Exp Clin Endocrinol Diabetes 2014; 122(08): 463-468
DOI: 10.1055/s-0034-1374600
Article
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Regulation of ATP-binding Cassette Transporters and Cholesterol Efflux by Glucose in Primary Human Monocytes and Murine Bone Marrow-derived Macrophages

N. L. Spartano
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
S. Lamon-Fava
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
N. R. Matthan
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
J. Ronxhi
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
A. S. Greenberg
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
M. S. Obin
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
,
A. H. Lichtenstein
1   Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, United States
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Publikationsverlauf

received 09. Oktober 2013
first decision 27. März 2014

accepted 02. April 2014

Publikationsdatum:
16. Mai 2014 (online)

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Abstract

Purpose:

Individuals with type 2 diabetes mellitus are at increased risk of developing atherosclerosis. This may be partially attributable to suppression of macrophage ATP-binding cassette (ABC) transporter mediated cholesterol efflux by sustained elevated blood glucose concentrations. 2 models were used to assess this potential relationship: human monocytes/leukocytes and murine bone marrow-derived macrophages (BMDM).

Methods:

10 subjects (4 F/6 M, 50–85 years, BMI 25–35 kg/m²) underwent an oral glucose challenge. Baseline and 1- and 2-h post-challenge ABC-transporter mRNA expression was determined in monocytes, leukocytes and peripheral blood mononuclear cells (PBMC). In a separate study, murine-BMDM were exposed to 5 mmol/L D-glucose (control) or additional 20 mmol/L D- or L-glucose and 25 ug/mL oxidized low density lipoprotein (oxLDL). High density lipoprotein (HDL)-mediated cholesterol efflux and ABC-transporter (ABCA1 and ABCG1) expression were determined.

Results:

Baseline ABCA1and ABCG1 expression was lower (>50%) in human monocytes and PBMC than leukocytes (p<0.05). 1 h post-challenge leukocyte ABCA1 and ABCG1 expression increased by 37% and 30%, respectively (p<0.05), and began to return to baseline thereafter. There was no significant change in monocyte ABC-transporter expression. In murine BMDM, higher glucose concentrations suppressed HDL-mediated cholesterol efflux (10%; p<0.01) without significantly affecting ABCA1 and ABCG1 expression. Data demonstrate that leukocytes are not a reliable indicator of monocyte ABC-transporter expression.

Conclusions:

Human monocyte ABC-transporter gene expression was unresponsive to a glucose challenge. Correspondingly, in BMDM, hyperglycemia attenuated macrophage cholesterol efflux in the absence of altered ABC-transporter expression, suggesting that hyperglycemia, per se, suppresses cholesterol transporter activity. This glucose-related impairment in cholesterol efflux may potentially contribute to diabetes-associated atherosclerosis.