Effects of interleukin-15 on lipid oxidation Disposal of an oral [14C]-triolein load

被引:46
作者
Almendro, V [1 ]
Busquets, S [1 ]
Arrieffler, E [1 ]
Carbó, N [1 ]
Figueras, M [1 ]
Fuster, G [1 ]
Argilés, JM [1 ]
López-Soriano, FJ [1 ]
机构
[1] Univ Barcelona, Fac Biol, Canc Res Grp, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2006年 / 1761卷 / 01期
关键词
IL-15; lipid metabolism; skeletal muscle; liver; PPAR;
D O I
10.1016/j.bbalip.2005.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin 15 (IL-15) has previously been shown to have important effects on lipid metabolism in adipose tissue, particularly influencing the rate of the de novo fatty acid synthesis. The results presented here show that chronic administration to rats (100 mu g/kg body weight) has important effects on the metabolic fate of an exogenous [C-14]-triolein load, decreasing the incorporation of lipid into adipose tissue and significantly increasing the total (CO2)-C-14 formation from [C-14]-triolein. Skeletal muscle and possibly liver seem to be the main organs involved in the action of IL-15 on lipid oxidation, since the presence of the cytokine in incubated EDL muscle with [C-14]-palmitic acid increased (CO2)-C-14 formation by 39%. Concerning the mechanism, the results Suggest that the transport of fatty acids into mitochondria could be involved in the action of IL-15 since the cytokine clearly increases the presence of L-CPT-I and CPT-II in liver tissue. In addition, IL-15 treatment resulted in a significant increment in the gene expression of PPAR delta, a transcription factor clearly related with lipid catabolism in many tissues. Altogether, the results presented here suggest that IL-15 alters exogenous lipid partitioning, limiting adipose tissue uptake and favouring oxidation. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 25 条
[1]   Interleukin-2 receptor common gamma-chain signaling cytokines regulate activated T cell apoptosis in response to growth factor withdrawal: Selective induction of anti-apoptotic (bcl-2, bcl-x(L)) but not pro-apoptotic (bax, bcl-x(S)) gene expression [J].
Akbar, AN ;
Borthwick, NJ ;
Wickremasinghe, RG ;
Panayiotidis, P ;
Pilling, D ;
Bofill, M ;
Krajewski, S ;
Reed, JC ;
Salmon, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (02) :294-299
[2]   Effects of interleukin-15 (IL-15) on adipose tissue mass in rodent obesity models:: evidence for direct IL-15 action on adipose tissue [J].
Alvarez, B ;
Carbó, N ;
López-Soriano, J ;
Drivdahl, RH ;
Busquets, S ;
López-Soriano, FJ ;
Argilés, JM ;
Quinn, LS .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1570 (01) :33-37
[3]  
ARMITAGE RJ, 1995, J IMMUNOL, V154, P483
[4]   Effects of peroxisome proliferator-activated receptor δ on placentation, adiposity, and colorectal cancer [J].
Barak, Y ;
Liao, D ;
He, WM ;
Ong, ES ;
Nelson, MC ;
Olefsky, JM ;
Boland, R ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :303-308
[5]  
Busquets S, 2000, J CELL PHYSIOL, V184, P380, DOI 10.1002/1097-4652(200009)184:3<380::AID-JCP13>3.0.CO
[6]  
2-F
[7]   Branched-chain amino acids:: A role in skeletal muscle proteolysis in catabolic states? [J].
Busquets, S ;
Alvarez, B ;
López-Soriano, FJ ;
Argilés, JM .
JOURNAL OF CELLULAR PHYSIOLOGY, 2002, 191 (03) :283-289
[8]   Interleukin-15 antagonizes muscle protein waste in tumour-bearing rats [J].
Carbo, N. ;
Lopez-Soriano, J. ;
Costelli, P. ;
Busquets, S. ;
Alvarez, B. ;
Baccino, F. M. ;
Quinn, L. S. ;
Lopez-Soriano, F. J. ;
Argiles, J. M. .
BRITISH JOURNAL OF CANCER, 2000, 83 (04) :526-531
[9]   Interleukin-15 mediates reciprocal regulation of adipose and muscle mass:: A potential role in body weight control [J].
Carbó, N ;
López-Soriano, J ;
Costelli, P ;
Alvarez, B ;
Busquets, S ;
Baccino, FM ;
Quinn, LS ;
López-Soriano, FJ ;
Argilés, JM .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1526 (01) :17-24
[10]   INTERLEUKIN (IL)-15 IS A NOVEL CYTOKINE THAT ACTIVATES HUMAN NATURAL-KILLER-CELLS VIA COMPONENTS OF THE IL-2 RECEPTOR [J].
CARSON, WE ;
GIRI, JG ;
LINDEMANN, MJ ;
LINETT, ML ;
AHDIEH, M ;
PAXTON, R ;
ANDERSON, D ;
EISENMANN, J ;
GRABSTEIN, K ;
CALIGIURI, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1395-1403