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在培养过程中,雪旺细胞基底膜沉积和无髓鞘交感神经轴突的包裹需要成纤维细胞。

Fibroblasts are required for Schwann cell basal lamina deposition and ensheathment of unmyelinated sympathetic neurites in culture.

作者信息

Obremski V J, Johnson M I, Bunge M B

机构信息

Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

J Neurocytol. 1993 Feb;22(2):102-17. doi: 10.1007/BF01181574.

Abstract

The ability to purify and recombine populations of peripheral neurons, Schwann cells and fibroblasts in tissue culture has enabled us to examine the contribution of fibroblasts to Schwann cell basal lamina assembly and ensheathment of unmyelinated rat superior cervical ganglion neurites in vitro. Purified perinatal superior cervical ganglion neurons were grown in culture either with Schwann cells or with Schwann cells plus fibroblasts derived from either superior cervical ganglion capsule or cranial periosteum. The cultures were maintained for 2-8 weeks on a collagen substratum in a medium known to promote Schwann cell differentiation (myelin, basal lamina formation) in the presence of dorsal root ganglion neurons. The extent of Schwann cell differentiation (ensheathment, basal lamina formation) in the presence of superior cervical ganglion neurons was evaluated in this study using electron microscopy. In superior cervical ganglion neuron plus Schwann cell cultures (without fibroblasts), Schwann cells achieved only a moderate degree of ensheathment; also, Schwann cell basal lamina was discontinuous and extracellular collagen fibrils were sparse. Although only discontinuous basal lamina was demonstrable by electron microscopy in these cultures, surprisingly, Schwann cell/neurite fascicles were uniformly immunostained for laminin, type IV collagen, and heparan sulfate proteoglycan. The addition of fibroblasts to superior cervical ganglion neuron plus Schwann cell cultures increased the deposition of basal lamina around the Schwann cell/neurite units, the number of collagen fibrils, and the extent of neurite ensheathment. We propose that the presence of basal lamina increases the Schwann cell's ability to ensheathe superior cervical ganglion neurites, possibly through an augmentation of specific extracellular matrix components or by increasing in some way the capacity of these components to become organized into basal lamina. We conclude that, unlike dorsal root ganglion neurons, superior cervical ganglion neurons are unable to stimulate full Schwann cell extracellular matrix expression with the result that these Schwann cells require the extraneuronal influence of fibroblasts to deposit basal lamina and attain their mature phenotype in culture.

摘要

在组织培养中纯化和重组外周神经元、施万细胞和成纤维细胞群体的能力,使我们能够在体外研究成纤维细胞对施万细胞基底膜组装以及大鼠无髓鞘颈上神经节神经突包被的作用。纯化的围产期颈上神经节神经元在培养时,要么与施万细胞一起培养,要么与来源于颈上神经节被膜或颅骨骨膜的施万细胞和成纤维细胞一起培养。在已知能促进施万细胞分化(髓鞘形成、基底膜形成)的培养基中,将这些培养物在胶原基质上维持2至8周,同时存在背根神经节神经元。本研究使用电子显微镜评估在颈上神经节神经元存在的情况下施万细胞分化(包被、基底膜形成)的程度。在颈上神经节神经元加施万细胞培养物(无成纤维细胞)中,施万细胞仅实现了中等程度的包被;此外,施万细胞基底膜不连续,细胞外胶原纤维稀少。尽管在这些培养物中通过电子显微镜仅能观察到不连续的基底膜,但令人惊讶的是,施万细胞/神经突束对层粘连蛋白、IV型胶原和硫酸乙酰肝素蛋白聚糖进行了均匀的免疫染色。在颈上神经节神经元加施万细胞培养物中添加成纤维细胞,增加了施万细胞/神经突单位周围基底膜的沉积、胶原纤维的数量以及神经突包被的程度。我们提出,基底膜的存在可能通过增加特定细胞外基质成分或通过以某种方式提高这些成分组织成基底膜的能力,来增强施万细胞包被颈上神经节神经突的能力。我们得出结论,与背根神经节神经元不同,颈上神经节神经元无法刺激施万细胞充分表达细胞外基质,结果是这些施万细胞需要成纤维细胞的神经元外影响来沉积基底膜并在培养中获得其成熟表型。

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