Comparison of the pro-inflammatory potential of monocytes from healthy adults and those with peripheral arterial disease using an in vitro culture model
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Luu, N. T.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Luu, N. T.
Madden, J.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Madden, J.
Calder, P. C.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Calder, P. C.
Grimble, R. F.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Grimble, R. F.
Shearman, C. P.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Shearman, C. P.
Chan, T.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Chan, T.
Tull, S. P.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Tull, S. P.
Dastur, N.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Dastur, N.
Rainger, G. E.
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机构:Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Rainger, G. E.
Nash, G. B.
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Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
Nash, G. B.
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机构:
[1] Univ Birmingham, Sch Med, Dept Physiol, Ctr Cardiovasc Sci, Birmingham B15 2TT, W Midlands, England
[2] Univ Southampton, Sch Med, Inst Human Nutr, Southampton SO16 7PX, Hants, England
We adapted a monocyte:endothelial cell co-culture model to investigate the pro-inflammatory potential of monocytes from patients with peripheral arterial disease (PAD). Isolated monocytes were cultured with human umbilical vein endothelial cells (HUVEC) for 24 h, after which the ability of the HUVEC to recruit flowing neutrophils was tested. Development of a usable protocol required comparisons of primary HUVEC with cells that had been passaged and/or frozen and thawed, evaluation of optimal culture media and comparison of monocytes from freshly drawn and stored blood. We found, for instance, that expansion of HUVEC was assisted by inclusion of hydrocortisone, but this agent was withdrawn before the test phase because it reduced responses of HUVEC. Using the optimal practical protocol, we found great variation in the ability of monocytes from different donors to cause neutrophil adhesion. Slightly more (similar to 20%) monocytes from patients with PAD adhered to HUVEC than monocytes from healthy controls, and the monocytes from PAD patients induced similar to 70% greater subsequent adhesion of neutrophils. Thus, we developed a functional model of inflammatory potential usable in clinically-related studies and found that patients with PAD had circulating monocytes with greater than normal ability to activate endothelial cells. (c) 2006 Elsevier Ireland Ltd. All rights reserved.