Blaser Heiko, Reichman-Fried Michal, Castanon Irinka, Dumstrei Karin, Marlow Florence L, Kawakami Koichi, Solnica-Krezel Lilianna, Heisenberg Carl-Philipp, Raz Erez
Germ Cell Development, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
Dev Cell. 2006 Nov;11(5):613-27. doi: 10.1016/j.devcel.2006.09.023.
The molecular and cellular mechanisms governing cell motility and directed migration in response to the chemokine SDF-1 are largely unknown. Here, we demonstrate that zebrafish primordial germ cells whose migration is guided by SDF-1 generate bleb-like protrusions that are powered by cytoplasmic flow. Protrusions are formed at sites of higher levels of free calcium where activation of myosin contraction occurs. Separation of the acto-myosin cortex from the plasma membrane at these sites is followed by a flow of cytoplasm into the forming bleb. We propose that polarized activation of the receptor CXCR4 leads to a rise in free calcium that in turn activates myosin contraction in the part of the cell responding to higher levels of the ligand SDF-1. The biased formation of new protrusions in a particular region of the cell in response to SDF-1 defines the leading edge and the direction of cell migration.
趋化因子SDF-1引导细胞运动和定向迁移的分子和细胞机制在很大程度上尚不清楚。在此,我们证明,迁移受SDF-1引导的斑马鱼原始生殖细胞会产生由细胞质流动驱动的泡状突起。突起在游离钙水平较高且发生肌球蛋白收缩激活的部位形成。在这些部位,肌动球蛋白皮层与质膜分离,随后细胞质流入形成的泡中。我们提出,受体CXCR4的极化激活导致游离钙升高,进而激活细胞中对较高水平配体SDF-1作出反应的部分区域的肌球蛋白收缩。细胞特定区域响应SDF-1而有偏向地形成新的突起,这确定了细胞迁移的前缘和方向。