Academic Journal

Asparagine protects pericentral hepatocytes during acute liver injury

التفاصيل البيبلوغرافية
العنوان: Asparagine protects pericentral hepatocytes during acute liver injury
المؤلفون: Yu Sun, Hadrien Demagny, Adrien Faure, Francesca Pontanari, Antoine Jalil, Nadia Bresciani, Ece Yildiz, Melanie Korbelius, Alessia Perino, Kristina Schoonjans
المصدر: The Journal of Clinical Investigation, Vol 133, Iss 7 (2023)
بيانات النشر: American Society for Clinical Investigation, 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine
مصطلحات موضوعية: Hepatology, Metabolism, Medicine
الوصف: The nonessential amino acid asparagine can only be synthesized de novo by the enzymatic activity of asparagine synthetase (ASNS). While ASNS and asparagine have been implicated in the response to numerous metabolic stressors in cultured cells, the in vivo relevance of this enzyme in stress-related pathways remains unexplored. Here, we found ASNS to be expressed in pericentral hepatocytes, a population of hepatic cells specialized in xenobiotic detoxification. ASNS expression was strongly enhanced in 2 models of acute liver injury: carbon tetrachloride (CCl4) and acetaminophen. We found that mice with hepatocyte-specific Asns deletion were more prone to pericentral liver damage than their control littermates after toxin exposure. This phenotype could be reverted by i.v. administration of asparagine. Unexpectedly, the stress-induced upregulation of ASNS involved an ATF4-independent, noncanonical pathway mediated by the nuclear receptor, liver receptor homolog 1 (LRH-1; NR5A2). Altogether, our data indicate that the induction of the asparagine-producing enzyme ASNS acts as an adaptive mechanism to constrain the necrotic wave that follows toxin administration and provide proof of concept that i.v. delivery of asparagine can dampen hepatotoxin-induced pericentral hepatocellular death.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1558-8238
Relation: https://doaj.org/toc/1558-8238
DOI: 10.1172/JCI163508
URL الوصول: https://doaj.org/article/eb763ef9953c42d3ac3eebba53634aa7
رقم الانضمام: edsdoj.b763ef9953c42d3ac3eebba53634aa7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:15588238
DOI:10.1172/JCI163508