Boric acid induces cytoplasmic stress granule formation, eIF2α phosphorylation, and ATF4 in prostate DU-145 cells

被引:36
作者
Henderson, Kimberly A. [1 ]
Kobylewski, Sarah E. [1 ]
Yamada, Kristin E. [1 ]
Eckhert, Curtis D. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Interdept Program Mol Toxicol, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Dept Environm Hlth Sci, Charles E Young Dr, Los Angeles, CA 90095 USA
关键词
Boron; Boric acid; eIF2; alpha; ATF4; DU-145; cells; UNFOLDED PROTEIN RESPONSE; INHIBITS HUMAN PROSTATE; NECROSIS-FACTOR-ALPHA; ENDOPLASMIC-RETICULUM; DIETARY BORON; CANCER; BORATE; IDENTIFICATION; REGULATOR; TOXICITY;
D O I
10.1007/s10534-014-9809-5
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
Dietary boron intake is associated with reduced prostate and lung cancer risk and increased bone mass. Boron is absorbed and circulated as boric acid (BA) and at physiological concentrations is a reversible competitive inhibitor of cyclic ADP ribose, the endogenous agonist of the ryanodine receptor calcium (Ca+2) channel, and lowers endoplasmic reticulum (ER) [Ca]. Low ER [Ca2+] has been reported to induce ER stress and activate the eIF2 alpha/ATF4 pathway. Here we report that treatment of DU145 prostate cells with physiological levels of BA induces ER stress with the formation of stress granules and mild activation of eIF2 alpha, GRP78/BiP, and ATF4. Mild activation of eIF2 alpha and its downstream transcription factor, ATF4, enables cells to reconfigure gene expression to manage stress conditions and mild activation of ATF4 is also required for the differentiation of osteoblast cells. Our results using physiological levels of boric acid identify the eIF2 alpha/ATF pathway as a plausible mode of action that underpins the reported health effects of dietary boron.
引用
收藏
页码:133 / 141
页数:9
相关论文
共 52 条
[1]  
Anderson P, 2002, J CELL SCI, V115, P3227
[2]  
Armstrong TA, 2003, J ANIM SCI, V81, P2552
[3]  
Barranco WT, 2007, CANCER CAUSE CONTROL, V18, P583, DOI 10.1007/s10552-007-9023-7
[4]   Evaluation of ecological and in vitro effects of boron on prostate cancer risk (United States) [J].
Barranco, Wade T. ;
Hudak, Paul F. ;
Eckhert, Curtis D. .
CANCER CAUSES & CONTROL, 2007, 18 (01) :71-77
[5]   Boric acid inhibits human prostate cancer cell proliferation [J].
Barranco, WT ;
Eckhert, CD .
CANCER LETTERS, 2004, 216 (01) :21-29
[6]   Cellular changes in boric acid-treated DU-145 prostate cancer cells [J].
Barranco, WT ;
Eckhert, CD .
BRITISH JOURNAL OF CANCER, 2006, 94 (06) :884-890
[7]   Three RNA Recognition Motifs Participate in RNA Recognition and Structural Organization by the Pro-Apoptotic Factor TIA-1 [J].
Bauer, William J. ;
Heath, Jason ;
Jenkins, Jermaine L. ;
Kielkopf, Clara L. .
JOURNAL OF MOLECULAR BIOLOGY, 2012, 415 (04) :727-740
[8]   Boron modulates extracellular matrix and TNFα synthesis in human fibroblasts [J].
Benderdour, M ;
Hess, K ;
Dzondo-Gadet, M ;
Nabet, P ;
Belleville, F ;
Dousset, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 246 (03) :746-751
[9]   Boron stimulates yeast (Saccharomyces cerevisiae) growth [J].
Bennett, A ;
Rowe, RI ;
Soch, N ;
Eckhert, CD .
JOURNAL OF NUTRITION, 1999, 129 (12) :2236-2238
[10]   The endoplasmic reticulum: a multifunctional signaling organelle [J].
Berridge, MJ .
CELL CALCIUM, 2002, 32 (5-6) :235-249