Katoh-Semba R, Oohira A, Kashiwamata S
Department of Perinatology, Aichi Prefecture Colony, Japan.
J Neurochem. 1992 Jul;59(1):282-9. doi: 10.1111/j.1471-4159.1992.tb08902.x.
Structural changes in proteoglycans (PGs) were examined during the neuritogenesis of PC12 cells induced by nerve growth factor (NGF). (1) A heparan sulfate (HS) PG and a chondroitin sulfate (CS) PG were synthesized by PC12 cells, irrespective of the presence of NGF or the duration of culture. PGs released from PC12 cells into the culture medium were mostly CSPGs. (2) In the absence of NGF, the apparent molecular mass of HSPG prepared from PC12 cells after 3 days of culture was in the range of 90-190 kDa for the intact form (Kav = 0.38 on Sepharose CL-6B), 12 kDa for HS, and 61 kDa for the core protein. In the presence of NGF, these values were 90-190 kDa, 10 kDa, and 51 kDa and 61 kDa, respectively. The intact forms of cell-associated CSPG had apparent molecular mass ranges of 120-150 kDa and 120-190 kDa (Kav = 0.38 and 0.34), with CSs of 15 kDa and 20 kDa in the presence and absence of NGF, respectively. The apparent molecular mass of the core protein of cell-associated CSPG was 92 kDa, irrespective of the presence of NGF. The molecular sizes of cell-associated PGs and their glycosaminoglycans remained unchanged during culture. (3) CSPGs released by PC12 cells into the culture medium were separated into two peaks (I and II) by column chromatography on DEAE-cellulose. The peak II fraction prepared from the medium with NGF after 3 days of culture consisted of CSPG with Kav = 0.22 on Sephacryl S-300 [40-84 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)].(ABSTRACT TRUNCATED AT 250 WORDS)
在神经生长因子(NGF)诱导PC12细胞发生神经突生长的过程中,对蛋白聚糖(PGs)的结构变化进行了研究。(1)无论有无NGF或培养时间长短,PC12细胞均可合成硫酸乙酰肝素(HS)PG和硫酸软骨素(CS)PG。从PC12细胞释放到培养基中的PGs大多为CSPGs。(2)在无NGF的情况下,培养3天后从PC12细胞制备的HSPG的完整形式的表观分子量范围为90 - 190 kDa(在Sepharose CL - 6B上的Kav = 0.38),HS为12 kDa,核心蛋白为61 kDa。在有NGF的情况下,这些值分别为90 - 190 kDa、10 kDa以及51 kDa和61 kDa。细胞相关CSPG的完整形式的表观分子量范围为120 - 150 kDa和120 - 190 kDa(Kav = 0.38和0.34),在有和无NGF时CS分别为15 kDa和20 kDa。细胞相关CSPG核心蛋白的表观分子量为92 kDa,与有无NGF无关。在培养过程中,细胞相关PGs及其糖胺聚糖的分子大小保持不变。(3)PC12细胞释放到培养基中的CSPGs通过DEAE - 纤维素柱层析分离为两个峰(I和II)。培养3天后从含NGF的培养基中制备的峰II级分由在Sephacryl S - 300上Kav = 0.22的CSPG组成[通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)为40 - 84 kDa]。(摘要截断于250字)