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来自肌肉细胞的条件培养基可促进胚胎鸡脊髓神经元的神经突生长。

Neurite outgrowth from embryonic chicken spinal neurons is promoted by media conditioned by muscle cells.

作者信息

Henderson C E, Huchet M, Changeux J P

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2625-9. doi: 10.1073/pnas.78.4.2625.

Abstract

The effect of media conditioned by muscle cells on the development in vitro of chicken spinal neurons was studied. Neural tube cells of 4.5-day chicken embryos were dissociated after trypsinization and cultured in serum-free minimum essential medium conditioned for 4 days over cultures of fused chicken myotubes. After 20 hr in conditioned medium (protein concentration, 10--50 microgram/ml), about 50% of surviving cells had extended neurites, whereas in cultures in nonconditioned medium this value was about 10%. The active factor(s) in conditioned medium is macromolecular and its activity was completely destroyed by incubation with trypsin. Concentrated samples of conditioned medium were analyzed by gel filtration on columns of Sepharose CL-6B. The activity was recovered in peaks with apparent molecular weights of 40,000 and 500,000 and at the exclusion volume of the column. Media conditioned neurite-promoting activity but at lower levels. No activity was detected in Nerve Growth Factor, insulin, fetal calf serum, or horse serum or in media conditioned by chicken lung, chicken heart, or C6 glioma cells.

摘要

研究了经肌肉细胞处理的培养基对鸡脊髓神经元体外发育的影响。4.5日龄鸡胚的神经管细胞经胰蛋白酶消化后解离,并在无血清的最低必需培养基中培养,该培养基在融合的鸡肌管培养物上处理4天。在条件培养基(蛋白质浓度为10 - 50微克/毫升)中培养20小时后,约50%的存活细胞长出了神经突,而在非条件培养基中培养的细胞,这一比例约为10%。条件培养基中的活性因子是大分子,其活性经胰蛋白酶孵育后完全被破坏。用Sepharose CL - 6B柱对条件培养基的浓缩样品进行凝胶过滤分析。活性在表观分子量为40,000和500,000的峰以及柱的排阻体积处恢复。培养基具有促进神经突生长的活性,但水平较低。在神经生长因子、胰岛素、胎牛血清或马血清中,以及在鸡肺、鸡心或C6胶质瘤细胞处理的培养基中均未检测到活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35d8/319402/9e4adcf7e4b8/pnas00655-0669-a.jpg

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