Powell E M, Geller H M
Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Glia. 1999 Mar;26(1):73-83. doi: 10.1002/(sici)1098-1136(199903)26:1<73::aid-glia8>3.0.co;2-s.
Neurites are believed to be guided by astrocyte boundaries during development. We have previously shown that in vitro astrocyte boundaries can be generated by combining two different astrocyte cell lines, one which is inhibitory to neurite outgrowth (Neu7) with one that is permissive (A7). The extracellular matrix molecules tenascin-C, chondroitin sulfate proteoglycans (CSPG) and keratan sulfate proteoglycans (KSPG) were implicated in boundary formation. We have now further addressed the roles of these molecules using additional astrocyte cell lines that differ in their potential to permit neurite extension and in their expression of extracellular matrix molecules. T34-2 and 27A1 cells are permissive to neurite extension. T34-2 cells express high amounts of tenascin-C, but very low levels of proteoglycans, while 27A1 cells express CSPG and KSPG, but very little tenascin-C. T34-2 cells formed boundaries to neurites, and these boundaries are greatly reduced in the presence of blocking antitenascin-C antiserum. The addition of the antiserum did not affect neurite extension. 27A1 cells also formed boundaries without affecting neurite extension. Chondroitinase ABC, but not keratanase, treatment reduced the boundary, suggesting that CSPG is a major boundary component. These results demonstrate that astrocyte tenascin-C and proteoglycans are distinct components of astrocyte boundaries. More importantly, these results suggest that growing neurites can be directed to their targets by astrocyte-derived guidance molecules independent of effects on process extension.
人们认为在发育过程中,神经突是由星形胶质细胞边界引导的。我们之前已经表明,在体外,通过将两种不同的星形胶质细胞系结合,可以生成星形胶质细胞边界,一种对神经突生长具有抑制作用(Neu7),另一种则具有促进作用(A7)。细胞外基质分子腱生蛋白-C、硫酸软骨素蛋白聚糖(CSPG)和硫酸角质素蛋白聚糖(KSPG)与边界形成有关。我们现在使用了另外一些星形胶质细胞系,这些细胞系在允许神经突延伸的潜力以及细胞外基质分子的表达方面存在差异,进一步研究了这些分子的作用。T34-2和27A1细胞允许神经突延伸。T34-2细胞表达大量的腱生蛋白-C,但蛋白聚糖水平非常低,而27A1细胞表达CSPG和KSPG,但腱生蛋白-C含量很少。T34-2细胞与神经突形成边界,并且在存在阻断抗腱生蛋白-C抗血清的情况下,这些边界会大大减少。添加抗血清并不影响神经突的延伸。27A1细胞也形成了边界,且不影响神经突的延伸。用软骨素酶ABC而不是角质素酶处理可减少边界,这表明CSPG是边界的主要成分。这些结果表明,星形胶质细胞的腱生蛋白-C和蛋白聚糖是星形胶质细胞边界的不同组成部分。更重要的是,这些结果表明,生长中的神经突可以由星形胶质细胞衍生的导向分子引导至其靶点,而与对突起延伸的影响无关。