Czarnecki Kathrin, Haas Carola A, Bas Orth Carlos, Deller Thomas, Frotscher Michael
Institute of Anatomy and Cell Biology, Albert-Ludwigs-Universität Freiburg, D-79104 Freiburg, Germany.
J Comp Neurol. 2005 Sep 19;490(2):133-44. doi: 10.1002/cne.20651.
Synaptopodin is an actin-binding protein of renal podocytes and dendritic spines. We have recently shown that synaptopodin is localized to the spine apparatus, a characteristic organelle of dendritic spines on forebrain neurons. Synaptopodin-deficient mice do not form spine apparatuses, indicating a role of synaptopodin in the formation of this organelle. Here we studied the development of synaptopodin expression in the postnatal rat hippocampus. At birth, synaptopodin mRNA is mainly expressed in CA3 pyramidal neurons. At postnatal day (P) 6, synaptopodin mRNA expression is still strongest in CA3 but is now also found in CA1 pyramidal neurons and granule cells of the suprapyramidal blade of the dentate gyrus. At P9, an almost adult pattern is seen with synaptopodin mRNA expressed by virtually all principal neurons. While synaptopodin mRNA was restricted to cell somata, immunostaining for synaptopodin protein labeled dendritic layers. At birth, no immunoreactivity was visible, while at P5 a weak staining mainly in stratum oriens was observed. At P9, immunolabeling was still strongest in stratum oriens followed by the molecular layer of the dentate gyrus. The adult pattern with strong labeling of all dendritic layers was reached by P12. Together these findings show that synaptopodin expression follows the well-known sequence of hippocampal principal neuron development. Unexpectedly, we also observed synaptopodin mRNA expression in a small population of interneurons as revealed by double labeling with interneuron markers. However, no immunolabeling for synaptopodin was observed in identified interneurons, confirming that the protein is mainly present in spine-bearing principal cells.
突触足蛋白是肾足细胞和树突棘中的一种肌动蛋白结合蛋白。我们最近发现,突触足蛋白定位于棘器,这是前脑神经元树突棘的一种特征性细胞器。缺乏突触足蛋白的小鼠不会形成棘器,这表明突触足蛋白在该细胞器的形成中起作用。在此,我们研究了出生后大鼠海马体中突触足蛋白表达的发育情况。出生时,突触足蛋白mRNA主要在CA3锥体神经元中表达。在出生后第(P)6天,突触足蛋白mRNA表达仍在CA3中最强,但现在也在CA1锥体神经元和齿状回上颗粒层的颗粒细胞中发现。在P9时,几乎呈现成年模式,几乎所有主要神经元都表达突触足蛋白mRNA。虽然突触足蛋白mRNA局限于细胞体,但突触足蛋白的免疫染色标记了树突层。出生时,未见免疫反应性,而在P5时,主要在海马下托观察到弱阳性染色。在P9时,免疫标记在海马下托中仍然最强,其次是齿状回的分子层。到P12时达到所有树突层都有强标记的成年模式。这些发现共同表明,突触足蛋白的表达遵循海马主要神经元发育的众所周知的顺序。出乎意料的是,我们还通过与中间神经元标记物的双重标记发现,在一小部分中间神经元中观察到突触足蛋白mRNA表达。然而,在已鉴定的中间神经元中未观察到突触足蛋白的免疫标记,证实该蛋白主要存在于带有树突棘的主要细胞中。