Academic Journal

YTHDF1-CLOCK axis contributes to pathogenesis of allergic airway inflammation through LLPS

التفاصيل البيبلوغرافية
العنوان: YTHDF1-CLOCK axis contributes to pathogenesis of allergic airway inflammation through LLPS
المؤلفون: Jing Wang, Yao Zhou, Meng Zhang, Yujiao Wu, Qun Wu, Wen Su, Min Xu, Jinhong Wu, Min Zhang, Jianwei Shuai, Wei Tang, Jiajia Lv, Min Wu, Zhenwei Xia
المصدر: Cell Reports, Vol 43, Iss 3, Pp 113947- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: CP: Molecular biology, CP: Immunology, Biology (General), QH301-705.5
الوصف: Summary: N6-methyladenosine (m6A) modification has been implicated in many cell processes and diseases. YTHDF1, a translation-facilitating m6A reader, has not been previously shown to be related to allergic airway inflammation. Here, we report that YTHDF1 is highly expressed in allergic airway epithelial cells and asthmatic patients and that it influences proinflammatory responses. CLOCK, a subunit of the circadian clock pathway, is the direct target of YTHDF1. YTHDF1 augments CLOCK translation in an m6A-dependent manner. Allergens enhance the liquid-liquid phase separation (LLPS) of YTHDF1 and drive the formation of a complex comprising dimeric YTHDF1 and CLOCK mRNA, which is distributed to stress granules. Moreover, YTHDF1 strongly activates NLRP3 inflammasome production and interleukin-1β secretion leading to airway inflammatory responses, but these phenotypes are abolished by deleting CLOCK. These findings demonstrate that YTHDF1 is an important regulator of asthmatic airway inflammation, suggesting a potential therapeutic target for allergic airway inflammation.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2211-1247
Relation: http://www.sciencedirect.com/science/article/pii/S2211124724002754; https://doaj.org/toc/2211-1247
DOI: 10.1016/j.celrep.2024.113947
URL الوصول: https://doaj.org/article/7b4f93fd66ef451988be73ab197f0dd1
رقم الانضمام: edsdoj.7b4f93fd66ef451988be73ab197f0dd1
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22111247
DOI:10.1016/j.celrep.2024.113947