首页> 外文期刊>Regulatory peptides. >Expression of pituitary adenylate cyclase activating peptide (PACAP) and PACAP type I receptors in the rat adrenal medulla.
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Expression of pituitary adenylate cyclase activating peptide (PACAP) and PACAP type I receptors in the rat adrenal medulla.

机译:垂体腺苷酸环化酶激活肽(PACAP)和PACAP I型受体在大鼠肾上腺髓质中的表达。

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Pituitary adenylate cyclase activating polypeptide (PACAP) which belongs to the vasoactive intestinal polypeptide family of regulatory peptides, occurs in two variants, PACAP-27 and PACAP-38, and is thought to be an important messenger in both the central and peripheral nervous system. Three cloned G-protein coupled 7 transmembrane spanning receptors bind PACAP with high affinity, one reacting only weakly with VIP (PACAP type I receptor) the other two binding vasoactive intestinal peptide (VIP) with equally high affinity (VIP type I and II receptors). The PACAP type I receptor displays high affinity for both variants of PACAP. In this study, we have investigated the distribution of PACAP and the PACAP type I receptor in the adrenal medulla of newborn and adult rat. Immunocytochemistry revealed, in the adult rat, a dense network of PACAP-immunoreactive nerve fibers terminating on chromaffin cells. Such fibers were few and weakly immunoreactive in the newborn rat. PACAP-immunoreactive medullary cells could not be detected in the adult rat, whereas in the newborn, occasional cells were seen. By in situ-hybridization we detected PACAP type I receptor mRNA in a majority of the adrenal medullary cells of both newborn and adult rat. Receptor autoradiography using 125I-PACAP-27 as ligand revealed binding-sites with a localization virtually identical to the in situ hybridization signal indicating a functional expression of high-affinity type I PACAP receptors in the adrenal medulla. Additionally, in the adult rat, single or clustered large cells, presumably ganglion cells, contained an even higher abundance of PACAP receptor mRNA as well as binding sites than the surrounding chromaffin cells. Our observations on the distribution of PACAP peptide and PACAP receptors in the adrenal medulla suggest that both chromaffin cells and ganglion cells are PACAP targets. The data thus strengthen earlier observations indicating an important regulatory role of PACAP in catecholamine biosynthesis and release. The presence of both ligand and receptors in newborn rats may indicate a role for PACAP in the development of the adrenal medulla.
机译:垂体腺苷酸环化酶激活多肽(PACAP)属于血管活性肠多肽调节肽家族,以两种变体出现,即PACAP-27和PACAP-38,并且被认为是中枢和外周神经系统的重要信使。三个克隆的G蛋白偶联的7个跨膜跨越受体以高亲和力结合PACAP,一个仅与VIP(PACAP I型受体)微弱反应,另外两个以同样高亲和力(VIP I和II型受体)结合血管活性肠肽(VIP)。 。 PACAP I型受体对两种PACAP变体均显示出高亲和力。在这项研究中,我们调查了新生大鼠和成年大鼠肾上腺髓质中PACAP和I型PACAP受体的分布。免疫细胞化学显示,在成年大鼠中,PACAP免疫反应性神经纤维的密集网络终止于嗜铬细胞。这样的纤维很少,并且在新生大鼠中免疫反应性弱。在成年大鼠中未检测到PACAP免疫反应性髓样细胞,而在新生大鼠中偶尔可见到细胞。通过原位杂交,我们在新生和成年大鼠的大多数肾上腺髓质细胞中检测到了PACAP I型受体mRNA。使用125 I-PACAP-27作为配体的受体放射自显影显示结合位点,其定位与原位杂交信号基本相同,表明肾上腺髓质中高亲和力I型PACAP受体的功能性表达。另外,在成年大鼠中,单个或成簇的大细胞(可能是神经节细胞)比周围的嗜铬细胞包含更高的PACAP受体mRNA丰度和结合位点。我们对肾上腺髓质中PACAP肽和PACAP受体分布的观察表明,嗜铬细胞和神经节细胞都是PACAP的靶标。因此,这些数据加强了先前的观察结果,表明PACAP在儿茶酚胺生物合成和释放中具有重要的调节作用。新生大鼠体内配体和受体的存在可能表明PACAP在肾上腺髓质的发育中发挥了作用。

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