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从发育中的人类坐骨神经培养的细胞中层粘连蛋白和胶原蛋白基因的表达。

Expression of laminin and collagen genes by cells cultured from developing human sciatic nerves.

作者信息

Hirvonen O M, Peltonen S A, Hirvonen H E, Björkstrand A S, Peltonen J T

机构信息

Department of Medical Biochemistry, University of Turku, Finland.

出版信息

J Peripher Nerv Syst. 1996;1(1):42-52.

Abstract

The expression of laminin alpha1, alpha2, beta1, beta2 and gamma1 subunits and proalpha1(I), proalpha1(III), alpha1(IV), alpha1(VI), alpha2(VI) and alpha3(VI) collagen chains was studied by Northern hybridizations, RNase protection assays and indirect immunofluorescence (IIF) labellings in cell cultures initiated from sciatic nerves of 14-27-wk-old human fetuses. The cultures represented mixed populations of Schwann cells, perineurial cells and fibroblasts, as estimated by morphology and S 100 protein immunolabellings. The mRNAs for certain basement membrane (BM) components, laminin beta1 and gamma1 chains and collagen alpha1(IV) chain, were readily detectable by Northern analyses in all cultures. In contrast, laminin alpha1, alpha2 and beta2 chain mRNAs were expressed at markedly lower levels. The expression of laminin alpha1 chain was detectable only by RNase protection assay. RNase protection analysis also demonstrated that the expression of laminin alpha2 chain increased with the developmental stage of the nerve used as the source for cell cultures. The expression of laminin beta2 chain was detected only at the protein level by IIF which demonstrated a faint immunosignal in a small subpopulation of cells. The mRNAs for type I, III and VI collagens were readily detectable in the cultures by Northern hybridizations. In summary, the extracellular matrix genes expressed in fetal human peripheral nerves and corresponding cell cultures display marked similarities. Cell cultures characterized here may prove useful in analyses elucidating potential roles of selected growth factors and cytokines in the induction of e.g. laminin alpha1 and beta2 chain expression by cells of developing peripheral nerves.

摘要

通过Northern杂交、核糖核酸酶保护分析和间接免疫荧光(IIF)标记,对取自14至27周龄人类胎儿坐骨神经的细胞培养物中纤连蛋白α1、α2、β1、β2和γ1亚基以及前α1(I)、前α1(III)、α1(IV)、α1(VI)、α2(VI)和α3(VI)胶原链的表达进行了研究。根据形态学和S100蛋白免疫标记估计,这些培养物代表了雪旺细胞、神经束膜细胞和成纤维细胞的混合群体。通过Northern分析,在所有培养物中都很容易检测到某些基底膜(BM)成分、纤连蛋白β1和γ1链以及胶原α1(IV)链的mRNA。相比之下,纤连蛋白α1、α2和β2链mRNA的表达水平明显较低。仅通过核糖核酸酶保护分析可检测到纤连蛋白α1链的表达。核糖核酸酶保护分析还表明,纤连蛋白α2链的表达随着用作细胞培养源的神经的发育阶段而增加。仅通过IIF在蛋白质水平检测到纤连蛋白β2链的表达,在一小部分细胞亚群中显示出微弱的免疫信号。通过Northern杂交在培养物中很容易检测到I型、III型和VI型胶原的mRNA。总之,在胎儿人类外周神经和相应细胞培养物中表达的细胞外基质基因显示出明显的相似性。这里表征的细胞培养物可能有助于分析阐明选定的生长因子和细胞因子在诱导发育中的外周神经细胞表达例如纤连蛋白α1和β2链中的潜在作用。

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