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Total 3 results found since Jan 2013.

The mitochondrial protein PGAM5 suppresses energy consumption in brown adipocytes by repressing expression of uncoupling protein 1 Metabolism
Accumulating evidence suggests that brown adipose tissue (BAT) is a potential therapeutic target for managing obesity and related diseases. PGAM family member 5, mitochondrial serine/threonine protein phosphatase (PGAM5), is a protein phosphatase that resides in the mitochondria and regulates many biological processes, including cell death, mitophagy, and immune responses. Because BAT is a mitochondria-rich tissue, we have hypothesized that PGAM5 has a physiological function in BAT. We previously reported that PGAM5-knockout (KO) mice are resistant to severe metabolic stress. Importantly, lipid accumulation is suppressed i...
Source: Journal of Biological Chemistry - April 23, 2020 Category: Chemistry Authors: Sho Sugawara, Yusuke Kanamaru, Shiori Sekine, Lila Maekawa, Akinori Takahashi, Tadashi Yamamoto, Kengo Watanabe, Takao Fujisawa, Kazuki Hattori, Hidenori Ichijo Tags: Cell Biology Source Type: research

Catecholamines Regulate Iron Homeostasis Metabolism
This study reveals epinephrine and norepinephrine as novel regulators of cellular iron homeostasis.
Source: Journal of Biological Chemistry - March 20, 2015 Category: Chemistry Authors: Tapryal, N., Vivek G, V., Mukhopadhyay, C. K. Tags: Gene Regulation Source Type: research

SMAD3 Suppresses FNDC5 and PGC-1{alpha} in Skeletal Muscle Signal Transduction
Beige adipose cells are a distinct and inducible type of thermogenic fat cell that express the mitochondrial uncoupling protein-1 and thus represent a powerful target for treating obesity. Mice lacking the TGF-β effector protein SMAD3 are protected against diet-induced obesity because of browning of their white adipose tissue (WAT), leading to increased whole body energy expenditure. However, the role SMAD3 plays in WAT browning is not clearly understood. Irisin is an exercise-induced skeletal muscle hormone that induces WAT browning similar to that observed in SMAD3-deficient mice. Together, these observations suggested ...
Source: Journal of Biological Chemistry - March 20, 2015 Category: Chemistry Authors: Tiano, J. P., Springer, D. A., Rane, S. G. Tags: Cell Biology Source Type: research