Rønn Lars C B, Dissing Steen, Holm Arne, Berezin Vladimir, Bock Elisabeth
Protein Laboratory, Institute of Molecular Pathology, School of Medicine, University of Copenhagen, Panum Institute 6.2., Blegdamsvej 3, DK-2200 Copenhagen N, Denmark.
FEBS Lett. 2002 May 8;518(1-3):60-6. doi: 10.1016/s0014-5793(02)02644-3.
We have recently identified a synthetic peptide, termed C3, capable of binding the first immunoglobulin-like module of neural cell adhesion molecule (NCAM) by means of combinatorial chemistry and shown that this NCAM ligand promotes neurite outgrowth. By means of single cell calcium imaging using the calcium-sensitive probe fura-2-acetomethyl ester, we here show that the C3-peptide induced an increase in intracellular calcium in primary hippocampal neurons and PC12-E2 cells, presumably requiring mobilization of calcium from both extracellular and intracellular stores. We further observed that C3-induced neurite outgrowth was inhibited by antagonists of voltage-dependent calcium channels as well as by an inhibitor of intracellular calcium mobilization, TMB-8. These findings demonstrate at the single cell level that a synthetic NCAM ligand directly can induce an increase in intracellular calcium and suggest that NCAM-dependent neurite outgrowth requires calcium mobilization from both extracellular and intracellular calcium stores. Thus, the C3-peptide may be regarded as a useful tool for the study of NCAM-dependent signal transduction. Furthermore, the peptide may be of considerable therapeutical interest for the treatment of neurodegenerative disorders.
我们最近通过组合化学鉴定出一种名为C3的合成肽,它能够结合神经细胞粘附分子(NCAM)的首个免疫球蛋白样结构域,并表明这种NCAM配体可促进神经突生长。通过使用钙敏探针fura-2-乙酰甲酯进行单细胞钙成像,我们在此表明C3肽可诱导原代海马神经元和PC12-E2细胞内的细胞内钙增加,这可能需要从细胞外和细胞内储存库中动员钙。我们进一步观察到,电压依赖性钙通道拮抗剂以及细胞内钙动员抑制剂TMB-8可抑制C3诱导的神经突生长。这些发现表明,在单细胞水平上,合成的NCAM配体可直接诱导细胞内钙增加,并表明依赖NCAM的神经突生长需要从细胞外和细胞内钙储存库中动员钙。因此,C3肽可被视为研究依赖NCAM的信号转导的有用工具。此外,该肽对于神经退行性疾病的治疗可能具有相当大的治疗意义。