Recently, there has been great attention given to the possibility of combating obesity by targeting brown fat activity or increasing differentiation of brown adipocytes in white fat depots through a process termed 'browning'. Sympathetic innervation of brown and white adipose tissues provides adrenergic input that drives thermogenesis and regulates fatty acid metabolism, as well as stimulating adipogenesis of recruitable brown adipocyte tissue (rBAT, also known as beige or brite) in white fat. Other factors acting in an endocrine or autocrine/paracrine manner in adipose tissue may also stimulate browning. There have been significant recent advances in understanding the mechanisms of increasing adipose tissue energy expenditure, as well as how brown adipocytes appear in white fat depots, including via de novo adipogenesis from tissue precursor cells. In this article, we integrate this new knowledge with a historical perspective on the discovery of 'browning'. We also provide an overview of constitutive BAT vs rBAT in mouse and human.
Keyphrases
- adipose tissue
- high fat diet induced
- insulin resistance
- high fat diet
- fatty acid
- induced apoptosis
- gene expression
- type diabetes
- healthcare
- endothelial cells
- working memory
- cell proliferation
- small molecule
- physical activity
- weight loss
- skeletal muscle
- high throughput
- cell cycle arrest
- cell death
- induced pluripotent stem cells
- pluripotent stem cells
- oxidative stress
- pi k akt