Codina Marta, García de la serrana Daniel, Sánchez-Gurmaches Joan, Montserrat Núria, Chistyakova Oxana, Navarro Isabel, Gutiérrez Joaquim
Departament de Fisiologia, Facultat de Biologia, Universitat de Barcelona, España. Av. Diagonal 645, E-08028 Barcelona, Spain.
Gen Comp Endocrinol. 2008 Jun;157(2):116-24. doi: 10.1016/j.ygcen.2008.04.009. Epub 2008 Apr 23.
Primary cultures of rainbow trout skeletal muscle cells were used to examine the role of insulin-like growth factor II (IGF-II) in fish muscle metabolism and growth, and to compare its main signal transduction pathways with those of IGF-I. IGF-II stimulated 2-deoxy-d-glucose (2-DG) uptake in trout myocytes at concentrations of between 5 and 100 nM, with similar maximal effects and temporal pattern to IGF-I (100 nM). The results of incubation with inhibitors (Wortmannin and CKB) indicated that IGF-II stimulates glucose uptake through the same mechanisms as IGF-I. In addition, IGF-II stimulated myoblast DNA synthesis (measured by thymidine incorporation) at relatively low concentrations (0.1-10 nM), with the maximum increase at 1 nM (167+/-17% with respect to control values). The cells were immunoreactive against ERK 1/2 MAPK and Akt/PKB, components of the two main signal transduction pathways for the IGF-I receptor. IGF-II stimulated the phosphorylation of the protein MAPK, especially at the proliferation stage (increases of up to 125.7+/-16.9% and 125.3+/-3.3% with respect to control in IGF-II- and IGF-I-treated cells, respectively). In contrast, the effects of both IGFs on the activation of the PI3K/Akt pathway were stronger in fully differentiated myocytes and in early-formed fibres (up to 359+/-18.5% in IGF-II-treated cells with respect to control). These results indicate that IGF-II has both mitogenic and metabolic effects in trout muscle cells, which are equivalent to those found in response to IGF-I. Both IGFs exert these effects though the same signalling pathways (MAPK and PI3K/Akt).
虹鳟鱼骨骼肌细胞的原代培养物用于研究胰岛素样生长因子II(IGF-II)在鱼类肌肉代谢和生长中的作用,并将其主要信号转导途径与IGF-I的进行比较。IGF-II在5至100 nM的浓度下刺激虹鳟鱼肌细胞摄取2-脱氧-D-葡萄糖(2-DG),其最大效应和时间模式与IGF-I(100 nM)相似。与抑制剂(渥曼青霉素和CKB)孵育的结果表明,IGF-II通过与IGF-I相同的机制刺激葡萄糖摄取。此外,IGF-II在相对较低的浓度(0.1-10 nM)下刺激成肌细胞DNA合成(通过胸苷掺入测量),在1 nM时增加最大(相对于对照值增加167±17%)。这些细胞对ERK 1/2 MAPK和Akt/PKB具有免疫反应性,它们是IGF-I受体的两个主要信号转导途径的组成部分。IGF-II刺激蛋白MAPK的磷酸化,尤其是在增殖阶段(IGF-II处理的细胞和IGF-I处理的细胞相对于对照分别增加高达125.7±16.9%和125.3±3.3%)。相反,两种IGF对PI3K/Akt途径激活的作用在完全分化的肌细胞和早期形成的纤维中更强(IGF-II处理的细胞相对于对照高达359±18.5%)。这些结果表明,IGF-II在虹鳟鱼肌肉细胞中具有促有丝分裂和代谢作用,这与对IGF-I的反应中发现的作用相当。两种IGF都通过相同的信号通路(MAPK和PI3K/Akt)发挥这些作用。