Wüllner U, Isenmann S, Gleichmann M, Klockgether T, Bähr M
Department of Neurology, Eberhard-Karls-University, Hoppe-Seyler-Str. 3, D-72076 Tübingen, Germany.
Brain Res Dev Brain Res. 1998 Sep 10;110(1):1-6. doi: 10.1016/s0165-3806(98)00079-0.
To test the hypothesis whether a failure to express neurotrophins or a neurotrophin receptor might underlie the pathology observed in mutant mice with degeneration of regionally distinct subpopulations of neurons, the expression of BDNF, NT-3, TrkB, TrkC and synaptophysin mRNA was examined in the cerebellum of mutant lurcher (lc/+) and weaver (wv/+)/(wv/wv) mice. To identify the expression patterns of individual neurons, we used in situ hybridization with digoxigenin labeled ribonucleotide probes. RT-PCR of cerebellar mRNA for BDNF, NT-3, TrkB and TrkC (GAPDH as internal standard) was performed in parallel. Although especially in homozygous (wv/wv) weaver mice the normal anatomical order and number of the cerebellar neurons is grossly disturbed, residual Purkinje and granule neurons of both mutants displayed a normal expression pattern of the neurotrophins examined. Thus, the affected animals showed no significant signal decrease compared to healthy littermates or C3H mice. Our results suggest that the loss of specific neuron populations in the cerebellum of either mutant occurs via mechanisms either independent or downstream of the neurotrophins examined in this study.
为了验证神经营养因子或神经营养因子受体表达缺失是否可能是导致具有区域特异性神经元亚群退化的突变小鼠所观察到的病理现象的原因,我们检测了突变型蹒跚(lc/+)和织工(wv/+)/(wv/wv)小鼠小脑内脑源性神经营养因子(BDNF)、神经营养因子-3(NT-3)、酪氨酸激酶受体B(TrkB)、酪氨酸激酶受体C(TrkC)和突触素mRNA的表达。为了确定单个神经元的表达模式,我们使用了地高辛标记的核糖核苷酸探针进行原位杂交。同时进行了小脑mRNA中BDNF、NT-3、TrkB和TrkC的逆转录聚合酶链反应(RT-PCR)(以甘油醛-3-磷酸脱氢酶(GAPDH)作为内参)。尽管特别是在纯合(wv/wv)织工小鼠中,小脑神经元的正常解剖结构和数量受到严重干扰,但两种突变体残留的浦肯野神经元和颗粒神经元在所检测的神经营养因子方面均表现出正常的表达模式。因此,与健康同窝小鼠或C3H小鼠相比,患病动物未显示出明显的信号降低。我们的结果表明,这两种突变体小鼠小脑中特定神经元群体的丧失是通过独立于或在本研究中检测的神经营养因子下游的机制发生的。