Kalb R G, Hockfield S
Section of Neuroanatomy, Yale University School of Medicine, New Haven, CT 06510.
Neuroscience. 1990;34(2):391-401. doi: 10.1016/0306-4522(90)90148-w.
The expression of a cell surface proteoglycan, recognized by monoclonal antibody Cat-301, is regulated by neuronal activity in early life. Here we report that the expression of the Cat-301 proteoglycan on motor neurons depends on primary afferent input in the early postnatal period. Previously we showed that in two different systems, Y-cells in the cat lateral geniculate nucleus and motor neurons in the hamster spinal cord, the expression of the Cat-301 antigen requires neuronal activity during a circumscribed period in development. Disrupting the activity of Y-cells (by dark rearing or by monocular lid suture) or of motor neurons (by sciatic nerve crush or by spinal cord lesion) during the early postnatal period prevents Cat-301 expression. Disrupting neuronal activity in adults has no effect on Cat-301 expression. The onset of Cat-301 expression corresponds to the end of the period of activity-dependent development. In order to further dissect the components of the segmental reflex are required for the expression of Cat-301 on motor neurons, here we evaluated the effect of deafferentation by dorsal rhizotomy. In adult animals two weeks after deafferentation all sciatic motor neurons continue to express Cat-301. In contrast, in neonates two weeks after deafferentation the normal developmental expression of Cat-301 is reduced and less than 50% of sciatic motor neurons express Cat-301. We next selectively lesioned the small diameter afferents using the neurotoxin capsaicin. In contrast to rhizotomy, neonatal deletion of small diameter afferents has no effect on the development of Cat-301 expression on motor neurons. These results imply that input relayed by large diameter primary afferents (probably those conveying muscle and/or joint information) is required for normal maturation of motor neuronal properties during early life. They also provide further evidence for activity-dependent maturation of motor neurons.
一种可被单克隆抗体Cat - 301识别的细胞表面蛋白聚糖的表达,在生命早期受神经元活动调控。在此我们报告,运动神经元上Cat - 301蛋白聚糖的表达在出生后早期依赖于初级传入输入。此前我们表明,在两个不同系统中,即猫外侧膝状核的Y细胞和仓鼠脊髓的运动神经元,Cat - 301抗原的表达在发育的特定时期需要神经元活动。在出生后早期破坏Y细胞(通过暗饲养或单眼眼睑缝合)或运动神经元(通过坐骨神经挤压或脊髓损伤)的活动会阻止Cat - 301表达。在成年动物中破坏神经元活动对Cat - 301表达没有影响。Cat - 301表达的开始对应于活动依赖发育时期的结束。为了进一步剖析运动神经元上Cat - 301表达所需的节段性反射弧的组成部分,在此我们评估了背根切断去传入的影响。在成年动物去传入两周后,所有坐骨运动神经元继续表达Cat - 301。相比之下,在新生动物去传入两周后,Cat - 301的正常发育表达减少,不到50%的坐骨运动神经元表达Cat - 301。接下来我们使用神经毒素辣椒素选择性损伤小直径传入纤维。与背根切断不同,新生动物小直径传入纤维的缺失对运动神经元上Cat - 301表达的发育没有影响。这些结果表明,大直径初级传入纤维(可能是那些传递肌肉和/或关节信息的纤维)传递的输入是生命早期运动神经元特性正常成熟所必需的。它们也为运动神经元的活动依赖成熟提供了进一步的证据。