IRE1α activation protects mice against acetaminophen-induced hepatotoxicity

Journal of Experimental Medicine - Tập 209 Số 2 - Trang 307-318 - 2012
Kyu Yeon Hur1, Jae‐Seon So1, Vera M. Ruda2, Maria Frank-Kamenetsky3, Kevin Fitzgerald3, Victor Koteliansky3, Takao Iwawaki4,5,6, Laurie H. Glimcher1,7,8, Ann–Hwee Lee1,7
1Deartment of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115 1
2Cardiovascular Research Center and Center for Human Genetic Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 2
3Alnylam Pharmaceuticals, Cambridge, MA 02142 3
4Advanced Scientific Research Leaders Development Unit, Gunma University, Gunma 371-8511, Japan 6
5Iwawaki Initiative Research Unit, Institute of Physical and Chemical Research, Wako, Saitama 351-0198, Japan 4
6PRESTO, Japan Science and Technology Agency, Kawaguchi, Saitama 332--0012, Japan 5
7Dept of Medicine, Harvard Medical School, Boston, MA 02115 7
8Ragon Institute of MGH, MIT, and Harvard, Boston, MA 02115 8

Tóm tắt

The mammalian stress sensor IRE1α plays a central role in the unfolded protein, or endoplasmic reticulum (ER), stress response by activating its downstream transcription factor XBP1 via an unconventional splicing mechanism. IRE1α can also induce the degradation of a subset of mRNAs in a process termed regulated IRE1-dependent decay (RIDD). Although diverse mRNA species can be degraded by IRE1α in vitro, the pathophysiological functions of RIDD are only beginning to be explored. Acetaminophen (APAP) overdose is the most frequent cause of acute liver failure in young adults in the United States and is primarily caused by CYP1A2-, CYP2E1-, and CYP3A4-driven conversion of APAP into hepatotoxic metabolites. We demonstrate here that genetic ablation of XBP1 results in constitutive IRE1α activation in the liver, leading to RIDD of Cyp1a2 and Cyp2e1 mRNAs, reduced JNK activation, and protection of mice from APAP-induced hepatotoxicity. A pharmacological ER stress inducer that activated IRE1α suppressed the expression of Cyp1a2 and Cyp2e1 in WT, but not IRE1α-deficient mouse liver, indicating the essential role of IRE1α in the down-regulation of these mRNAs upon ER stress. Our study reveals an unexpected function of RIDD in drug metabolism.

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