دورية أكاديمية

Aging impairs cold-induced beige adipogenesis and adipocyte metabolic reprogramming

التفاصيل البيبلوغرافية
العنوان: Aging impairs cold-induced beige adipogenesis and adipocyte metabolic reprogramming
المؤلفون: Corey D Holman, Alexander P Sakers, Ryan P Calhoun, Lan Cheng, Ethan C Fein, Christopher Jacobs, Linus Tsai, Evan D Rosen, Patrick Seale
المصدر: eLife, Vol 12 (2024)
بيانات النشر: eLife Sciences Publications Ltd, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Science
LCC:Biology (General)
مصطلحات موضوعية: beige adipocyte, UCP1, cold exposure, aging, beige adipogenesis, Medicine, Science, Biology (General), QH301-705.5
الوصف: The energy-burning capability of beige adipose tissue is a potential therapeutic tool for reducing obesity and metabolic disease, but this capacity is decreased by aging. Here, we evaluate the impact of aging on the profile and activity of adipocyte stem and progenitor cells (ASPCs) and adipocytes during the beiging process in mice. We found that aging increases the expression of Cd9 and other fibro-inflammatory genes in fibroblastic ASPCs and blocks their differentiation into beige adipocytes. Fibroblastic ASPC populations from young and aged mice were equally competent for beige differentiation in vitro, suggesting that environmental factors suppress adipogenesis in vivo. Examination of adipocytes by single nucleus RNA-sequencing identified compositional and transcriptional differences in adipocyte populations with aging and cold exposure. Notably, cold exposure induced an adipocyte population expressing high levels of de novo lipogenesis (DNL) genes, and this response was severely blunted in aged animals. We further identified Npr3, which encodes the natriuretic peptide clearance receptor, as a marker gene for a subset of white adipocytes and an aging-upregulated gene in adipocytes. In summary, this study indicates that aging blocks beige adipogenesis and dysregulates adipocyte responses to cold exposure and provides a resource for identifying cold and aging-regulated pathways in adipose tissue.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2050-084X
Relation: https://elifesciences.org/articles/87756; https://doaj.org/toc/2050-084X
DOI: 10.7554/eLife.87756
URL الوصول: https://doaj.org/article/a87d04754b664275933a128e3f2ac78b
رقم الأكسشن: edsdoj.87d04754b664275933a128e3f2ac78b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2050084X
DOI:10.7554/eLife.87756