Zhao Shanting, Chai Xuejun, Bock Hans H, Brunne Bianka, Förster Eckart, Frotscher Michael
Institut für Anatomie und Zellbiologie, Albert-Ludwigs-Universität Freiburg, D-79104 Freiburg, Germany.
J Comp Neurol. 2006 Mar 1;495(1):1-9. doi: 10.1002/cne.20846.
Reelin is a positional signal for the lamination of the dentate gyrus. In the reeler mutant lacking Reelin, granule cells are scattered all over the dentate gyrus. We have recently shown that the reeler phenotype of the dentate gyrus can be rescued in vitro by coculturing reeler hippocampal slices with slices from wild-type hippocampus. Here we studied whether Reelin from other brain regions can similarly induce this rescue effect and whether it is mediated via the Reelin receptors apolipoprotein E receptor 2 (ApoER2) and very-low-density lipoprotein receptor (VLDLR). We found that coculturing reeler hippocampal slices with slices from wild-type olfactory bulb, cerebellum, and neocortex rescued the reeler phenotype as seen before with hippocampal slices, provided that the Reelin-synthesizing cells of these regions were placed near the marginal zone of the reeler hippocampal slice. However, coculturing wild-type hippocampal slices with hippocampal slices from mutants deficient in ApoER2 and VLDLR did not rescue the reeler-like phenotype in these cultures. Similarly, no rescue of the reeler-like phenotype was observed in slices from mutants lacking Disabled 1 (Dab1), an adapter protein downstream of Reelin receptors. Conversely, reeler hippocampal slices were rescued by coculturing them with slices from Dab1(-/-) mutants or ApoER2(-/-)/VLDLR(-/-) mice. These findings show that Reelin from other brain regions can substitute for the loss of hippocampal Reelin and that rescue of the reeler phenotype observed in our coculture studies is mediated via lipoprotein receptors for Reelin and Dab1.
Reelin是齿状回分层的位置信号。在缺乏Reelin的reeler突变体中,颗粒细胞散布于整个齿状回。我们最近发现,通过将reeler海马切片与野生型海马切片共培养,齿状回的reeler表型在体外可得到挽救。在此,我们研究了来自其他脑区的Reelin是否能同样诱导这种挽救效应,以及它是否通过Reelin受体载脂蛋白E受体2(ApoER2)和极低密度脂蛋白受体(VLDLR)介导。我们发现,将reeler海马切片与来自野生型嗅球、小脑和新皮质的切片共培养,如同之前与海马切片共培养一样,挽救了reeler表型,前提是这些区域的Reelin合成细胞被放置在reeler海马切片的边缘区附近。然而,将野生型海马切片与缺乏ApoER2和VLDLR的突变体的海马切片共培养,并不能挽救这些培养物中的类reeler表型。同样,在缺乏Disabled 1(Dab1)(一种Reelin受体下游的衔接蛋白)的突变体切片中,未观察到类reeler表型的挽救。相反,将reeler海马切片与来自Dab1(-/-)突变体或ApoER2(-/-)/VLDLR(-/-)小鼠的切片共培养,可使其得到挽救。这些发现表明,来自其他脑区的Reelin可以替代海马Reelin的缺失,并且我们在共培养研究中观察到的reeler表型的挽救是通过Reelin的脂蛋白受体和Dab1介导的。