2013 Fiscal Year Final Research Report
Screening of novel factors for those regulating fat mass under the nutrient excess state
Project/Area Number |
24659442
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Single-year Grants |
Research Field |
Metabolomics
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Research Institution | Gunma University |
Principal Investigator |
IZUMI Tetsuro 群馬大学, 生体調節研究所, 教授 (00212952)
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Project Period (FY) |
2012-04-01 – 2014-03-31
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Keywords | 脂肪蓄積 / 脂肪代謝 / 脂肪細胞 / 肥満 / 糖尿病 |
Research Abstract |
We recently discovered a novel signaling pathway involving ALK7, one of the type I TGFbeta receptors, which increases both the adipocyte size and lipid content by suppressing lipolysis. To understand the function and regulation of this pathway, it is essential to identify its unknown ligands of this orphan receptor. For this purpose, 33 mammalian TGFbeta family members were screened for those upregulated under a nutrient excess state. As a result, four members were found to be upregulated. Furthermore, three of them showed ligand activities to increase gene expression through ALK7 in cultured cells. All the three candidate ligands were highly expressed in adipose tissue, although each of them was expressed in different kinds of cells. These results suggest that these ALK7 ligands function in an autocrine or paracrine manner to regulate the lipid metabolism and content of mature adipocytes.
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Research Products
(12 results)
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[Journal Article] TFE3 controls lipid metabolism in adipose tissue of male mice by suppressing lipolysis and thermogenesis2013
Author(s)
Fujimoto Y, Nakagawa Y, Satoh A, Okuda K, Shingyouchi A, Naka A, Matsuzaka T, Iwasaki H, Kobayashi K, Yahagi N , Shimada M, Yatoh S, Suzuki H, Yogosawa S, Izumi T, Sone H, Urayama O, Yamada N, and Shimano H.
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Journal Title
Endocrinology
Volume: 154
Pages: 3577-3588
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