Department of Obstetrics and Gynecology, Ludwig Maximilians University of Munich, Maistrasse 11, 80337 Munich, Germany.
Mol Hum Reprod. 2011 Dec;17(12):747-57. doi: 10.1093/molehr/gar053. Epub 2011 Aug 10.
Galectin-1 (gal-1), a member of the mammalian β-galactoside-binding proteins, exerts biological effects by recognition of glycan ligands, including those involved in cell adhesion and growth regulation. In a previous study, we demonstrated that gal-1 induces cell differentiation processes on the membrane of choriocarcinoma cells BeWo, including the receptor tyrosine kinases, REarranged during transfection, janus kinase 2 and vascular endothelial growth factor receptor 3. Within this study, we examined which mitogen-activated protein kinases (MAPK) and serine/threonine kinases were phoshorylated by gal-1. Out of a number of 21 different MAPKs and other serine/threonine kinases, the stimulation of BeWo cells with gal-1 showed a significant alteration of signal intensity in extracellular-regulated kinases 1/2 (ERK1/2), Akt-3, Akt-pan and glycogen synthase kinase-α/β (GSK-3α/β). We demonstrated that gal-1 significantly inhibited ERK1/2, Akt-3/pan and GSK-3α/β phosphorylation in BeWo cells and in addition induced Elk1 transcription factor activation. In contrast to gal-1 effects, MAPK inhibitor U0126 reduced syncytium formation of BeWo cells. The results of our data showed that phosphorylation of MAP kinases are involved in gal-1-induced signal transduction processes in BeWo cells. Additional results obtained with MAPK inhibitor U0126 close the gap between syncytium formation induced by gal-1 and MAPK activation in trophoblast cells. Furthermore, we demonstrated that gal-1 induces the activation of Elk1, a transcription factor that is activated by MAPK pathways.
半乳糖凝集素-1(gal-1)是哺乳动物β-半乳糖苷结合蛋白家族的成员,通过识别糖配体发挥生物学作用,包括参与细胞黏附和生长调节的糖配体。在之前的研究中,我们证明 gal-1 诱导绒毛膜癌细胞 BeWo 膜上的细胞分化过程,包括受体酪氨酸激酶、转染时重排、Janus 激酶 2 和血管内皮生长因子受体 3。在本研究中,我们研究了 gal-1 磷酸化哪些丝裂原活化蛋白激酶(MAPK)和丝氨酸/苏氨酸激酶。在 21 种不同的 MAPK 和其他丝氨酸/苏氨酸激酶中,gal-1 刺激 BeWo 细胞显示细胞外调节激酶 1/2(ERK1/2)、Akt-3、Akt-全谱和糖原合酶激酶-α/β(GSK-3α/β)的信号强度显著改变。我们证明 gal-1 显著抑制 BeWo 细胞中 ERK1/2、Akt-3/全谱和 GSK-3α/β 的磷酸化,并且诱导 Elk1 转录因子激活。与 gal-1 作用相反,MAPK 抑制剂 U0126 减少 BeWo 细胞的合体形成。我们的数据结果表明,MAP 激酶的磷酸化参与 gal-1 诱导的 BeWo 细胞信号转导过程。用 MAPK 抑制剂 U0126 获得的其他结果弥合了 gal-1 诱导的合胞体形成与滋养细胞中 MAPK 激活之间的差距。此外,我们证明 gal-1 诱导 Elk1 的激活,Elk1 是一种被 MAPK 途径激活的转录因子。