Lipid Biology Laboratory, RIKEN, Saitama, Japan.
Division of Molecular Interaction, Institute for Genetic Medicine, Hokkaido University Graduate School of Life Science, Sapporo, Japan.
FASEB J. 2020 May;34(5):6185-6197. doi: 10.1096/fj.201900065RR. Epub 2020 Mar 12.
During adhesion, cells develop filopodia to facilitate the attachment to the extracellular matrix. The small guanosine triphosphate (GTP)-binding protein, Cdc42, plays a central role in the formation of filopodia. It has been reported that Cdc42 activity is regulated by cholesterol (Chol). We examined Chol distribution in filopodia using Chol-binding domain 4 (D4) fragment of bacterial toxin, perfringolysin O that senses high membrane concentration of Chol. Our results indicate that fluorescent D4 was enriched at the tip of the outer leaflet of filopodia in the initiation phase of cell adhesion. This enrichment was accompanied by a defect of D4 labeling in the inner leaflet. Steady phase adhered cell experiment indicated that both Cdc42 and ATP-binding cassette transporter, ABCA1, were involved in the binding of D4 to the cell surface. Depletion of Chol activated Cdc42. Our results suggest that asymmetric distribution of Chol at the tip of filopodia induces activation of Cdc42, and thus, facilitates filopodia formation.
在黏附过程中,细胞会伸出丝状伪足以促进与细胞外基质的附着。小分子鸟苷三磷酸(GTP)结合蛋白 Cdc42 在丝状伪足的形成中起核心作用。据报道,Cdc42 的活性受到胆固醇(Chol)的调节。我们使用能感知细胞膜高胆固醇浓度的细菌毒素——产气荚膜梭菌溶细胞素 O 的 Chol 结合域 4(D4)片段,研究了丝状伪足中的 Chol 分布。结果表明,在细胞黏附起始阶段,荧光 D4 在外层质膜的丝状伪足尖端富集。这种富集伴随着内层质膜 D4 标记的缺陷。在稳定黏附的细胞实验中,我们发现 Cdc42 和三磷酸腺苷结合盒转运体 ABCA1 都参与了 D4 与细胞表面的结合。Chol 的耗竭激活了 Cdc42。我们的结果表明,Chol 在丝状伪足尖端的不对称分布诱导了 Cdc42 的激活,从而促进了丝状伪足的形成。