Kritzer M F, Innis R B, Goldman-Rakic P S
Section of Neuroanatomy, Yale University School of Medicine, New Haven, Connecticut 06510.
J Comp Neurol. 1987 Sep 15;263(3):418-35. doi: 10.1002/cne.902630308.
Cholecystokinin (CCK) is a putative peptide neurotransmitter present in high concentration in the cerebral cortex. By using techniques of in vitro receptor autoradiography, CCK binding sites in primate cortex were labeled with 125I-Bolton-Hunter-labeled CCK-33 (the 33-amino-acid C-terminal peptide) and 3H-CCK-8 (the C-terminal octapeptide). Biochemical studies performed on homogenized and slide-mounted tissue sections showed that the two ligands labeled a high-affinity, apparently single, saturable site. Autoradiography revealed that binding sites labeled by both ligands were anatomically indistinguishable and were distributed in two basic patterns. A faint and diffuse label characterized portions of medial prefrontal cortex, premotor and motor cortices, the superior parietal lobule, and the temporal pole. In other cortical areas the pattern of binding was layer-specific; i.e., binding sites were concentrated within particular cortical layers and were superimposed upon the background of diffuse label. Layer-specific label was found in the prefrontal cortex, anterior and posterior cingulate gyrus, somatosensory cortex, inferior parietal lobule, retrosplenial cortex, insula, temporal lobe cortices, and in the primary visual and adjacent visual association cortices. The areal and laminar localization of layer-specific CCK binding sites consistently coincided with the cortical projections of thalamic nuclei. In prefrontal cortex, CCK binding sites were present in layers III and IV, precisely paralleling the terminal fields of thalamocortical projections from the mediodorsal and medial pulvinar nucleus of the thalamus. In somatosensory cortex, the pattern of CCK binding in layer IV coincided with thalamic inputs arising from the ventrobasal complex, while in the posterior cingulate gyrus, insular cortex, and retrosplenial cortex, layer IV and lower III binding mirrored the laminar distribution of cortical afferents of the medial pulvinar. CCK binding in layers IVa, IVc alpha, IVc beta, and VI of primary visual cortex corresponded to the terminal field disposition of lateral geniculate neurons, whereas in adjacent visual association cortex, binding in layers III, IV, and VI faithfully followed the cortical distribution of projections from the inferior and lateral divisions of the pulvinar nucleus of the thalamus. We interpret the diffusely labeled binding sites in primate cortex as being associated with the intrinsic system of CCK-containing interneurons that are distributed throughout all layers and areas of the cortex. The stratified binding sites, however, appear to be associated with specific extrinsic peptidergic projections.(ABSTRACT TRUNCATED AT 400 WORDS)
胆囊收缩素(CCK)是一种假定的肽类神经递质,在大脑皮层中含量很高。通过体外受体放射自显影技术,用125I-博尔顿-亨特标记的CCK-33(33个氨基酸的C末端肽)和3H-CCK-8(C末端八肽)标记灵长类动物皮层中的CCK结合位点。对匀浆和载玻片上的组织切片进行的生化研究表明,这两种配体标记了一个高亲和力、明显单一、可饱和的位点。放射自显影显示,两种配体标记的结合位点在解剖学上无法区分,且分布有两种基本模式。内侧前额叶皮层、运动前区和运动皮层、顶上小叶和颞极的部分区域有微弱而弥散的标记。在其他皮层区域,结合模式具有层特异性;即结合位点集中在特定的皮层层内,并叠加在弥散标记的背景上。在额叶前皮质、前扣带回和后扣带回、躯体感觉皮层、顶下小叶、压后皮质、脑岛、颞叶皮层以及初级视觉和相邻视觉联合皮层中发现了层特异性标记。层特异性CCK结合位点的区域和层定位始终与丘脑核的皮层投射一致。在额叶前皮质中,CCK结合位点存在于III层和IV层,与来自丘脑背内侧核和内侧枕核的丘脑皮质投射的终末场精确平行。在躯体感觉皮层中,IV层的CCK结合模式与来自腹后复合体的丘脑输入一致,而在扣带回后部、脑岛皮层和压后皮质中,IV层和III层下部的结合反映了内侧枕核皮层传入纤维的层分布。初级视觉皮层IVa、IVcα、IVcβ和VI层中的CCK结合对应于外侧膝状神经元的终末场分布,而在相邻的视觉联合皮层中,III、IV和VI层中的结合忠实地遵循丘脑枕核下部和外侧部投射的皮层分布。我们将灵长类动物皮层中弥散标记的结合位点解释为与分布在皮层所有层和区域的含CCK中间神经元的内在系统相关。然而,分层的结合位点似乎与特定的外在肽能投射相关。(摘要截取自400字)