A link between diabetes and atherosclerosis: Glucose regulates expression of CD36 at the level of translation

被引:212
作者
Griffin, E [1 ]
Re, A [1 ]
Hamel, N [1 ]
Fu, CZ [1 ]
Bush, H [1 ]
McCaffrey, T [1 ]
Asch, AS [1 ]
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
D O I
10.1038/89969
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
Both the risk and the rate of development of atherosclerosis are increased in diabetics, but the mechanisms involved are unknown. Here we report a glucose-mediated increase in CD36 mRNA translation efficiency that results in increased expression of the macrophage scavenger receptor CD36. Expression of CD36 was increased in endarterectomy lesions from patients with a history of hyperglycemia. Macrophages that were differentiated from human peripheral blood monocytes in the presence of high glucose concentrations showed increased expression of cell-surface CD36 secondary to an increase in translational efficiency of CD36 mRNA. We obtained similar data from primary cells isolated from human vascular lesions, and we found that glucose sensitivity is a function of ribosomal reinitiation following translation of an upstream open reading frame (uORF). Increased translation of macrophage CD36 transcript under high glucose conditions provides a mechanism for accelerated atherosclerosis in diabetics.
引用
收藏
页码:840 / 846
页数:7
相关论文
共 44 条
[1]   SUPPRESSION OF RIBOSOMAL REINITIATION AT UPSTREAM OPEN READING FRAMES IN AMINO ACID-STARVED CELLS FORMS THE BASIS FOR GCN4 TRANSLATIONAL CONTROL [J].
ABASTADO, JP ;
MILLER, PF ;
JACKSON, BM ;
HINNEBUSCH, AG .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :486-496
[2]   Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [J].
Aitman, TJ ;
Glazier, AM ;
Wallace, CA ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Al-Majali, KM ;
Trembling, PM ;
Mann, CJ ;
Shoulders, CC ;
Graf, D ;
St Lezin, E ;
Kurtz, TW ;
Kren, V ;
Pravenec, M ;
Ibrahimi, A ;
Abumrad, NA ;
Stanton, LW ;
Scott, J .
NATURE GENETICS, 1999, 21 (01) :76-83
[3]   Glucose depletion rapidly inhibits translation initiation in yeast [J].
Ashe, MP ;
De Long, SK ;
Sachs, AB .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :833-848
[4]   PPARγ is required for placental, cardiac, and adipose tissue development [J].
Barak, Y ;
Nelson, MC ;
Ong, ES ;
Jones, YZ ;
Ruiz-Lozano, P ;
Chien, KR ;
Koder, A ;
Evans, RM .
MOLECULAR CELL, 1999, 4 (04) :585-595
[5]   Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension [J].
Barroso, I ;
Gurnell, M ;
Crowley, VEF ;
Agostini, M ;
Schwabe, JW ;
Soos, MA ;
Maslen, GL ;
Williams, TDM ;
Lewis, H ;
Schafer, AJ ;
Chatterjee, VKK ;
O'Rahilly, S .
NATURE, 1999, 402 (6764) :880-883
[6]   MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITIN MESSENGER-RNA IN A FAMILY WITH DOMINANT HYPERFERRITINEMIA AND CATARACT [J].
BEAUMONT, C ;
LENEUVE, P ;
DEVAUX, I ;
SCOAZEC, JY ;
BERTHIER, M ;
LOISEAU, MN ;
GRANDCHAMP, B ;
BONNEAU, D .
NATURE GENETICS, 1995, 11 (04) :444-446
[7]   ATHEROSCLEROSIS - BASIC MECHANISMS - OXIDATION, INFLAMMATION, AND GENETICS [J].
BERLINER, JA ;
NAVAB, M ;
FOGELMAN, AM ;
FRANK, JS ;
DEMER, LL ;
EDWARDS, PA ;
WATSON, AD ;
LUSIS, AJ .
CIRCULATION, 1995, 91 (09) :2488-2496
[8]   Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis [J].
Boring, L ;
Gosling, J ;
Cleary, M ;
Charo, IF .
NATURE, 1998, 394 (6696) :894-897
[9]   CART classification of human 5′ UTR sequences [J].
Davuluri, RV ;
Suzuki, Y ;
Sugano, S ;
Zhang, MQ .
GENOME RESEARCH, 2000, 10 (11) :1807-1816
[10]   Reconstitution of insulin-sensitive glucose transport in fibroblasts requires expression of both PPARγ and C/EBPα [J].
El-Jack, AK ;
Hamm, JK ;
Pilch, PF ;
Farmer, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) :7946-7951