脂肪组织
白色脂肪组织
内分泌学
内科学
脂肪细胞
脂肪生成
生物
脂肪组织巨噬细胞
葡萄糖稳态
胰岛素抵抗
祖细胞
细胞生物学
干细胞
胰岛素
医学
作者
Christine Mund,Anupam Sinha,Anika Aderhold,Ivona Mateska,Eman Hagag,Sofia Traikov,Bettina Gercken,Andrés Soto,Jonathan D. Pollock,Lilli Arndt,Michele Wölk,Natalie S. Werner,Georgia Fodelianaki,Pallavi Subramanian,Kyoung‐Jin Chung,Sylvia Großklaus,Mathias Langner,Mohamed Elgendy,Tatyana Grinenko,Ben Wielockx
标识
DOI:10.1016/j.metabol.2025.156358
摘要
BACKGROUND AND AIMS: Adipose tissue function is integral to systemic metabolic homeostasis. Excessive adipose tissue growth is associated with development of chronic low-grade inflammation and whole body dysmetabolism. The cell metabolic pathways regulating adipose tissue growth and homeostasis are little understood. Here we studied the role of polyamine metabolism in adipose tissue (patho)physiology. METHODS: We generated mice with global and adipocyte progenitor (AP)-specific Antizyme inhibitor 2 (AZIN2) deficiency and performed diet-induced obesity studies. APs were isolated from the subcutaneous and gonadal adipose tissue of mice and cultured. RESULTS: APs committed more efficiently to adipogenesis in vivo and in vitro, and were more prone to senescence compared to wild-type counterparts. Upon diet-induced obesity, global and AP-specific AZIN2 deficiency in mice provoked AP depletion, adipocyte hypertrophy, obesity, inflammation, glucose intolerance and insulin resistance. In human adipose tissue, AZIN2 expression strongly correlated with expression of progenitor markers. CONCLUSIONS: Altogether, we identified AZIN2 as a novel AP marker that regulates AP fate and preserves adipose tissue health.
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