Dkk3/REIC, an N-glycosylated Protein, Is a Physiological Endoplasmic Reticulum Stress Inducer in the Mouse Adrenal Gland

被引:2
作者
Fujita, Hirofumi [1 ]
Bando, Tetsuya [1 ]
Oyadomari, Seiichi [4 ]
Ochiai, Kazuhiko [5 ]
Watanabe, Masami [2 ]
Kumon, Hiromi [3 ,6 ]
Ohuchi, Hideyo [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Cytol & Histol, Okayama, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Urol, Okayama, Japan
[3] Okayama Univ, Innovat Ctr Okayama Nanobio Targeted Therapy, Okayama 7008558, Japan
[4] Univ Tokushima, Inst Genome Res, Div Mol Biol, Tokushima 7708503, Japan
[5] Nippon Vet & Life Sci Univ, Fac Vet Sci, Sch Vet Nursing & Technol, Dept Basic Sci, Musashino, Tokyo 1808602, Japan
[6] Niimi Univ, Okayama 7188585, Japan
关键词
Dkk3 knockout mouse; adrenal gland; glucose-regulated protein 78; proteome; endoplasmic reticulum stress; GENE; ACTIVATION; EXPRESSION; APOPTOSIS; FAMILY; CANCER; ROLES; CELLS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dickkopf 3 (Dkk3) is a secreted protein belonging to the Dkk family and encoded by the orthologous gene of REIC. Dkk3/REIC is expressed by mouse and human adrenal glands, but the understanding of its roles in this organ is still limited. To determine the functions of Dkk3 in the mouse adrenal gland, we first identified that the mouse Dkk3 protein is N-glycosylated in the adrenal gland as well as in the brain. We performed proteome analysis on adrenal glands from Dkk3-null mice, in which exons 5 and 6 of the Dkk3 gene are deleted. Two-dimensional polyacrylamide gel electrophoresis of adrenal proteins from wild-type and Dkk3-null mice revealed 5 protein spots whose intensities were altered between the 2 genotypes. Mass spectrometry analysis of these spots identified binding immunoglobulin protein (BiP), an endoplasmic reticulum (ER) chaperone. To determine whether mouse Dkk3 is involved in the unfolded protein response (UPR), we carried out a reporter assay using ER-stress responsive elements. Forced expression of Dkk3 resulted in the induction of distinct levels of reporter expression, showing the UPR initiated by the ER membrane proteins of activating transcription factor 6 (ATF6) and inositol-requring enzyme 1 (IRE1). Thus, it is possible that Dkk3 is a physiological ER stressor in the mouse adrenal gland.
引用
收藏
页码:199 / 208
页数:10
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