Snow D M, Lemmon V, Carrino D A, Caplan A I, Silver J
Case Western Reserve University, Department of Neurosciences, School of Medicine, Cleveland 44106.
Exp Neurol. 1990 Jul;109(1):111-30. doi: 10.1016/s0014-4886(05)80013-5.
In vivo studies of the roof plate of the spinal cord and midline optic tectum in rodent and the developing subplate in the telencephalon of the chick showed that two glycosaminoglycans, keratin sulfate and chondroitin sulfate, possibly in the proteoglycan form (KS-PG, CS-PG, or KS/CS-PG), were present at times when axons approach closely but do not invade these territories. To address the question of whether KS/CS-PG actively inhibits growth cone elongation and to determine which component(s) of the proteoglycan may be critical to this phenomenon, we used a technique employing nitrocellulose-coated petri dishes onto which stripes of various purified macromolecules were attached. Isolated E9 chick dorsal root ganglia were grown on lanes of KS/CS-PG in alteration with lanes of the growth-promoting molecule laminin (LN). Neurite outgrowth was abundant along stripes of LN. In contrast, upon encountering a stripe containing KS/CS-PG, neurites either stopped abruptly or turned and traveled along the KS/CS-PG stripe border. The effect was dependent upon the concentration of the proteoglycan with intermediate concentrations producing intermittent patterns of crossing. We mixed LN with the KS/CS-PG, where the LN was in concentrations which alone support outgrowth, and observed that the KS/CS-PG was still inhibitory when such a growth-promoting molecule was present. A 10-fold higher concentration of LN was able to overcome the inhibitory effect of the KS/CS-PG. These results suggest that the interaction of inhibitory and growth-promoting molecules can interact to produce a wide spectrum of neurite patterns ranging from complete inhibition to totally unimpeded outgrowth. Selective enzymatic removal of the KS or CS from the KS/CS-PG permitted various degrees of neurite outgrowth to occur across the previously inhibitory lanes, and digestion of both glycoaminoglycan moieties, leaving only the protein core of the molecule, resulted in a complete lack of inhibition. These assays demonstrated that KS/CS-PG is inhibitory to embryonic dorsal root ganglia neurites in vitro and that complete inhibition requires contributions from both KS and CS moieties.
对啮齿动物脊髓顶板和中脑中线视顶盖以及鸡端脑发育中的亚板进行的体内研究表明,在轴突靠近但未侵入这些区域时,两种糖胺聚糖,硫酸角质素和硫酸软骨素,可能以蛋白聚糖形式(KS-PG、CS-PG或KS/CS-PG)存在。为了解决KS/CS-PG是否能积极抑制生长锥伸长的问题,并确定蛋白聚糖的哪些成分可能对这一现象至关重要,我们使用了一种技术,即将各种纯化的大分子条带附着在硝酸纤维素包被的培养皿上。将分离的E9鸡背根神经节交替培养在KS/CS-PG条带和促进生长分子层粘连蛋白(LN)条带上。神经突沿着LN条带大量生长。相反,当遇到含有KS/CS-PG的条带时,神经突要么突然停止,要么转向并沿着KS/CS-PG条带边界延伸。这种效应取决于蛋白聚糖的浓度,中等浓度会产生间歇性的交叉模式。我们将LN与KS/CS-PG混合,其中LN的浓度单独就能支持神经突生长,并观察到当存在这种促进生长的分子时,KS/CS-PG仍然具有抑制作用。浓度高出10倍的LN能够克服KS/CS-PG的抑制作用。这些结果表明,抑制性分子和促进生长分子之间的相互作用可以产生广泛的神经突模式,从完全抑制到完全不受阻碍的生长。从KS/CS-PG中选择性酶解去除KS或CS,使得不同程度的神经突生长能够穿过先前具有抑制作用的条带,而消化掉两个糖胺聚糖部分,只留下分子的蛋白核心,则导致完全没有抑制作用。这些实验表明,KS/CS-PG在体外对胚胎背根神经节神经突具有抑制作用,并且完全抑制需要KS和CS部分的共同作用。