Muma N A, Slunt H H, Hoffman P N
Department of Pathology, Johns Hopkins University, Baltimore, Maryland 21205.
J Neurocytol. 1991 Oct;20(10):844-54. doi: 10.1007/BF01191735.
Neurofilament gene expression appears to play an important role in regulating axonal calibre. In the dorsal root ganglia of mature mammals, large sensory neurons contain high levels of neurofilament mRNAs and give rise to large-calibre myelinated axons (with diameters up to 8 microns in rat), while small sensory neurons contain undetectable levels of neurofilament mRNAs and give rise to unmyelinated axons (with diameters less than 1 micron). In the present study we used a combination of morphological and molecular approaches to examine the relationships among postnatal increases in neurofilament gene expression, growth in perikaryal size, growth in axonal calibre and myelin formation in lumbar sensory neurons of rat. Using in situ hybridization, three populations of sensory neurons could be clearly distinguished at birth: (1) neurons containing relatively high levels of neurofilament mRNAs; (2) neurons containing low levels of neurofilament mRNAs; and (3) neurons containing undetectable levels of neurofilament mRNAs. Perikaryal size was greater for neurons with high levels of neurofilament mRNAs than for those with either low or undetectable levels. The proportion of neurons expressing high levels of neurofilament mRNAs increased from approximately 10% at birth to 30% by 28 days of age; increases in the abundance of neurofilament mRNAs in these neurons between 0 and 28 days of age, as documented by blot analyses of RNA purified from dorsal root ganglia, correlated with increases in perikaryal size. This postnatal rise in neurofilament gene expression also correlated with an increase in the cross-sectional areas of myelinated axons in the L5 dorsal root. As axons matured in their relationship to Schwann cells (polyaxonal pockets----ensheathed----segregated----myelinated), their cross-sectional areas increased. Thus, growth in both perikaryal size and axonal calibre correlated closely with increased neurofilament gene expression in these sensory neurons. These findings are consistent with the hypothesis that neurofilament expression plays an important role in the sequence of events leading to the radial growth and myelination of axons.
神经丝基因表达似乎在调节轴突直径方面发挥着重要作用。在成熟哺乳动物的背根神经节中,大型感觉神经元含有高水平的神经丝mRNA,并产生大直径的有髓轴突(大鼠中直径可达8微米),而小型感觉神经元含有无法检测到的神经丝mRNA水平,并产生无髓轴突(直径小于1微米)。在本研究中,我们使用形态学和分子方法相结合的方式,来研究大鼠腰段感觉神经元中神经丝基因表达的出生后增加、胞体大小的增长、轴突直径的增长以及髓鞘形成之间的关系。通过原位杂交,在出生时可以清楚地区分出三类感觉神经元:(1)含有相对高水平神经丝mRNA的神经元;(2)含有低水平神经丝mRNA的神经元;(3)含有无法检测到的神经丝mRNA水平的神经元。神经丝mRNA水平高的神经元的胞体大小,比那些水平低或无法检测到的神经元更大。表达高水平神经丝mRNA的神经元比例从出生时的约10%增加到28日龄时的30%;从背根神经节纯化的RNA的印迹分析记录显示,这些神经元在0至28日龄之间神经丝mRNA丰度的增加,与胞体大小的增加相关。神经丝基因表达的这种出生后升高,也与L5背根中有髓轴突横截面积的增加相关。随着轴突在与施万细胞的关系中成熟(多轴突囊——被包裹——分离——有髓),它们的横截面积增加。因此,这些感觉神经元中胞体大小和轴突直径的增长,都与神经丝基因表达的增加密切相关。这些发现与以下假设一致,即神经丝表达在导致轴突径向生长和髓鞘形成的一系列事件中起重要作用。