The human thioredoxin reductase-1 splice variant TXNRD1_v3 is an atypical inducer of cytoplasmic filaments and cell membrane filopodia

被引:21
作者
Damdimopoulou, Pauliina E. [1 ,2 ]
Miranda-Vizuete, Antonio [3 ]
Arner, Elias S. J. [4 ]
Gustafsson, Jan-Ake [1 ]
Damdimopoulos, Anastasios E. [1 ]
机构
[1] Novum, Karolinska Inst, Dept Biosci & Nutr, SE-14157 Huddinge, Sweden
[2] Univ Turku, FI-20520 Turku, Finland
[3] Univ Pablo Olavide, Dept Anat Fisiol & Biol Celular, CABD, CSIC, Seville 41013, Spain
[4] Karolinska Inst, Div Biochem, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2009年 / 1793卷 / 10期
基金
瑞典研究理事会;
关键词
Thioredoxin reductase; Cytoskeleton; Actin; Filopodia; REDOX REGULATION; STRUCTURAL BASIS; ACTIN; PROTEIN; THIOREDOXIN-REDUCTASE-1; ACTIVATION; COMPLEX; DOMAIN; FOCUS; WASP;
D O I
10.1016/j.bbamcr.2009.07.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thioredoxin reductases are important selenoproteins maintaining cellular redox balance and regulating several redox dependent processes in apoptosis, cell proliferation and differentiation. Specific functions of dedicated splice variants may add further complexity to the functions of these proteins. We show here that a splice variant of human thioredoxin reductase 1, TXNRD1_v3, forms both dynamic cytoplasmic filaments and provokes instantaneous formation of dynamic cell membrane protrusions identified as filopodia. Using truncated versions of the protein we found that both the cytoplasmic filaments and the filopodia formation were exclusively dependent on the glutaredoxin domain of the protein. Interestingly, actin polymerization was required for filopodia formation triggered by T-XNRD1_v3, but not for generation of cytoplasmic filaments. We conclude that the glutaredoxin domain of TXNRD1_v3 is an atypical regulator of the cell cytoskeleton that potently induces formation of highly ordered cytoplasmic filaments and cell membrane filopodia. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1588 / 1596
页数:9
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