Jinno S, Kinukawa N, Kosaka T
Department of Anatomy and Neurobiology, Graduate School of Medical Sciences, Kyushu University, Higashi-ku, 812-8582, Fukuoka, Japan.
Brain Res. 2001 May 11;900(2):195-204. doi: 10.1016/s0006-8993(01)02292-2.
Several studies reported the morphology of calretinin-positive (CR+) neurons and nicotinamide adenine dinucleotide phosphate diaphorase (NADPH-d) labeled or neuronal nitric oxide synthase-positive (nNOS+) neurons in the rodent hippocampus, where these neurons showed similar morphological features. In addition, a previous study reported the frequent colocalization of CR and NADPH-d in the rat hippocampus. In this study, we aimed to examine whether CR+ neurons and nNOS+ neurons belong to a same morphological subpopulation of GABAergic neurons in the mouse hippocampus. Neurons were immunocytochemically classified into three groups, i.e., CR+/nNOS-, CR-/nNOS+ and CR+/nNOS+ groups. The present morphometric analysis was performed in the mouse Ammon's horn, because CR+/nNOS+ neurons were rarely found in the mouse dentate gyrus. We selected three morphometric parameters, i.e., soma area, soma form factor (FF) and number of primary dendrites. Dunnett's post-hoc analysis revealed that soma area, soma FF and number of primary dendrites were significantly larger in CR-/nNOS+ group than in CR+/nNOS- and CR+/nNOS+ groups. The morphometric data of CR+/nNOS+ group were quite similar to those of CR+/nNOS- group. The morphometric multivariate logistic regression analysis revealed that these three morphometric parameters were independent significant variables to discriminate between CR+/nNOS- and CR-/nNOS+ groups, and the majority of CR+/nNOS- and CR-/nNOS+ groups were correctly classified from the morphometric features. The present results clearly indicate that CR+/nNOS- neurons and CR-/nNOS+ neurons belong to different morphological subpopulations, and lead us to speculate that they might play different functional roles in the hippocampal circuit. The further application of morphometric multivariate analysis would be valuable to understand the functional roles of chemically defined neurons in the various brain regions.
多项研究报道了啮齿动物海马体中钙视网膜蛋白阳性(CR+)神经元以及烟酰胺腺嘌呤二核苷酸磷酸黄递酶(NADPH-d)标记的或神经元型一氧化氮合酶阳性(nNOS+)神经元的形态,这些神经元呈现出相似的形态特征。此外,先前的一项研究报道了大鼠海马体中CR与NADPH-d的频繁共定位。在本研究中,我们旨在研究CR+神经元和nNOS+神经元是否属于小鼠海马体中GABA能神经元的同一形态亚群。通过免疫细胞化学方法将神经元分为三组,即CR+/nNOS-组、CR-/nNOS+组和CR+/nNOS+组。由于在小鼠齿状回中很少发现CR+/nNOS+神经元,因此本形态计量分析在小鼠海马结构进行。我们选择了三个形态计量参数,即胞体面积、胞体形态因子(FF)和初级树突数量。Dunnett事后分析显示,CR-/nNOS+组的胞体面积、胞体FF和初级树突数量显著大于CR+/nNOS-组和CR+/nNOS+组。CR+/nNOS+组的形态计量数据与CR+/nNOS-组非常相似。形态计量多变量逻辑回归分析显示,这三个形态计量参数是区分CR+/nNOS-组和CR-/nNOS+组的独立显著变量,并且根据形态特征能够正确分类大多数CR+/nNOS-组和CR-/nNOS+组。目前的结果清楚地表明,CR+/nNOS-神经元和CR-/nNOS+神经元属于不同的形态亚群,这使我们推测它们可能在海马回路中发挥不同的功能作用。形态计量多变量分析的进一步应用对于理解化学定义的神经元在各个脑区的功能作用将是有价值的。