Hagihara K, Miura R, Kosaki R, Berglund E, Ranscht B, Yamaguchi Y
The Burnham Institute, La Jolla, California 92037, USA.
J Comp Neurol. 1999 Jul 26;410(2):256-64.
Brevican is one of the most abundant chondroitin sulfate proteoglycans in the adult rat brain. We have recently shown that the C-type lectin domain of brevican binds fibronectin type III domains 3-5 of tenascin-R. Here we report strong evidence for a physiological basis for this interaction. Substantial brevican immunoreactivity was detected in a number of nuclei and in the reticular formations throughout the midbrain and hindbrain, including, but not limited to, the deep cerebellar nuclei, the trapezoid body, the red nucleus, the oculomotor nucleus, the vestibular nucleus, the cochlear nucleus, the gigantocellular reticular nucleus, the motor trigeminal nucleus, and the lateral superior olive. Most of the brevican immunoreactivity exhibited pericellular and reticular staining patterns. In almost all of these sites, brevican immunoreactivity colocalized with that of tenascin-R, which was also substantially codistributed with versican, another member of the lectican family. Detailed analysis revealed that the pericellular staining of brevican resembled that in perineuronal nets in which tenascin-R has been localized. Immunoelectron microscopy identified brevican immunoreactivity in the intercellular spaces surrounding presynaptic boutons and on their surfaces, but not in the synaptic clefts or in their immediate vicinity, a distribution pattern consistent with perineuronal nets. Taken together, our results provide strong evidence that the previously reported interactions between brevican and tenascin-R may play a functional role within the perineuronal nets.
短蛋白聚糖是成年大鼠脑中含量最丰富的硫酸软骨素蛋白聚糖之一。我们最近发现,短蛋白聚糖的C型凝集素结构域与腱生蛋白-R的III型纤连蛋白结构域3-5结合。在此,我们报告了这一相互作用存在生理基础的有力证据。在中脑和后脑的许多核团及网状结构中检测到大量的短蛋白聚糖免疫反应性,包括但不限于小脑深部核团、斜方体、红核、动眼神经核、前庭核、耳蜗核、巨细胞网状核、运动三叉神经核和外侧上橄榄核。大多数短蛋白聚糖免疫反应性呈现细胞周围和网状染色模式。在几乎所有这些部位,短蛋白聚糖免疫反应性与腱生蛋白-R的免疫反应性共定位,腱生蛋白-R也与凝集素家族的另一个成员多功能蛋白聚糖大量共分布。详细分析显示,短蛋白聚糖的细胞周围染色类似于已定位有腱生蛋白-R的神经元周围网中的染色。免疫电子显微镜在突触前终扣周围的细胞间隙及其表面鉴定出短蛋白聚糖免疫反应性,但在突触间隙或其紧邻区域未检测到,这种分布模式与神经元周围网一致。综上所述,我们的结果提供了有力证据,表明先前报道的短蛋白聚糖与腱生蛋白-R之间的相互作用可能在神经元周围网中发挥功能作用。