Mikkelsen J D, Larsen P J, Kruse-Larsen C, O'Hare M M, Schwartz T W
Institute of Medical Anatomy, Department B, Copenhagen, Denmark.
Brain Res Bull. 1993;31(3-4):415-25. doi: 10.1016/0361-9230(93)90235-4.
Proneuropeptide Y (proNPY) is posttranslationally processed to NPY(1-36)amide and the C-terminal flanking peptide of NPY (CPON). Antisera directed against the N-terminal part of NPY, CPON, or CysNPY(32-36)amide were used to identify peptide fragments processed from proNPY in biopsies of human frontal cortical specimens obtained from patients who underwent surgical treatment of profound cerebral tumors. Gel filtration and radioimmunoassays of human cortical extracts revealed that the NPY immunoreactivity was found only as NPY(1-36)amide, indicating that all NPY is present in an amidated form. In contrast, no intact proNPY was identified. NPY/CPON-immunoreactive neurons were observed to be nonspiny with long axonal processes mostly orientated longitudinally in the direction of the superficial layers. Bundles of immunoreactive fibers in the underlying white matter were orientated toward superficial layers of the neocortex, indicating a subcortical origin of some NPY/CPON nerve fibers. Axonal terminals were distributed throughout the neocortex, with highest numbers observed in layer I. Some fibers penetrated from the superficial layer I into the overlying pial surface. Many fibers were also observed in proximity to intracortical blood vessels, and some of these fibers originated from the cortical neurons, indicating that NPY could play a role as an intracortical autoregulator of the tonus of cerebral arterioles. Together these results indicate that NPY(1-36)amide and CPON are present in intracortical neurons as two independent molecules and that NPY may be involved in synaptic processes and regulation of blood flow in the human brain.
前神经肽Y(proNPY)经翻译后加工生成NPY(1-36)酰胺和NPY的C端侧翼肽(CPON)。使用针对NPY的N端部分、CPON或CysNPY(32-36)酰胺的抗血清,来鉴定从接受深部脑肿瘤手术治疗患者的人类额叶皮质标本活检中由proNPY加工而来的肽片段。对人类皮质提取物进行凝胶过滤和放射免疫分析发现,NPY免疫反应性仅以NPY(1-36)酰胺的形式存在,这表明所有NPY均以酰胺化形式存在。相比之下,未鉴定出完整的proNPY。观察到NPY/CPON免疫反应性神经元无棘,具有大多沿浅层纵向排列的长轴突。下层白质中的免疫反应性纤维束朝向新皮质的浅层,表明一些NPY/CPON神经纤维起源于皮质下。轴突终末分布于整个新皮质,在I层数量最多。一些纤维从浅层I层穿透至上覆的软脑膜表面。在皮质内血管附近也观察到许多纤维,其中一些纤维起源于皮质神经元,这表明NPY可能作为脑小动脉张力的皮质内自动调节因子发挥作用。这些结果共同表明,NPY(1-36)酰胺和CPON作为两个独立分子存在于皮质内神经元中,并且NPY可能参与人类大脑中的突触过程和血流调节。