Druga R, Chen S, Bentivoglio M
Institute of Anatomy and Histology, University of Verona, Italy.
J Chem Neuroanat. 1993 Nov-Dec;6(6):399-406. doi: 10.1016/0891-0618(93)90014-u.
The distribution of the calcium binding proteins parvalbumin and calbindin D-28k was examined in the claustrum of the rat by means of immunohistochemistry. The two proteins displayed a different and largely complementary pattern of distribution. Parvalbumin-immunostaining was intense in the neuropil of the dorsal claustrum and virtually absent in the neuropil of the ventral claustrum; parvalbumin-immunoreactive neuronal cell bodies were relatively numerous in the dorsal claustrum and were detected only occasionally in the ventral region. On the other hand, calbindin-immunostaining was prevalent in the ventral claustrum; very few calbindin-positive neurons were seen in the dorsal sector of the nucleus, whereas they were relatively more numerous in the ventral claustrum. The cell bodies of the majority of the claustral parvalbumin- or calbindin-immunoreactive neurons were oval or round, but immunostained polymorphous neurons were also observed. The surface of the immunopositive dendritic branches was smooth, with no evidence of spines. Fluorescent retrograde tracing was combined with immunohistofluorescence to determine whether the parvalbumin-containing claustral cells project to the frontoparietal cortex. Neurons labelled after large fluorogold injections in frontoparietal cortical fields were highly intermingled in the dorsal claustrum with parvalbumin-immunoreactive cells but the two neuronal populations were separate. These data show that parvalbumin-immunoreactive claustral neurons do not project to the frontoparietal cortex. In addition, although these cells may project to other cortical or subcortical targets, the present findings suggest that they may represent, at least in part, local circuit claustral neurons, corresponding to the aspiny intrinsic neurons described in the rat claustrum in studies based on Golgi impregnation.
通过免疫组织化学方法,研究了大鼠屏状核中钙结合蛋白小白蛋白和钙结合蛋白D-28k的分布情况。这两种蛋白呈现出不同且在很大程度上互补的分布模式。小白蛋白免疫染色在背侧屏状核的神经毡中强烈,而在腹侧屏状核的神经毡中几乎不存在;小白蛋白免疫反应性神经元细胞体在背侧屏状核中相对较多,在腹侧区域仅偶尔检测到。另一方面,钙结合蛋白免疫染色在腹侧屏状核中普遍存在;在该核的背侧部分很少见到钙结合蛋白阳性神经元,而在腹侧屏状核中相对较多。大多数屏状核小白蛋白或钙结合蛋白免疫反应性神经元的细胞体呈椭圆形或圆形,但也观察到免疫染色的多形性神经元。免疫阳性树突分支的表面光滑,没有棘的迹象。将荧光逆行追踪与免疫荧光相结合,以确定含小白蛋白的屏状核细胞是否投射到额顶叶皮质。在额顶叶皮质区域进行大剂量荧光金注射后标记的神经元,在背侧屏状核中与小白蛋白免疫反应性细胞高度混合,但这两个神经元群体是分开的。这些数据表明,小白蛋白免疫反应性屏状核神经元不投射到额顶叶皮质。此外,尽管这些细胞可能投射到其他皮质或皮质下靶点,但目前的研究结果表明,它们可能至少部分代表局部回路屏状核神经元,对应于基于高尔基浸染法在大鼠屏状核研究中描述的无棘内在神经元。