocytes: primary vs. secondary cultures.蛋白脂蛋白和髓鞘碱性蛋白在培养的小鼠少突胶质细胞中的分布:原代培养与传代培养
J Neurosci Res. 1991 Jan;28(1):49-64. doi: 10.1002/jnr.490280106.
2
Microtubule associated protein (MAP1B) is present in cultured oligodendrocytes and co-localizes with tubulin.微管相关蛋白(MAP1B)存在于培养的少突胶质细胞中,并与微管蛋白共定位。
J Neurosci Res. 1990 Sep;27(1):112-24. doi: 10.1002/jnr.490270117.
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Role for the oligodendrocyte cytoskeleton in myelination.少突胶质细胞细胞骨架在髓鞘形成中的作用。
J Neurosci Res. 1989 Apr;22(4):439-48. doi: 10.1002/jnr.490220409.
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Glial conditioned medium enables jimpy oligodendrocytes to express properties of normal oligodendrocytes: production of myelin antigens and membranes.神经胶质细胞条件培养基能使jimpy少突胶质细胞表达正常少突胶质细胞的特性:产生髓磷脂抗原和膜。
Glia. 1988;1(4):253-9. doi: 10.1002/glia.440010404.
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Orientation of the myelin proteolipid protein C-terminus in oligodendroglial membranes.少突胶质细胞膜中髓鞘蛋白脂蛋白C末端的取向
Glia. 1992;5(2):112-21. doi: 10.1002/glia.440050205.
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Plasma membrane of cultured oligodendrocytes: III. Relatedness to myelin.培养的少突胶质细胞的质膜:III. 与髓磷脂的相关性。
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Spatial distribution of myelin basic protein mRNA and polypeptide in quaking oligodendrocytes in culture.培养的震颤少突胶质细胞中髓鞘碱性蛋白mRNA和多肽的空间分布。
J Neurosci Res. 1991 Jul;29(3):271-81. doi: 10.1002/jnr.490290302.
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Intracellular distribution of myelin protein gene products is altered in oligodendrocytes of the taiep rat.在泰耶普大鼠的少突胶质细胞中,髓磷脂蛋白基因产物的细胞内分布发生了改变。
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Regional expression of myelin protein genes in the developing mouse brain: in situ hybridization studies.发育中小鼠大脑中髓磷脂蛋白基因的区域表达:原位杂交研究
J Neurosci Res. 1988 Oct-Dec;21(2-4):238-48. doi: 10.1002/jnr.490210216.

引用本文的文献

1
Induction of oligodendrocyte differentiation and in vitro myelination by inhibition of rho-associated kinase.通过抑制Rho相关激酶诱导少突胶质细胞分化和体外髓鞘形成
ASN Neuro. 2014 Jun 25;6(4):1759091414538134. doi: 10.1177/1759091414538134.
2
Orientation of myelin proteolipid protein in the oligodendrocyte cell membrane.髓磷脂蛋白脂蛋白在少突胶质细胞膜中的定位。
Neurochem Res. 1996 Apr;21(4):431-40. doi: 10.1007/BF02527707.
3
Novel oligodendrocyte transmembrane signaling systems. Investigations utilizing antibodies as ligands.
新型少突胶质细胞跨膜信号系统。利用抗体作为配体的研究。
Mol Neurobiol. 1993 Spring;7(1):1-22. doi: 10.1007/BF02780606.