PPAR α does not suppress muscle - associated gene expression in brown adipocytes
نویسندگان
چکیده
Brown adipocytes and myocytes develop from a common adipomyocyte precursor. PPARα is a nuclear receptor important for lipid and glucose metabolism. It has been suggested that in brown adipose tissue, PPARα represses the expression of muscle-associated genes, in this way potentially acting to determinate cell fate in brown adipocytes. To further understand the possible role of PPARα in these processes, we measured muscle-associated gene expression in brown adipose tissue and brown adipocytes from PPARα-ablated mice, including structural genes (Mylpf, Tpm2, Myl3 and MyHC), regulatory genes (myogenin, Myf5 and MyoD) and a myomir ((miR-206), as well as genes that are part of the brown adipocyte signature (Tbx15, Meox2, Zic1 and Lhx8). However, we report here that in our hands the expression of these genes was not influenced by the presence or absence of PPARα, nor by the PPARα activator Wy-14,643. Thus, it would not seem that PPARα plays a significant role in the regulation of the bifurcation of the adipomyocyte precursor into a brown adipocyte or myocyte phenotype; particulary, it would not seem that PPARα represses muscle-associated genes.
منابع مشابه
Peroxisome proliferator-activated receptors-α and -γ, and cAMP-mediated pathways, control retinol-binding protein-4 gene expression in brown adipose tissue.
Retinol binding protein-4 (RBP4) is a serum protein involved in the transport of vitamin A. It is known to be produced by the liver and white adipose tissue. RBP4 release by white fat has been proposed to induce insulin resistance. We analyzed the regulation and production of RBP4 in brown adipose tissue. RBP4 gene expression is induced in brown fat from mice exposed to cold or treated with per...
متن کاملDifferential actions of PPAR-α and PPAR-β/δ on beige adipocyte formation: A study in the subcutaneous white adipose tissue of obese male mice
BACKGROUND AND AIMS Obesity compromises adipocyte physiology. PPARs are essential to adipocyte plasticity, but its isolated role in the browning phenomenon is not clear. This study aimed to examine whether activation of PPAR-α or PPAR-β/δ could induce beige cell depots in the subcutaneous white adipose tissue of diet-induced obese mice. MATERIAL AND METHODS Sixty animals were randomly assigne...
متن کاملبیان ژنPPARγ در سلولهای چربی تمایز یافته از سلولهای بنیادی مزانشیمی مغز استخوان انسانی
Background and Aim: Obesity is now considered as one of the main risk factors of certain known diseases such as cardio-vascular diseases, non- insulin-dependent diabetes, and common cancers. Moreover, the increase of white fat tissue is known as a main factor in the obesity process, in terms of physiology and pathology. Therefore, the understanding of adipocytes differentiation processes is cru...
متن کاملFollistatin promotes adipocyte differentiation, browning, and energy metabolism[S]
Follistatin (Fst) functions to bind and neutralize the activity of members of the transforming growth factor-β superfamily. Fst has a well-established role in skeletal muscle, but we detected significant Fst expression levels in interscapular brown and subcutaneous white adipose tissue, and further investigated its role in adipocyte biology. Fst expression was induced during adipogenic differen...
متن کاملPPARα and Sirt1 Mediate Erythropoietin Action in Increasing Metabolic Activity and Browning of White Adipocytes to Protect Against Obesity and Metabolic Disorders
Erythropoietin (EPO) has shown beneficial effects in the regulation of obesity and metabolic syndrome; however, the detailed mechanism is still largely unknown. Here, we created mice with adipocyte-specific deletion of EPO receptor. These mice exhibited obesity and decreased glucose tolerance and insulin sensitivity, especially when fed a high-fat diet. Moreover, EPO increased oxidative metabol...
متن کامل