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与培养底物结合的条件培养基因子诱导神经突生长。

Induction of neurite outgrowth by a conditioned-medium factor bound to the culture substratum.

作者信息

Collins F

出版信息

Proc Natl Acad Sci U S A. 1978 Oct;75(10):5210-3. doi: 10.1073/pnas.75.10.5210.

DOI:10.1073/pnas.75.10.5210
PMID:217018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC336295/
Abstract

Heart-cell conditioned medium (HCM) induces rapid neurite outgrowth from isolated neurons in culture. The following evidence indicates that this action of HCM is due to a trypsin-sensitive factor which attaches to the polyornithinecoated culture substratum: (i) Pretreatment of the culture substratum with HCM allows rapid neurite outgrowth to occur even in unconditioned media. The active factor remains bound to the substratum during the period of neurite outgrowth. (ii) The substratum-bound activity is destroyed by trypsin treatment, but is insensitive to collagenase, RNase, and DNase. (iii) The factor that binds to the substratum is essential for neurite outgrowth, because HCM is no longer active when the material that binds to the polyornithine substratum has been removed by passage of the HCM over a series of culture dishes. However, this "depleted" HCM is still able to support the growth of nonneuronal cells. (iv) Most significantly, when neurons are cultured in whole HCM, the extent of neurite outgrowth is proportional to the amount of substratum-bound activity and not to the amount in solution, indicating that the substratum-bound form of the factor is more active. Previous observations [Collins, F. (1978) Dev. Biol. 65, 50-57] suggest that HCM promotes neurite outgrowth by increasing the adhesion between nerve cell surface extensions and the polyornithine-coated culture substratum. It is possible, therefore, that the factor in HCM that binds to the substratum possesses sites to which nerve cell surface components adhere.

摘要

心脏细胞条件培养基(HCM)可诱导培养的分离神经元快速长出神经突。以下证据表明,HCM的这种作用归因于一种对胰蛋白酶敏感的因子,该因子附着于聚鸟氨酸包被的培养底物上:(i)用HCM预处理培养底物,即使在未条件化的培养基中也能使神经突快速长出。在神经突生长期间,活性因子仍与底物结合。(ii)底物结合活性可被胰蛋白酶处理破坏,但对胶原酶、核糖核酸酶和脱氧核糖核酸酶不敏感。(iii)与底物结合的因子对神经突生长至关重要,因为当通过一系列培养皿使HCM通过后,与聚鸟氨酸底物结合的物质被去除时,HCM就不再具有活性。然而,这种“耗尽的”HCM仍能支持非神经元细胞的生长。(iv)最显著的是,当神经元在全HCM中培养时,神经突生长的程度与底物结合活性的量成正比,而与溶液中的量无关,这表明因子的底物结合形式更具活性。先前的观察结果[柯林斯,F.(1978年)《发育生物学》65卷,第50 - 57页]表明,HCM通过增加神经细胞表面延伸与聚鸟氨酸包被的培养底物之间的黏附来促进神经突生长。因此,HCM中与底物结合的因子可能具有神经细胞表面成分可附着的位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b604/336295/b58df5627a70/pnas00669-0585-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b604/336295/b58df5627a70/pnas00669-0585-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b604/336295/b58df5627a70/pnas00669-0585-a.jpg

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本文引用的文献

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The expression of differentiation by chick embryo thyroid in cell culture. I. Functional and fine structural stability in mass and clonal culture.鸡胚甲状腺在细胞培养中的分化表达。I. 群体培养和克隆培养中的功能及精细结构稳定性
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Axon initiation by ciliary neurons in culture.培养的睫状神经元的轴突起始
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