Hazell A S, McGahan L, Tetzlaff W, Bedard A M, Robertson G S, Nakabeppu Y, Hakim A M
Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec.
J Mol Neurosci. 1998 Feb;10(1):1-15. doi: 10.1007/BF02737081.
Pyrithiamine-induced thiamine deficiency (PTD) in the rat is associated with neuronal loss in the thalamus and inferior colliculus. Recently, we were able to demonstrate the occurrence of apoptosis in the thalamus of these animals. Given that immediate-early genes (IEGs) participate in signal transduction pathways that mediate programmed cell death, the present study utilized in situ hybridization and immunohistochemistry to examine the expression of four IEGs (c-fos, c-jun, fos-B, and NGFI-A) during the progression of PTD. Elevated c-fos mRNA levels were initially observed in the posterior medial thalamus on d 12 of the deficiency. At the acute symptomatic stage (characterized by a loss of righting reflex on d 16-17), the posterior-medial thalamus exhibited increased mRNA for all genes examined, whereas the inferior colliculus demonstrated mRNA induction for c-fos, c-jun, and NGFI-A. Immunohistochemical analysis revealed that elevations of IEG mRNA associated with the acute symptomatic stage were consistently translated into protein in the thalamus. In contrast, whereas elevated Fos- and Jun-like immunoreactivity were detected in the inferior colliculus at this stage, NGFI-A-like immunoreactivity declined significantly below basal levels, suggesting a translational block. These results are consistent with our recent findings of apoptotic cell death, and indicate that differential patterns of IEG expression occur in the thalamus and inferior colliculus during PTD, which may contribute to the pathogenesis of this disorder.
大鼠中吡硫胺诱导的硫胺素缺乏(PTD)与丘脑和下丘的神经元丢失有关。最近,我们能够证明这些动物丘脑中凋亡的发生。鉴于即刻早期基因(IEGs)参与介导程序性细胞死亡的信号转导途径,本研究利用原位杂交和免疫组织化学来检测PTD进展过程中四种IEGs(c-fos、c-jun、fos-B和NGFI-A)的表达。在缺乏的第12天,最初在丘脑后内侧观察到c-fos mRNA水平升高。在急性症状期(以第16 - 17天翻正反射丧失为特征),丘脑后内侧所有检测基因的mRNA均增加,而下丘c-fos、c-jun和NGFI-A的mRNA出现诱导。免疫组织化学分析显示,与急性症状期相关的IEGs mRNA升高在丘脑中始终翻译为蛋白质。相比之下,虽然此时在下丘检测到Fos样和Jun样免疫反应性升高,但NGFI-A样免疫反应性显著低于基础水平,提示存在翻译阻滞。这些结果与我们最近关于凋亡细胞死亡的发现一致,并表明PTD过程中丘脑和下丘存在IEGs表达的差异模式,这可能有助于该疾病的发病机制。