Russo Lilian C, Goñi Camila N, Castro Leandro M, Asega Amanda F, Camargo Antonio C M, Trujillo Cleber A, Ulrich Henning, Glucksman Marc J, Scavone Cristoforo, Ferro Emer S
Department of Cell Biology and Development, Institute of Biomedical Sciences, University of São Paulo, Brazil.
FEBS J. 2009 Aug;276(16):4358-71. doi: 10.1111/j.1742-4658.2009.07144.x. Epub 2009 Jul 15.
Thimet oligopeptidase (EC 3.4.24.15; EP24.15) was originally described as a neuropeptide-metabolizing enzyme, highly expressed in the brain, kidneys and neuroendocrine tissue. EP24.15 lacks a typical signal peptide sequence for entry into the secretory pathway and is secreted by cells via an unconventional and unknown mechanism. In this study, we identified a novel calcium-dependent interaction between EP24.15 and calmodulin, which is important for the stimulated, but not constitutive, secretion of EP24.15. We demonstrated that, in vitro, EP24.15 and calmodulin physically interact only in the presence of Ca2+, with an estimated Kd value of 0.52 mum. Confocal microscopy confirmed that EP24.15 colocalizes with calmodulin in the cytosol of resting HEK293 cells. This colocalization markedly increases when cells are treated with either the calcium ionophore A23187 or the protein kinase A activator forskolin. Overexpression of calmodulin in HEK293 cells is sufficient to greatly increase the A23187-stimulated secretion of EP24.15, which can be inhibited by the calmodulin inhibitor calmidazolium. The specific inhibition of protein kinase A with KT5720 reduces the A23187-stimulated secretion of EP24.15 and inhibits the synergistic effects of forskolin with A23187. Treatment with calmidazolium and KT5720 nearly abolishes the stimulatory effects of A23187 on EP24.15 secretion. Together, these data suggest that the interaction between EP24.15 and calmodulin is regulated within cells and is important for the stimulated secretion of EP24.15 from HEK293 cells.
硫醇寡肽酶(EC 3.4.24.15;EP24.15)最初被描述为一种神经肽代谢酶,在脑、肾和神经内分泌组织中高度表达。EP24.15缺乏进入分泌途径的典型信号肽序列,细胞通过一种非常规且未知的机制分泌该酶。在本研究中,我们鉴定出EP24.15与钙调蛋白之间存在一种新的钙依赖性相互作用,这对EP24.15的刺激型而非组成型分泌很重要。我们证明,在体外,EP24.15和钙调蛋白仅在Ca2+存在时发生物理相互作用,估计解离常数(Kd)值为0.52 μM。共聚焦显微镜检查证实,在静止的HEK293细胞胞质溶胶中,EP24.15与钙调蛋白共定位。当用钙离子载体A23187或蛋白激酶A激活剂福斯可林处理细胞时,这种共定位显著增加。在HEK293细胞中过表达钙调蛋白足以大幅增加A23187刺激的EP24.15分泌,而钙调蛋白抑制剂氯米达唑可抑制这种分泌。用KT5720特异性抑制蛋白激酶A可降低A23187刺激的EP24.15分泌,并抑制福斯可林与A23187的协同作用。用氯米达唑和KT5720处理几乎消除了A23187对EP24.15分泌的刺激作用。总之,这些数据表明,EP24.15与钙调蛋白之间的相互作用在细胞内受到调节,并且对HEK293细胞中EP24.15的刺激型分泌很重要。