Giger R J, Wolfer D P, De Wit G M, Verhaagen J
Graduate School Neurosciences Amsterdam, Netherlands Institute for Brain Research, The Netherlands.
J Comp Neurol. 1996 Nov 18;375(3):378-92. doi: 10.1002/(SICI)1096-9861(19961118)375:3<378::AID-CNE3>3.0.CO;2-#.
Semaphorin III/collapsin-1 (semaIII/coll-1) is a chemorepellent that exhibits a repulsive effect on growth cones of dorsal root ganglion neurons. To identify structures that express semaIII/coll-1 in developing mammals, we cloned the rat homologue and performed in situ hybridization on embryonic, neonatal, and adult rats. The relationship between semaIII/coll-1 mRNA distribution and developing nerve tracts was studied by combining in situ hybridization with immunohistochemistry for markers of growing nerve fibers. At embryonic day 11, semaIII/coll-1 expression was restricted to the olfactory pit, the basal and rostral surface of the telencephalic vesicle, the anlage of the eye, the epithelium of Rathke's pouch, and the somites. At later developmental stages, semaIII/coll-1 mRNA was found to be widely distributed in neuronal as well as in mesenchymal and epithelial structures outside the nervous system. Strong expression was found in the olfactory bulb, retina, lens, piriform cortex, amygdalostriatal area, pons, cerebellar anlage, motor nuclei of cranial nerves, and ventral spinal cord. After birth, mesenchymal staining decreased rapidly and expression became progressively restricted to specific sets of neurons in the central nervous system (CNS). In the mature CNS, semaIII/coll-1 mRNA remains detectable in mitral cells, neurons of the accessory bulb and cerebral cortex, cerebellar Purkinje cells, as well as a subset of cranial and spinal motoneurons. The temporal and spatial expression pattern of semaIII/coll-1 mRNA and its relationship to emerging nerve tracts suggests that semaIII/coll-1 is involved in guiding growing axons towards their targets by forming a molecular boundary that instructs axons to engage in the formation of specific nerve tracts.
信号素III/萎缩蛋白-1(semaIII/coll-1)是一种化学排斥剂,对背根神经节神经元的生长锥具有排斥作用。为了确定发育中的哺乳动物中表达semaIII/coll-1的结构,我们克隆了大鼠同源物,并对胚胎期、新生期和成年大鼠进行了原位杂交。通过将原位杂交与针对生长神经纤维标记物的免疫组织化学相结合,研究了semaIII/coll-1 mRNA分布与发育中神经束之间的关系。在胚胎第11天,semaIII/coll-1的表达局限于嗅窝、端脑泡的基底和嘴侧表面、眼原基、拉特克囊的上皮以及体节。在发育后期,发现semaIII/coll-1 mRNA广泛分布于神经系统外的神经元以及间充质和上皮结构中。在嗅球、视网膜、晶状体、梨状皮质、杏仁核纹状体区、脑桥、小脑原基、脑神经运动核和脊髓腹侧发现了强烈表达。出生后,间充质染色迅速减少,表达逐渐局限于中枢神经系统(CNS)中的特定神经元群。在成熟的CNS中,仍可在二尖瓣细胞、副嗅球和大脑皮质的神经元、小脑浦肯野细胞以及一部分脑神经和脊髓运动神经元中检测到semaIII/coll-1 mRNA。semaIII/coll-1 mRNA的时空表达模式及其与新兴神经束的关系表明,semaIII/coll-1通过形成分子边界来引导生长中的轴突朝向其靶标,该分子边界指导轴突参与特定神经束的形成。