ERα promotes murine hematopoietic regeneration through the Ire 1α-mediated unfolded protein response

被引:43
作者
Chapple, Richard H. [1 ]
Hu, Tianyuan [1 ]
Tseng, Yu-Jung [2 ]
Liu, Lu [3 ]
Kitano, Ayumi [1 ]
Luu, Victor [1 ]
Hoegenauer, Kevin A. [1 ]
Iwawaki, Takao [4 ]
Li, Qing [3 ]
Nakada, Daisuke [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Grad Program Translat Biol & Mol Med, Houston, TX 77030 USA
[3] Univ Michigan, Dept Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
[4] Kanazawa Med Univ, Med Res Inst, Dept Life Sci, Div Cell Med, Ishikari, Hokkaido, Japan
基金
美国国家卫生研究院;
关键词
ESTROGEN-RECEPTOR-ALPHA; STEM-CELL DIVISION; PROGENITOR CELLS; TRANSCRIPTION FACTOR; OXIDATIVE STRESS; CYCLE; GAMMA; MICE; RNA; REJUVENATION;
D O I
10.7554/eLife.31159
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Activation of the unfolded protein response (UPR) sustains protein homeostasis (proteostasis) and plays a fundamental role in tissue maintenance and longevity of organisms. Long-range control of UPR activation has been demonstrated in invertebrates, but such mechanisms in mammals remain elusive. Here, we show that the female sex hormone estrogen regulates the UPR in hematopoietic stem cells (HSCs). Estrogen treatment increases the capacity of HSCs to regenerate the hematopoietic system upon transplantation and accelerates regeneration after irradiation. We found that estrogen signals through estrogen receptor a (ER alpha) expressed in hematopoietic cells to activate the protective Ire1 alpha-Xbp1 branch of the UPR. Further, ER alpha mediated activation of the Ire1 alpha-Xbp1 pathway confers HSCs with resistance against proteotoxic stress and promotes regeneration. Our findings reveal a systemic mechanism through which HSC function is augmented for hematopoietic regeneration.
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收藏
页数:25
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