肿瘤抑制因子
脂肪组织
内分泌学
内科学
脂肪细胞
脂肪组织巨噬细胞
脂解
串扰
免疫系统
生物
白色脂肪组织
骨骼肌
细胞生物学
炎症
医学
白细胞介素6
免疫学
物理
光学
作者
Lucile Dollet,Lars Lundell,Alexander V. Chibalin,Logan A. Pendergrast,Nicolas Pillon,Elizabeth Lansbury,Merve Elmastas,Scott Frendo‐Cumbo,Jutta Jalkanen,Thaís de Castro Barbosa,Daniel T. Cervone,Kenneth Caidahl,Oksana Dmytriyeva,Atul S. Deshmukh,Romain Barrès,Mikael Rydén,Harriet Wallberg-Henriksson,Juleen R. Zierath,Anna Krook
标识
DOI:10.1016/j.xcrm.2023.101348
摘要
The discovery of exercise-regulated circulatory factors has fueled interest in organ crosstalk, especially between skeletal muscle and adipose tissue, and the role in mediating beneficial effects of exercise. We studied the adipose tissue transcriptome in men and women with normal glucose tolerance or type 2 diabetes following an acute exercise bout, revealing substantial exercise- and time-dependent changes, with sustained increase in inflammatory genes in type 2 diabetes. We identify oncostatin-M as one of the most upregulated adipose-tissue-secreted factors post-exercise. In cultured human adipocytes, oncostatin-M enhances MAPK signaling and regulates lipolysis. Oncostatin-M expression arises predominantly from adipose tissue immune cell fractions, while the corresponding receptors are expressed in adipocytes. Oncostatin-M expression increases in cultured human Thp1 macrophages following exercise-like stimuli. Our results suggest that immune cells, via secreted factors such as oncostatin-M, mediate a crosstalk between skeletal muscle and adipose tissue during exercise to regulate adipocyte metabolism and adaptation.
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