Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
Cytoskeleton (Hoboken). 2012 Oct;69(10):810-8. doi: 10.1002/cm.21055. Epub 2012 Aug 28.
Cytokinesis, the last step during cell division, is a highly coordinated process that involves the relay of signals from both the outside and inside of the cell. We have a basic understanding of how cells regulate internal events, but how cells respond to extracellular cues is less explored. In a systematic RNAi screen of G protein-coupled receptors (GPCRs) and their effectors, we found that some GPCRs are involved in cytokinesis. RNAi knockdown of these GPCRs caused increased binucleated cell formation, and live cell imaging showed that most formed midbodies but failed at the abscission stage. OR2A4 (olfactory receptor, family 2, subfamily A, member 4) localized to cytokinetic structures in cells and its knockdown caused cytokinesis failure at an earlier stage, likely due to effects on the actin cytoskeleton. Identifying the downstream components that transmit GPCR signals during cytokinesis will be the next step and we show that GIPC1 (GIPC PDZ domain containing family, member 1), an adaptor protein for GPCRs, may play a part. RNAi knockdown of GIPC1 significantly increased binucleated cell formation. Understanding the molecular details of GPCRs and their interaction proteins in cytokinesis regulation will give us important clues about GPCRs signaling as well as how cells communicate with their environment during division.
胞质分裂是细胞分裂的最后一步,是一个高度协调的过程,涉及细胞内外信号的传递。我们对细胞如何调节内部事件有了基本的了解,但细胞如何对外界线索做出反应还不太清楚。在一项针对 G 蛋白偶联受体 (GPCR) 及其效应物的系统 RNAi 筛选中,我们发现一些 GPCR 参与了胞质分裂。这些 GPCR 的 RNAi 敲低导致双核细胞形成增加,活细胞成像显示大多数形成了中体,但在分离阶段失败。OR2A4(嗅觉受体,家族 2,亚家族 A,成员 4)定位于细胞中的胞质分裂结构,其敲低导致胞质分裂在早期失败,可能是由于对肌动蛋白细胞骨架的影响。确定胞质分裂过程中 GPCR 信号传递的下游成分将是下一步,我们表明 GIPC1(GIPC PDZ 结构域包含家族,成员 1),一种 GPCR 的衔接蛋白,可能起作用。GIPC1 的 RNAi 敲低显著增加了双核细胞的形成。了解 GPCR 及其在胞质分裂调节中的相互作用蛋白的分子细节将为我们提供关于 GPCR 信号以及细胞在分裂过程中如何与环境进行通信的重要线索。