Clarris H J, Key B
Department of Anatomy and Cell Biology, The University of Melbourne, Parkville, VIC 3052, Australia.
J Neurobiol. 2001 Feb 5;46(2):113-25. doi: 10.1002/1097-4695(20010205)46:2<113::aid-neu40>3.0.co;2-0.
The main olfactory and the accessory olfactory systems are both anatomically and functionally distinct chemosensory systems. The primary sensory neurones of the accessory olfactory system are sequestered in the vomeronasal organ (VNO), where they express pheromone receptors, which are unrelated to the odorant receptors expressed in the principal nasal cavity. We have identified a 240 kDa glycoprotein (VNO(240)) that is selectively expressed by sensory neurones in the VNO but not in the main olfactory neuroepithelium of mouse. VNO(240) is first expressed at embryonic day 20.5 by a small subpopulation of sensory neurones residing within the central region of the crescent-shaped VNO. Although VNO(240) was detected in neuronal perikarya at this age, it was not observed in the axons in the accessory olfactory bulb until postnatal day 3.5. This delayed appearance in the accessory olfactory bulb suggests that VNO(240) is involved in the functional maturation of VNO neurones rather than in axon growth and targeting to the bulb. During the first 2 postnatal weeks, the population of neurones expressing VNO(240) spread peripherally, and by adulthood all primary sensory neurones in the VNO appeared to be expressing this molecule. Similar patterns of expression were also observed for NOC-1, a previously characterized glycoform of the neural cell adhesion molecule NCAM. To date, differential expression of VNO-specific molecules has only been reported along the rostrocaudal axis or at different apical-basal levels in the neuroepithelium. This is the first demonstration of a centroperipheral wave of expression of molecules in the VNO. These results indicate that mechanisms controlling the molecular differentiation of VNO neurones must involve spatial cues organised, not only about orthogonal axes, but also about a centroperipheral axis. Moreover, expression about this centroperipheral axis also involves a temporal component because the subpopulation of neurones expressing VNO(240) and NOC-1 increases during postnatal maturation.
主嗅觉系统和副嗅觉系统在解剖学和功能上都是不同的化学感觉系统。副嗅觉系统的初级感觉神经元聚集在犁鼻器(VNO)中,在那里它们表达信息素受体,这些受体与主要鼻腔中表达的气味受体无关。我们鉴定出一种240 kDa的糖蛋白(VNO(240)),它在小鼠的犁鼻器感觉神经元中选择性表达,而在主嗅觉神经上皮中不表达。VNO(240)在胚胎第20.5天首次由位于新月形犁鼻器中央区域的一小部分感觉神经元表达。尽管在这个年龄在神经元胞体中检测到了VNO(240),但直到出生后第3.5天在副嗅球的轴突中才观察到它。在副嗅球中这种延迟出现表明VNO(240)参与犁鼻器神经元的功能成熟,而不是轴突生长和向嗅球的靶向。在出生后的前两周,表达VNO(240)的神经元群体向周边扩散,到成年时,犁鼻器中的所有初级感觉神经元似乎都在表达这种分子。对于NOC-1(一种先前表征的神经细胞粘附分子NCAM的糖型)也观察到了类似的表达模式。迄今为止,仅报道了犁鼻器特异性分子沿前后轴或神经上皮中不同的顶-基水平的差异表达。这是首次证明犁鼻器中分子表达的中央-外周波。这些结果表明,控制犁鼻器神经元分子分化的机制必须涉及不仅围绕正交轴而且围绕中央-外周轴组织的空间线索。此外,围绕这个中央-外周轴的表达还涉及一个时间成分,因为表达VNO(240)和NOC-1的神经元亚群在出生后成熟过程中增加。