Joo Kyeung Min, Chung Yoon Hee, Kim Min Kyu, Nam Ryoung Hee, Lee Byung Lan, Lee Kyung Hoon, Cha Choong Ik
Department of Anatomy, Seoul National University College of Medicine, Seoul 110-799, Korea.
J Comp Neurol. 2004 Aug 30;476(4):388-413. doi: 10.1002/cne.20231.
To examine the distributions of VIP/PACAP receptors (VPAC1, VPAC2, and PAC1 receptors) in the brain and to identify the cell types that express these receptors, we performed immunohistochemistry and double immunofluorescence in the rat brain with specific antibodies. The immunohistochemistry revealed that the receptors had distinctive, complementary, and overlapping distribution patterns. High levels of the VPAC1 receptor were expressed in the cerebral cortex, hippocampal formation, deep cerebellar nuclei, thalamus, hypothalamus, and brainstem. The VPAC2 receptors were concentrated in the cerebral cortex, hippocampal formation, amygdalar regions, cerebellar cortex, deep cerebellar nuclei, hypothalamus, and brainstem. On the other hand, the PAC1 receptors had a more restricted distribution pattern in the brain, and high levels of the PAC1 receptors were confined to the cerebellar cortex, deep cerebellar nuclei, epithalamus, hypothalamus, brainstem, and white matter of many brain regions. Also, many fibers expressing the PAC1 receptors were observed in various areas, i.e., the thalamus, hypothalamus, and brainstem. The double immunofluorescence showed that the VIP/PACAP receptors were confined to the neuroglia as well as the neurons. All three types of the VIP/PACAP receptors were expressed in the astrocytes, and the PAC1 receptors were also expressed in the oligodendrocytes. These findings indicate that VIP and PACAP exert their functions through their receptors in specific locations in different combinations. We hope that this first demonstration of the distributions of the VIP/PACAP receptors provides data useful in the investigation of the mechanisms of the many functions of VIP and PACAP in the brain, which require further elucidation.
为了研究血管活性肠肽/垂体腺苷酸环化酶激活肽受体(VPAC1、VPAC2和PAC1受体)在大脑中的分布,并确定表达这些受体的细胞类型,我们用特异性抗体在大鼠脑中进行了免疫组织化学和双重免疫荧光实验。免疫组织化学显示,这些受体具有独特、互补和重叠的分布模式。VPAC1受体在大脑皮质、海马结构、小脑深部核团、丘脑、下丘脑和脑干中高表达。VPAC2受体集中在大脑皮质、海马结构、杏仁核区域、小脑皮质、小脑深部核团、下丘脑和脑干。另一方面,PAC1受体在大脑中的分布模式更为局限,PAC1受体的高表达局限于小脑皮质、小脑深部核团、上丘脑、下丘脑、脑干以及许多脑区的白质。此外,在丘脑、下丘脑和脑干等不同区域观察到许多表达PAC1受体的纤维。双重免疫荧光显示,血管活性肠肽/垂体腺苷酸环化酶激活肽受体局限于神经胶质细胞和神经元。所有三种类型的血管活性肠肽/垂体腺苷酸环化酶激活肽受体均在星形胶质细胞中表达,PAC1受体也在少突胶质细胞中表达。这些发现表明,血管活性肠肽和垂体腺苷酸环化酶激活肽通过其受体在不同位置以不同组合发挥作用。我们希望首次展示的血管活性肠肽/垂体腺苷酸环化酶激活肽受体分布情况能为研究血管活性肠肽和垂体腺苷酸环化酶激活肽在大脑中多种功能的机制提供有用数据,这有待进一步阐明。