| Literature DB >> 24969110 |
Satoshi Nishimura1, Mika Nagasaki2, Shinichi Okudaira3, Junken Aoki3, Tsukasa Ohmori4, Ryunosuke Ohkawa5, Kazuhiro Nakamura5, Koji Igarashi6, Hiroshi Yamashita7, Koji Eto8, Kansei Uno2, Naoto Hayashi9, Takashi Kadowaki10, Issei Komuro7, Yutaka Yatomi5, Ryozo Nagai4.
Abstract
Body weight is tightly regulated by food intake and energy dissipation, and obesity is related to decreased energy expenditure (EE). Herein, we show that nucleotide pyrophosphatase/phosphodiesterase 2 (ENPP2, autotaxin) is an adipose-derived, secreted enzyme that controls adipose expansion, brown adipose tissue (BAT) function, and EE. In mice, Enpp2 was highly expressed in visceral white adipose tissue and BAT and is downregulated in hypertrophied adipocytes/adipose tissue. Enpp2(+/-) mice and adipocyte-specific Enpp2 knockout mice fed a high-fat diet showed smaller body weight gains and less insulin resistance than control mice fed the same diet. BAT was functionally more active and EE was increased in Enpp2-deficient mice. In humans, ENPP2 expression in subcutaneous fat and ENPP2 levels in serum were reduced in obese subjects. Taken together, our results establish ENPP2 as an adipose-derived, secreted enzyme that regulates adipose obesity and systemic metabolism. They also suggest ENPP2 could be a useful therapeutic target for the treatment of metabolic disease.Entities:
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Year: 2014 PMID: 24969110 DOI: 10.2337/db13-1694
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461