دورية أكاديمية

Characteristic ERK1/2 signaling dynamics distinguishes necroptosis from apoptosis

التفاصيل البيبلوغرافية
العنوان: Characteristic ERK1/2 signaling dynamics distinguishes necroptosis from apoptosis
المؤلفون: François Sipieter, Benjamin Cappe, Aymeric Leray, Elke De Schutter, Jolien Bridelance, Paco Hulpiau, Guy Van Camp, Wim Declercq, Laurent Héliot, Pierre Vincent, Peter Vandenabeele, Franck B. Riquet
المصدر: iScience, Vol 24, Iss 9, Pp 103074- (2021)
بيانات النشر: Elsevier, 2021.
سنة النشر: 2021
المجموعة: LCC:Science
مصطلحات موضوعية: Biological sciences, Biomolecular engineering, Cell biology, Science
الوصف: Summary: ERK1/2 involvement in cell death remains unclear, although many studies have demonstrated the importance of ERK1/2 dynamics in determining cellular responses. To untangle how ERK1/2 contributes to two cell death programs, we investigated ERK1/2 signaling dynamics during hFasL-induced apoptosis and TNF-induced necroptosis in L929 cells. We observed that ERK1/2 inhibition sensitizes cells to apoptosis while delaying necroptosis. By monitoring ERK1/2 activity by live-cell imaging using an improved ERK1/2 biosensor (EKAR4.0), we reported differential ERK1/2 signaling dynamics between cell survival, apoptosis, and necroptosis. We also decrypted a temporally shifted amplitude- and frequency-modulated (AM/FM) ERK1/2 activity profile in necroptosis versus apoptosis. ERK1/2 inhibition, which disrupted ERK1/2 signaling dynamics, prevented TNF and IL-6 gene expression increase during TNF-induced necroptosis. Using an inducible cell line for activated MLKL, the final executioner of necroptosis, we showed ERK1/2 and its distinctive necroptotic ERK1/2 activity dynamics to be positioned downstream of MLKL.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2589-0042
Relation: http://www.sciencedirect.com/science/article/pii/S2589004221010427; https://doaj.org/toc/2589-0042
DOI: 10.1016/j.isci.2021.103074
URL الوصول: https://doaj.org/article/68a7ef265975416abc55a7795e1aa47c
رقم الأكسشن: edsdoj.68a7ef265975416abc55a7795e1aa47c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25890042
DOI:10.1016/j.isci.2021.103074