Saidi Mouna, Kamali Soufiane, Ruiz Alberto Orduna, Beaudry Francis
Groupe de Recherche en Pharmacologie Animal du Québec (GREPAQ), Département de Biomédecine Vétérinaire, Faculté de Médecine Vétérinaire, Université de Montréal, 3200 Sicotte, Saint-Hyacinthe, QC, J2S 2M2, Canada.
Neurochem Res. 2015 Nov;40(11):2304-16. doi: 10.1007/s11064-015-1720-0. Epub 2015 Sep 15.
Substance P (SP) play a central role in nociceptive transmission and it is an agonist of the Neurokinin-1 receptor located in the lamina I of the spinal cord. SP is a major proteolytic product of the protachykinin-1 primarily synthesized in neurons. Proprotein convertases (PCs) are extensively expressed in the central nervous system and specifically cleave at C-terminal of either a pair of basic amino acids, or a single basic residue. The proteolysis control of endogenous protachykinins has a profound impact on pain perception and the role of PCs remain unclear. The objective of this study was to decipher the role of PC1 and PC2 in the proteolysis surrogate protachykinins (i.e. Tachykinin 20-68 and Tachykinin 58-78) using cellular fractions of spinal cords from wild type (WT), PC1(-/+) and PC2(-/+) animals and mass spectrometry. Full-length Tachykinin 20-68 and Tachykinin 58-78 was incubated for 30 min in WT, PC1(-/+) and PC2(-/+) mouse spinal cord S9 fractions and specific C-terminal peptide fragments were identified and quantified by mass spectrometry. The results clearly demonstrate that both PC1 and PC2 mediate the formation of SP and Tachykinin 58-71, an important SP precursor, with over 50 % reduction of the rate of formation in mutant PC1 and PC2 mouse S9 spinal cord fractions. The results obtained revealed that PC1 and PC2 are involved in the C-terminal processing of protachykinin peptides and suggest a major role in the maturation of the protachykinin-1 protein.
P物质(SP)在伤害性感受传递中起核心作用,它是位于脊髓I层的神经激肽-1受体的激动剂。SP是主要在神经元中合成的前速激肽原-1的主要蛋白水解产物。前蛋白转化酶(PCs)在中枢神经系统中广泛表达,并特异性地在一对碱性氨基酸的C末端或单个碱性残基处切割。内源性前速激肽原的蛋白水解控制对疼痛感知有深远影响,而PCs的作用仍不清楚。本研究的目的是使用野生型(WT)、PC1(-/+)和PC2(-/+)动物脊髓的细胞组分和质谱法来解读PC1和PC2在蛋白水解替代前速激肽原(即速激肽20-68和速激肽58-78)中的作用。将全长速激肽20-68和速激肽58-78在WT、PC1(-/+)和PC2(-/+)小鼠脊髓S9组分中孵育30分钟,通过质谱法鉴定和定量特定的C末端肽片段。结果清楚地表明,PC1和PC2都介导了SP和重要的SP前体速激肽58-71的形成,在突变型PC1和PC2小鼠脊髓S9组分中形成速率降低了50%以上。所得结果表明,PC1和PC2参与前速激肽原肽的C末端加工,并提示其在前速激肽原-1蛋白成熟中起主要作用。