肌肉PGC-1α过度表达驱动代谢物分泌增强皮下脂肪细胞棕色化
Caterina Miro1, Ciro Menale1, Lucia Acampora1
1Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy.
Journal of cellular physiology
|December 16, 2024
概括
肌肉中的氧酶增殖器激活受体-γ联合激活器-1α (PGC-1α) 激活线粒体,改变代谢物. 这些变化影响脂肪组织 (AT) 细胞分化和色,特别是在皮下AT细胞中.
科学领域:
- 骨肌肉和脂肪组织之间的代谢相互作用.
- 线粒体生物发生和功能调节.
- 内分泌和代谢信号通路.
背景情况:
- 肌肉和脂肪组织通过内分泌和生化信号进行通信.
- 越来越多地认识到一种涉及组织之间信号代谢物的代谢网络.
- 过氧酶增殖器激活的受体-γ联合激活剂-1α (PGC-1α) 是肌肉中线粒体生物发生的主调节者,促进转向氧化肌纤维.
研究的目的:
- 调查肌肉纤维过度表达PGC-1α的代谢物分泌特征.
- 为了确定PGC-1α诱导的代谢变化对脂肪组织的影响.
- 阐明由肌肉衍生代谢物影响脂肪组织功能的机制.
主要方法:
- 使用一种肌肉特定的PGC-1α过度表达的小鼠模型 (MCK-PGC-1α).
- 使用核磁共振 (NMR) 分析了血清和肌肉培养介质代谢物概况.
- 评估了改变代谢物对脂肪细胞分化和棕色化 in vitro 和 in vivo 的影响.
主要成果:
- 揭示了MCK-PGC-1α肌肉纤维中各种代谢物的修饰水平,表明代谢激活.
- 证明失调的代谢物水平影响了脂肪细胞分化和脂肪组织色.
- 与内脏WAT相比,观察到对皮下白色脂肪组织 (WAT) 的恶化影响.
结论:
- 证实了PGC-1α在触发骨肌肉中的线粒体功能中的作用.
- 提出了PGC-1α在调节肌肉代谢物产生的新功能.
- 突出了PGC-1α对脂肪组织激活和通过代谢信号的色的影响.
更多相关视频
04:46Differentiation and Imaging of Brown Adipocytes from the Stromal Vascular Fraction of Interscapular Adipose Tissue from Newborn Mice
Published on: February 3, 2023
1.3K
07:07Isolating Brown Adipocytes from Murine Interscapular Brown Adipose Tissue for Gene and Protein Expression Analysis
Published on: March 12, 2021
5.4K
相关概念视频
Cell Specific Gene Expression
13.4K
Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...
13.4K
GPCRs Regulate Adenylyl Cylase Activity
5.3K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.3K
cAMP-dependent Protein Kinase Pathways
6.1K
Cyclic Adenosine Monophosphate (cAMP) is an essential second messenger that activates protein kinase A (PKA) and regulates various biological processes. A single epinephrine molecule binds to GPCR and activates several heterotrimeric G proteins, each stimulating multiple adenylyl cyclase, amplifying the signal, and synthesizing large numbers of cAMP molecules. Small changes in cAMP concentration affect PKA activity. The binding of four cAMP molecules induces a conformational change in PKA,...
6.1K
