Academic Journal

Farnesoid X receptor activation by bile acids suppresses lipid peroxidation and ferroptosis

التفاصيل البيبلوغرافية
العنوان: Farnesoid X receptor activation by bile acids suppresses lipid peroxidation and ferroptosis
المؤلفون: Juliane Tschuck, Lea Theilacker, Ina Rothenaigner, Stefanie A. I. Weiß, Banu Akdogan, Van Thanh Lam, Constanze Müller, Roman Graf, Stefanie Brandner, Christian Pütz, Tamara Rieder, Philippe Schmitt-Kopplin, Michelle Vincendeau, Hans Zischka, Kenji Schorpp, Kamyar Hadian
المصدر: Nature Communications, Vol 14, Iss 1, Pp 1-13 (2023)
بيانات النشر: Nature Portfolio
سنة النشر: 2023
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Science
الوصف: Ferroptosis is a regulated cell death modality that occurs upon iron-dependent lipid peroxidation. Recent research has identified many regulators that induce or inhibit ferroptosis; yet, many regulatory processes and networks remain to be elucidated. In this study, we performed a chemical genetics screen using small molecules with known mode of action and identified two agonists of the nuclear receptor Farnesoid X Receptor (FXR) that suppress ferroptosis, but not apoptosis or necroptosis. We demonstrate that in liver cells with high FXR levels, knockout or inhibition of FXR sensitized cells to ferroptotic cell death, whereas activation of FXR by bile acids inhibited ferroptosis. Furthermore, FXR inhibited ferroptosis in ex vivo mouse hepatocytes and human hepatocytes differentiated from induced pluripotent stem cells. Activation of FXR significantly reduced lipid peroxidation by upregulating the ferroptosis gatekeepers GPX4, FSP1, PPARα, SCD1, and ACSL3. Together, we report that FXR coordinates the expression of ferroptosis-inhibitory regulators to reduce lipid peroxidation, thereby acting as a guardian of ferroptosis.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2041-1723
Relation: https://doi.org/10.1038/s41467-023-42702-8; https://doaj.org/toc/2041-1723; https://doaj.org/article/c8879d0735a7477fa4fa2036c2269a28
DOI: 10.1038/s41467-023-42702-8
الاتاحة: https://doi.org/10.1038/s41467-023-42702-8
https://doaj.org/article/c8879d0735a7477fa4fa2036c2269a28
رقم الانضمام: edsbas.82D3AA23
قاعدة البيانات: BASE
الوصف
تدمد:20411723
DOI:10.1038/s41467-023-42702-8