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The formation from the Schwann cell surface of myelin in the peripheral nerves of chick embryos.鸡胚周围神经中髓磷脂从施万细胞表面形成的过程。
Exp Cell Res. 1954 Nov;7(2):558-62. doi: 10.1016/s0014-4827(54)80098-x.
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Role of glypican-1 in the trophic activity on PC12 cells induced by cultured sciatic nerve conditioned medium: identification of a glypican-1-neuregulin complex.磷脂酰肌醇蛋白聚糖-1在培养的坐骨神经条件培养基诱导的PC12细胞营养活性中的作用:磷脂酰肌醇蛋白聚糖-1-神经调节蛋白复合物的鉴定
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Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth.少突胶质细胞髓鞘糖蛋白是一种抑制神经突生长的Nogo受体配体。
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Ionic currents in PC12 cells differentiated into neuron-like cells by a cultured-sciatic nerve conditioned medium.经培养的坐骨神经条件培养基分化为类神经元细胞的PC12细胞中的离子电流。
Brain Res. 2001 Aug 24;911(2):181-92. doi: 10.1016/s0006-8993(01)02683-x.
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Neuregulin found in cultured-sciatic nerve conditioned medium causes neuronal differentiation of PC12 cells.
Brain Res. 2000 Jan 10;852(2):305-18. doi: 10.1016/s0006-8993(99)02109-5.
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Nogo in nerve regeneration.神经再生中的Nogo蛋白
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Neuregulins in glial cells.
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Schwann cells express NDF and SMDF/n-ARIA mRNAs, secrete neuregulin, and show constitutive activation of erbB3 receptors: evidence for a neuregulin autocrine loop.施万细胞表达神经生长因子(NDF)和SMDF/n-ARIA信使核糖核酸(mRNAs),分泌神经调节蛋白,并显示erbB3受体的组成性激活:神经调节蛋白自分泌环的证据。
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10
Expression of neuregulins and their putative receptors, ErbB2 and ErbB3, is induced during Wallerian degeneration.在沃勒氏变性过程中,神经调节蛋白及其假定受体ErbB2和ErbB3的表达被诱导。
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用坐骨神经、视神经或雪旺细胞条件培养基处理的PC12细胞的神经元样分化。

Neuron-like differentiation of PC12 cells treated with media conditioned by either sciatic nerves, optic nerves, or Schwann cells.

作者信息

Villegas Raimundo, Villegas Gloria M, Núñez Jorge, Hernández Marianela, Castillo Cecilia

机构信息

Centro de Biociencias y Medicina Molecular, Instituto de Estudios Avanzados-IDEA, Caracas, Venezuela.

出版信息

Cell Mol Neurobiol. 2005 Mar;25(2):451-61. doi: 10.1007/s10571-005-3153-9.

DOI:10.1007/s10571-005-3153-9
PMID:16047552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11529543/
Abstract

In previous works we reported the finding of neurotrophic activity in a serum-free Dulbecco's modified Eagle's medium conditioned by rat sciatic nerves, previously maintained in culture for 11 days. This medium produces rapid neuron-like differentiation of cultured PC12 cells, as revealed by an increase in the size of the cell body and by the extension of short and/or long neurites by most of the cells. Neuregulin present in the conditioned medium was demonstrated to play a key role in the observed differentiation. In the present work, taking into consideration those latter results, the neurotrophic activity of conditioned media prepared with sciatic and optic nerves cultured during days 1-4 and 9-12 were studied. Evaluation of the trophic activities of those media revealed an opposite timing in the activities of sciatic and optic nerves conditioned media. The activity of the sciatic nerve was not observed in the 1-4-day period, increasing then up to the 9-12-day period. On the contrary, the optic nerve conditioned medium was active in the 1-4-day period, decreasing down to the 9-12-day period. These results led us to explore the contribution of the different cellular constituents of those nerves to their neurotrophic properties. As a first step in that direction we also investigated the neurotrophic activity of media conditioned during 12 days by cultured Schwann cells isolated from rat sciatic nerves. The Schwann cell conditioned media did produce a rapid differentiation of the PC12 cells similar to that caused by the sciatic nerve conditioned medium, though of a lower magnitude. Variations in the trophic activities of the conditioned media used in the present work is discussed taking into consideration the production of trophic and inhibitory factors by the peripheral and central glial cells. The role played by the optic nerve glia and myelin is being investigated at present.

摘要

在先前的研究中,我们报道了在由大鼠坐骨神经条件培养11天的无血清杜氏改良 Eagle 培养基中发现神经营养活性。这种培养基能使培养的PC12细胞迅速发生神经元样分化,表现为细胞体增大,且大多数细胞伸出短和/或长的神经突。已证明条件培养基中存在的神经调节蛋白在观察到的分化过程中起关键作用。在本研究中,考虑到这些结果,我们研究了用培养1 - 4天和9 - 12天的坐骨神经和视神经制备的条件培养基的神经营养活性。对这些培养基的营养活性评估显示,坐骨神经和视神经条件培养基的活性时间相反。坐骨神经的活性在1 - 4天期间未观察到,随后增加直至9 - 12天期间。相反,视神经条件培养基在1 - 4天期间有活性,到9 - 12天期间下降。这些结果促使我们探索这些神经的不同细胞成分对其神经营养特性的贡献。作为该方向的第一步,我们还研究了从大鼠坐骨神经分离的培养雪旺细胞在12天内条件培养的培养基的神经营养活性。雪旺细胞条件培养基确实使PC12细胞迅速分化,类似于坐骨神经条件培养基引起的分化,尽管程度较低。本文讨论了本研究中使用的条件培养基营养活性的变化,并考虑了外周和中枢神经胶质细胞产生的营养和抑制因子。目前正在研究视神经胶质细胞和髓鞘所起的作用。