肽前体加工酶的神经解剖学和功能研究。

Enzyme Pub Date : 1991-01-01 DOI:10.1159/000468902
W E Cullinan, N C Day, M K Schäfer, R Day, N G Seidah, M Chrétien, H Akil, S J Watson
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引用次数: 21

摘要

本文综述了原位杂交定位研究,比较了编码蛋白转化酶Furin、PC1和PC2的mRNA转录本与编码羧基肽酶H (CPE)和肽基甘氨酸酰胺化单加氧酶(PAM)的mRNA转录本在大脑中的分布。Furin mRNA在所有脑区神经元细胞和非神经元细胞中均检测到。PC1和PC2的细胞定位主要是神经元,PC2的分布普遍更广泛,尽管也发现了许多区域差异。在多肽丰富的脑区检测到转换酶、CPE和PAM的特定组合表明,特定的酶途径参与了神经肽的加工。结果还描述了一系列关于异源神经细胞系neuro2a中前opiomelanocortin (POMC)加工的功能研究,该细胞系表达低水平的PC2 mRNA,但未检测到PC1 mRNA。我们观察到两种截然不同的POMC加工模式:一种是前体在多个裂解位点加工产生多种肽,另一种是POMC在单个裂解位点加工产生β E。如果PC2在转染细胞中负责POMC加工,那么在后一种类型的细胞系中,这种酶可能更倾向于切割氨基末端加工位点,而不是其他位点。
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Neuroanatomical and functional studies of peptide precursor-processing enzymes.

An overview of in situ hybridization mapping studies comparing the brain distributions of mRNA transcripts encoding the proprotein convertase Furin, PC1 and PC2 in relation to transcripts encoding carboxypeptidase H (CPE) and peptidylglycine alpha-amidating monooxygenase (PAM) is presented. Furin mRNA was detected in both neurons and non-neuronal cells throughout all brain areas. The cellular localization of PC1 and PC2 was primarily neuronal, with PC2 generally more widely distributed, although many regional variations were detected. The detection of specific combinations of the convertases, CPE and PAM in peptide-rich brain regions suggests that specific enzymatic pathways are involved in neuropeptide processing. Results are also described from a series of functional studies on the processing of pro-opiomelanocortin (POMC) in a heterologous neuronal cell line, Neuro-2A, which expresses low levels of PC2 mRNA but no detectable PC1 mRNA. Two contrasting POMC-processing patterns were observed: one where the precursor was processed at a number of cleavage sites to produce several peptides, and another where POMC was processed at a single cleavage site to produce beta E only. If PC2 is responsible for POMC processing in transfected cells, this enzyme may have favored cleavage of the amino terminal-processing site above other sites in the latter type of cell line.

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