Hölttä-Vuori Maarit, Alpy Fabien, Tanhuanpää Kimmo, Jokitalo Eija, Mutka Aino-Liisa, Ikonen Elina
Institute of Biomedicine, University of Helsinki, 00014 Helsinki, Finland.
Mol Biol Cell. 2005 Aug;16(8):3873-86. doi: 10.1091/mbc.e04-12-1105. Epub 2005 Jun 1.
MLN64 is a late endosomal cholesterol-binding membrane protein of an unknown function. Here, we show that MLN64 depletion results in the dispersion of late endocytic organelles to the cell periphery similarly as upon pharmacological actin disruption. The dispersed organelles in MLN64 knockdown cells exhibited decreased association with actin and the Arp2/3 complex subunit p34-Arc. MLN64 depletion was accompanied by impaired fusion of late endocytic organelles and delayed cargo degradation. MLN64 overexpression increased the number of actin and p34-Arc-positive patches on late endosomes, enhanced the fusion of late endocytic organelles in an actin-dependent manner, and stimulated the deposition of sterol in late endosomes harboring the protein. Overexpression of wild-type MLN64 was capable of rescuing the endosome dispersion in MLN64-depleted cells, whereas mutants of MLN64 defective in cholesterol binding were not, suggesting a functional connection between MLN64-mediated sterol transfer and actin-dependent late endosome dynamics. We propose that local sterol enrichment by MLN64 in the late endosomal membranes facilitates their association with actin, thereby governing actin-dependent fusion and degradative activity of late endocytic organelles.
MLN64是一种功能未知的晚期内体胆固醇结合膜蛋白。在此,我们表明,MLN64缺失导致晚期内吞细胞器分散至细胞周边,这与药物性肌动蛋白破坏后的情况类似。MLN64基因敲低细胞中分散的细胞器与肌动蛋白和Arp2/3复合体亚基p34-Arc的结合减少。MLN64缺失伴随着晚期内吞细胞器融合受损和货物降解延迟。MLN64过表达增加了晚期内体上肌动蛋白和p34-Arc阳性斑块的数量,以肌动蛋白依赖的方式增强了晚期内吞细胞器的融合,并刺激了含有该蛋白的晚期内体中固醇的沉积。野生型MLN64的过表达能够挽救MLN64缺失细胞中的内体分散,而胆固醇结合缺陷的MLN64突变体则不能,这表明MLN64介导的固醇转移与肌动蛋白依赖的晚期内体动力学之间存在功能联系。我们提出,MLN64在晚期内体膜中局部富集固醇有助于它们与肌动蛋白结合,从而控制晚期内吞细胞器的肌动蛋白依赖融合和降解活性。