Doucette R
Department of Anatomy and Cell Biology, College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Int J Dev Neurosci. 1996 Nov;14(7-8):945-59. doi: 10.1016/s0736-5748(96)00042-1.
When the olfactory nerve is injured in adult mammals, the axons grow across the PNS-CNS transitional zone and re-innervate their synaptic contacts within the olfactory bulb. Some years ago, Liesi [Liesi P. (1985) Laminin-immunoreactive glia distinguish regenerative adult CNS systems from non-regenerative ones. EMBO J. 4, 2505-2511] reported the presence of laminin in non-basal lamina locations within the nerve fiber layer (NFL) of the olfactory bulb of adult rats and suggested that this molecule may facilitate olfactory axonal growth into and within the CNS. The purpose of the present study was to compare the expression of laminin, fibronectin, and collagen type IV in: (a) the NFL of developing and adult rats; and (b) the NFL rostral and caudal to a stab wound in the olfactory bulb of adult rats. Numerous punctate deposits of immunofluorescence were seen in the NFL of the E18 (Theiler stage 23) bulb when antisera to laminin, fibronectin or collagen type IV were used. There was a dramatic drop-off in staining at the border between the NFL and the presumptive glomerular layer. The staining pattern was similar in the newborn bulb, although the immunofluorescence was not as strong. In the unoperated adult rats, only laminin was present consistently as punctate deposits within the NFL, whereas all three antisera stained numerous punctate deposits within the NFL during the first week after a stab wound. Although there was a partial recapitulation of the expression pattern for laminin, fibronectin and collagen type IV in the lesioned adult NFL, it never reached the extent found in the E18 or newborn bulbs and its expression returned to normal levels prior to the re-innervation of the bulb during the second and third weeks after surgery. The results suggest that the molecular requirements for the successful growth of olfactory axons may differ during development to growth in adult animals.
在成年哺乳动物中,当嗅神经受损时,轴突会穿过外周神经系统 - 中枢神经系统过渡区,并重新支配它们在嗅球内的突触连接。几年前,莱西[莱西P.(1985年)层粘连蛋白免疫反应性神经胶质细胞区分再生的成年中枢神经系统系统和非再生系统。《欧洲分子生物学组织杂志》4,2505 - 2511]报道成年大鼠嗅球神经纤维层(NFL)非基底层位置存在层粘连蛋白,并表明该分子可能促进嗅轴突向中枢神经系统内生长及在中枢神经系统内的生长。本研究的目的是比较层粘连蛋白、纤连蛋白和IV型胶原在以下方面的表达:(a)发育中和成年大鼠的NFL;以及(b)成年大鼠嗅球刺伤伤口头侧和尾侧的NFL。当使用针对层粘连蛋白、纤连蛋白或IV型胶原的抗血清时,在E18(泰勒阶段23)嗅球的NFL中可见大量点状免疫荧光沉积物。在NFL与假定的肾小球层之间的边界处染色急剧下降。新生嗅球的染色模式相似,尽管免疫荧光没有那么强。在未手术的成年大鼠中,只有层粘连蛋白始终以点状沉积物的形式存在于NFL内,而在刺伤后的第一周内,所有三种抗血清都在NFL内染出大量点状沉积物。尽管在受损的成年NFL中层粘连蛋白、纤连蛋白和IV型胶原的表达模式有部分重现,但从未达到在E18或新生嗅球中发现的程度,并且在手术后第二和第三周嗅球重新支配之前其表达恢复到正常水平。结果表明,嗅轴突成功生长的分子需求在发育过程与成年动物生长过程中可能有所不同。