Department of Food Science and Nutrition, Pukyong National University 599-1, Nam-gu, Busan 608-737, Republic of Korea.
Int J Mol Med. 2012 May;29(5):741-6. doi: 10.3892/ijmm.2012.899. Epub 2012 Feb 1.
Chlorella vulgaris, a unicellular microalgae, exerts various biological effects; however their effect on proliferation signaling pathways in normal cells has not been studied. We investigated the effect of hot water extracts of Chlorella vulgaris (CVE) on cell proliferation and related signaling pathways in rat intestinal epithelial cells (IEC-6). CVE increased the expression of insulin-like growth factor-I receptor (IGF-IR) and the phosphorylation of focal adhesion kinase (FAK) and Src. In addition, CVE induced activation of the mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3-kinase (PI3K)/Akt pathways. We verified the increased phosphorylation of extracellular-signal-related kinase (ERK) and Akt and the increased expression of the PI3K regulatory subunit p85. CVE also influenced the canonical Wnt pathway through increased expression of the nuclear β-catenin, cyclin D1. Tyr-397 of FAK mediates interactions with Src homology 2 (SH2) domains in a number of other signaling proteins, including PI3K, PLC-γ, Shc, Grb7, Src and Nck2. Because CVE induced FAK activation, FAK may affect the Wnt pathway. Addition of a FAK inhibitor decreased the expression of nuclear β-catenin, cyclin D1 and c-myc, and increased the expression of cytosolic β-catenin. We conclude that CVE stimulated proliferation of IEC-6 cells via the MAPK, PI3K/Akt and canonical Wnt pathways, and that this affected the canonical Wnt pathway.
小球藻,一种单细胞微藻,具有多种生物效应;然而,其对正常细胞增殖信号通路的影响尚未得到研究。我们研究了小球藻热水提取物(CVE)对大鼠肠上皮细胞(IEC-6)细胞增殖及相关信号通路的影响。CVE 增加了胰岛素样生长因子-I 受体(IGF-IR)的表达和粘着斑激酶(FAK)和Src 的磷酸化。此外,CVE 诱导丝裂原激活蛋白激酶(MAPK)和磷脂酰肌醇 3-激酶(PI3K)/Akt 通路的激活。我们验证了细胞外信号调节激酶(ERK)和 Akt 的磷酸化增加以及 PI3K 调节亚基 p85 的表达增加。CVE 还通过增加核 β-连环蛋白和细胞周期蛋白 D1 的表达影响经典 Wnt 通路。FAK 的 Tyr-397 与包括 PI3K、PLC-γ、Shc、Grb7、Src 和 Nck2 在内的许多其他信号蛋白的Src 同源 2(SH2)结构域相互作用。由于 CVE 诱导 FAK 激活,FAK 可能影响 Wnt 通路。加入 FAK 抑制剂可降低核 β-连环蛋白、细胞周期蛋白 D1 和 c-myc 的表达,增加胞浆 β-连环蛋白的表达。我们得出结论,CVE 通过 MAPK、PI3K/Akt 和经典 Wnt 通路刺激 IEC-6 细胞增殖,从而影响经典 Wnt 通路。