Del Turco Domenico, Gebhardt Carl, Burbach Guido J, Pleasure Samuel J, Lowenstein Daniel H, Deller Thomas
Department of Clinical Neuroanatomy, J.W. Goethe University, D-60590 Frankfurt/Main, Germany.
J Comp Neurol. 2004 Sep 6;477(1):81-95. doi: 10.1002/cne.20239.
The dentate gyrus of rodents is characterized by a highly laminar organization: above a compact granule cell layer, commissural/associational (C/A) fibers terminate on proximal granule cell dendrites and entorhinal fibers terminate on distal granule cell dendrites in a nonoverlapping manner. To gain insights into mechanisms that underlie the formation of this laminar structure, we studied mice deficient for BETA2/NeuroD, a basic helix-loop-helix transcription factor essential for granule cell differentiation. Anterograde tracing was used to label C/A and entorhinal fibers and combined with confocal double immunofluorescence for calbindin, calretinin, parvalbumin, and reelin to visualize putative target cells. The dentate gyrus of mutant mice contained only few granule cells, which formed a cap-like structure adjacent to area CA3. Despite the severe hypoplasia of the dentate gyrus, the remaining BETA2/NeuroD-deficient granule cells expressed mature markers, extended dendrites into the molecular layer, and extended mossy fibers into area CA3. Entorhinal and C/A fibers terminated in a nonoverlapping manner in the dendritic field overlying the rudiment. Entorhinal fibers terminated in the outermost portion of the dentate gyrus where they surrounded reelin-positive Cajal-Retzius cells, and C/A fibers terminated above and within the dentate rudiment. The laminar termination of C/A fibers was closest to normal in zones of the rudiment in which granule cells were densely packed. These data indicate that granule cells are able to differentiate in the absence of BETA2/NeuroD and suggest that the signals underlying the laminar anatomy of the dentate gyrus are present in the absence of most target cells.
在紧密的颗粒细胞层上方,连合/联合(C/A)纤维以不重叠的方式终止于近端颗粒细胞树突,而内嗅纤维则终止于远端颗粒细胞树突。为了深入了解这种分层结构形成的潜在机制,我们研究了缺乏BETA2/NeuroD的小鼠,BETA2/NeuroD是颗粒细胞分化所必需的一种碱性螺旋-环-螺旋转录因子。采用顺行示踪法标记C/A纤维和内嗅纤维,并结合钙结合蛋白、钙视网膜蛋白、小白蛋白和Reelin的共聚焦双免疫荧光,以可视化假定的靶细胞。突变小鼠的齿状回仅含有少量颗粒细胞,这些颗粒细胞在CA3区附近形成帽状结构。尽管齿状回严重发育不全,但剩余的缺乏BETA2/NeuroD的颗粒细胞表达成熟标记物,树突延伸至分子层,并将苔藓纤维延伸至CA3区。内嗅纤维和C/A纤维在覆盖残基的树突区域以不重叠的方式终止。内嗅纤维在齿状回的最外层终止,在那里它们围绕着Reelin阳性的Cajal-Retzius细胞,而C/A纤维在齿状残基上方和内部终止。在颗粒细胞密集堆积的残基区域,C/A纤维的分层终止最接近正常。这些数据表明,在缺乏BETA2/NeuroD的情况下颗粒细胞仍能够分化,并表明在大多数靶细胞缺失的情况下,齿状回分层解剖结构的潜在信号依然存在。