Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
J Invest Dermatol. 2020 Sep;140(9):1743-1752.e4. doi: 10.1016/j.jid.2020.01.015. Epub 2020 Feb 3.
IGF-1 receptor (IGF1R) signaling promotes keratinocyte proliferation, migration, and survival. However, the mechanism of IGF1R endocytosis in normal keratinocytes remains unclear. Confocal, super resolution structured illumination microscopy, total internal reflection fluorescence microscopy, and coimmunoprecipitation studies reveal that IGF1R associates with flotillin-1 (Flot-1), which currently has no known role in normal receptor tyrosine kinase endocytosis, under basal conditions in monolayer keratinocyte cultures. Ligand stimulation of IGF1R promotes its clathrin-dependent endocytosis, mediated by two distinct adaptors, Flot-1 in noncaveolar lipid rafts and the AP2A1/2 complex in clathrin vesicles. Concurrent, but not individual, short hairpin RNA knockdown of FLOT1/2 and AP2A1/2 reduced IGF1R association with clathrin, internalization, and pathway activation by more than 50% (of phosphorylated IGF1R, phosphorylated protein kinase B, and phosphorylated MAPK kinase), suggesting the complementarity of these two adaptor-specific pathways. The Flot-1 pathway is more responsive to low IGF-1 concentrations, whereas the AP2A1/2 pathway predominates at higher IGF-1 concentrations. Selective association of IGF1R-Flot-1-clathrin with Rab4, but IGF1R-AP2A1/2-clathrin with Rab11, implicates Flot-1 as the adaptor for faster recycling and AP2A1/2 as the adaptor for slower IGF1R recycling. These dual pathways, particularly flotillin-dependent, clathrin-mediated endocytosis, provide a new avenue for drug targeting in disorders with aberrant regulation of IGF1R signaling.
IGF-1 受体(IGF1R)信号促进角质形成细胞的增殖、迁移和存活。然而,正常角质形成细胞中 IGF1R 内吞的机制仍不清楚。共聚焦、超分辨率结构光照明显微镜、全内反射荧光显微镜和共免疫沉淀研究表明,在单层角质形成细胞培养物的基础条件下,IGF1R 与目前在正常受体酪氨酸激酶内吞中没有已知作用的 flotillin-1(Flot-1)相关。IGF1R 的配体刺激促进其网格蛋白依赖性内吞作用,由两个不同的衔接子介导,即非小窝脂筏中的 Flot-1 和网格蛋白小泡中的 AP2A1/2 复合物。同时,而不是单独的短发夹 RNA 敲低 FLOT1/2 和 AP2A1/2,减少了 IGF1R 与网格蛋白、内化和途径激活的关联超过 50%(磷酸化 IGF1R、磷酸化蛋白激酶 B 和磷酸化 MAPK 激酶),表明这两种衔接子特异性途径的互补性。Flot-1 途径对低 IGF-1 浓度更敏感,而 AP2A1/2 途径在较高 IGF-1 浓度时占主导地位。IGF1R-Flot-1-网格蛋白与 Rab4 的选择性结合,而 IGF1R-AP2A1/2-网格蛋白与 Rab11 的结合,表明 Flot-1 是更快回收的衔接子,而 AP2A1/2 是较慢 IGF1R 回收的衔接子。这些双途径,特别是 flotillin 依赖性、网格蛋白介导的内吞作用,为具有异常 IGF1R 信号调节的疾病提供了药物靶向的新途径。