Villegas G M, Haustein A T, Villegas R
Instituto Internacional de Estudios Avanzados (IDEA), Apartado, Caracas, Venezuela.
Brain Res. 1995 Jul 10;685(1-2):77-90. doi: 10.1016/0006-8993(95)00412-j.
The present work deals with the finding and characterization of a neurotrophic factor present in serum-free Dulbecco's modified Eagle's medium in which rat sciatic nerves previously cultured for 9 days were maintained for 24 h. This sciatic nerve conditioned medium (SNCM) produced neuronal differentiation and neurite outgrowth on PC12 cells, as well as survival and differentiation of eight-day old chick embryo dorsal root ganglion (E8-DRG) and ciliary ganglion (E8-CG) neurons. SNCM activity was decreased by dilution, heating and trypsin treatment; it was not inhibited by anti-NGF and anti-bFGF antibodies; and it was not mimicked by CNTF, laminin and fibronectin. By utilizing its neurite-promoting activity on PC12 cells, experiments oriented to purify the factor were carried out. Ultrafiltration, heparin-affinity chromatography and size-exclusion high pressure liquid chromatography (HPLC) were employed. The ability of SNCM to induce PC12 cell, E8-DRG and E8-CG neuronal differentiation, the heparin affinity of the active SNCM protein, and the size-exclusion HPLC elution characteristics of the active protein suggest that the active component of the SNCM is, in all probability, a novel sciatic nerve neurotrophic factor (SNTF).
本研究涉及在无血清的杜氏改良 Eagle 培养基中发现和鉴定一种神经营养因子,该培养基用于维持先前培养 9 天的大鼠坐骨神经 24 小时。这种坐骨神经条件培养基(SNCM)能诱导 PC12 细胞发生神经元分化和神经突生长,还能促进 8 日龄鸡胚背根神经节(E8-DRG)和睫状神经节(E8-CG)神经元的存活与分化。SNCM 的活性会因稀释、加热和胰蛋白酶处理而降低;它不受抗 NGF 和抗 bFGF 抗体的抑制;CNTF、层粘连蛋白和纤连蛋白也无法模拟其活性。利用其对 PC12 细胞的促神经突生长活性,开展了旨在纯化该因子的实验。采用了超滤、肝素亲和层析和尺寸排阻高压液相色谱(HPLC)等方法。SNCM 诱导 PC12 细胞、E8-DRG 和 E8-CG 神经元分化的能力、活性 SNCM 蛋白的肝素亲和性以及活性蛋白的尺寸排阻 HPLC 洗脱特性表明,SNCM 的活性成分很可能是一种新型的坐骨神经神经营养因子(SNTF)。