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

Authors

  • 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
Weitere Informationen

Publikationsverlauf

received 09. Oktober 2013
first decision 27. März 2014

accepted 02. April 2014

Publikationsdatum:
16. Mai 2014 (online)

Preview

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.