Myosin Vb interacts with Rab8a on a tubular network containing EHD1 and EHD3

被引:130
作者
Roland, Joseph T.
Kenworthy, Anne K.
Peranen, Johan
Caplan, Steve
Goldenring, James R.
机构
[1] Vanderbilt Univ, Sch Med, Dept Surg, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[4] Vet Affairs Med Ctr, Nashville, TN 37212 USA
[5] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[6] Univ Nebraska, Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
关键词
D O I
10.1091/mbc.E07-02-0169
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Cells use multiple pathways to internalize and recycle cell surface components. Although Rablla and Myosin Vb are involved in the recycling of proteins internalized by clathrin-mediated endocytosis, Rab8a has been implicated in nonclathrin-dependent endocytosis and recycling. By yeast two-hybrid assays, we have now demonstrated that Myosin Vb can interact with Rab8a, but not Rab8b. We have confirmed the interaction of Myosin Vb with Rab11a and Rab8a in vivo by using fluorescent resonant energy transfer techniques. Rab8a and Myosin Vb colocalize to a tubular network containing EHD1 and EHD3, which does not contain Rab11a. Myosin Vb tail can cause the accumulation of both Rab11a and Rab8a in collapsed membrane cisternae, whereas dominant-negative Rab11FIP2(129-512) selectively accumulates Rablla but not Rab8a. Additionally, dynamic live cell imaging demonstrates distinct pathways for Rablla and Rab8a vesicle trafficking. These findings indicate that Rab8a and Rab11a define different recycling pathways that both use Myosin Vb.
引用
收藏
页码:2828 / 2837
页数:10
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