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Lymphotoxin pReceptor-Dependent Control of Lipid Homeostasis
Oleh:
Lo, James C.
;
Wang, Yugang
;
Tumanov, Alexei V.
;
Bamji, Michelle
;
Yao, Zemin
;
Reardon, Catherine A.
;
Getz, Godfrey S.
;
Fu, Yang-Xin
Jenis:
Article from Bulletin/Magazine
Dalam koleksi:
SCIENCE (keterangan: ada di Proquest) vol. 316 no. 5822 (Apr. 2007)
,
page 285.
Ketersediaan
Perpustakaan FK
Nomor Panggil:
S01.K.2007.04
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Hyperlipidemia, one of the most important risk factors for coronary heart disease, is often associated with inflammation. We identified lymphotoxin (LT) and LIGHT, tumor necrosis factor cytokine family members that are primarily expressed on lymphocytes, as critical regulators of key enzymes that control lipid metabolism. Dysregulation of LIGHT expression on T cells resulted in hypertriglyceridemia and hypercholesterolemia. In low-density lipoprotein receptor-deficient mice, which lack the ability to control lipid levels in the blood, inhibition of LT and LIGHT signaling with a soluble lymphotoxin ~ receptor decoy protein attenuated the dyslipidemia. These results suggest that the immune system directly influences lipid metabolism and that LT modulating agents may represent a novel therapeutic route for the treatment of dyslipidemia.
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