Coyle D E
Department of Anesthesia, University of Cincinnati, College of Medicine, Ohio 45267-0531.
J Neurosci Res. 1993 Jul 1;35(4):390-401. doi: 10.1002/jnr.490350406.
The C6 glial cell line has been used as a model cell system for the investigation of new glial produced neurotrophic and neurotropic molecules. By using the C6 cell line grown in a defined medium on collagen, this laboratory has isolated a distinct neurite promoting factor (NPF) that is potentiated by the presence of collagen (CPNPF). We have observed that C6 cells cultured in a defined medium on collagen (rat type-I) slowed their growth rate and expressed an astrocytic- or oligodendrocytic-like morphology. CPNPF, at this state of purity, appears to be a distinct NPF which induces neurite outgrowth (neurites of 1 or more somal diameters) in PC12 cells. These neurite promotion effects, however, appear to support the neuron morphology for only a short period (4 days) of time without the presence of neurotrophic factor (NTF). The neurite promoting activity is ineffective in inducing neurite outgrowth using mouse neuroblastoma cells (neuro-2a). CPNPF appears to be a heat stable protein whose activity does not depend on the presence of intact collagen, heparin sulfate proteoglycan (HSPG), or chondroitin sulfate proteoglycan (CSPG). Exposure to dissociative conditions results in a loss of neurite promoting activity. CPNPF is not a glycoprotein that contains an accessible alpha-D-mannopyranosyl, alpha-D-glucopyranosyl, or a sterically related residue (hydroxyl groups in the C-3,4, and 5 positions). Although these residues are not present on all glycoproteins, it does indicate that CPNPF is most likely not a glycoprotein. CPNPF activity is not blocked by neutralizing antibodies directed toward NGF, beta-FGF, IL-1 beta, IL-6, TGF-beta 2, TGF-beta 1.2, TGF-beta 3, TGF-beta 5, or EGF. CPNPF appears to either be oligomeric protein or a complex of proteins. On the basis of indirect evidence, it does not appear to be glial derived protease nexin-I. The alteration in morphology of the C6 glial cell line by serum-free conditions in the presence of collagen may have induced the production of a potentially new NPF not seen by previous investigators.
C6神经胶质细胞系已被用作一种模型细胞系统,用于研究新的由神经胶质细胞产生的神经营养和向神经分子。通过使用在胶原蛋白上的限定培养基中生长的C6细胞系,本实验室分离出了一种独特的神经突促进因子(NPF),其在胶原蛋白(CPNPF)存在时会增强。我们观察到,在胶原蛋白(大鼠I型)上的限定培养基中培养的C6细胞生长速率减慢,并呈现出星形胶质细胞样或少突胶质细胞样形态。处于这种纯度状态的CPNPF似乎是一种独特的NPF,它能诱导PC12细胞中的神经突生长(神经突长度为1个或更多细胞体直径)。然而,在没有神经营养因子(NTF)的情况下,这些神经突促进作用似乎仅在短时间(4天)内支持神经元形态。使用小鼠神经母细胞瘤细胞(Neuro-2a)时,神经突促进活性在诱导神经突生长方面无效。CPNPF似乎是一种热稳定蛋白,其活性不依赖于完整胶原蛋白、硫酸乙酰肝素蛋白聚糖(HSPG)或硫酸软骨素蛋白聚糖(CSPG)的存在。暴露于解离条件会导致神经突促进活性丧失。CPNPF不是一种含有可及的α-D-甘露吡喃糖基、α-D-葡吡喃糖基或空间相关残基(C-3、4和5位的羟基)的糖蛋白。虽然这些残基并非存在于所有糖蛋白上,但这确实表明CPNPF很可能不是一种糖蛋白。CPNPF的活性不会被针对NGF、β-FGF、IL-1β、IL-6、TGF-β2、TGF-β1.2、TGF-β3、TGF-β5或EGF的中和抗体所阻断。CPNPF似乎要么是寡聚蛋白,要么是蛋白质复合物。基于间接证据,它似乎不是神经胶质细胞衍生的蛋白酶nexin-I。在胶原蛋白存在的情况下,无血清条件对C6神经胶质细胞系形态的改变可能诱导产生了一种先前研究人员未曾发现的潜在新NPF。