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Comparison of the pro-inflammatory potential of monocytes from healthy adults and those with peripheral arterial disease using an in vitro culture model

Comparison of the pro-inflammatory potential of monocytes from healthy adults and those with peripheral arterial disease using an in vitro culture model
Comparison of the pro-inflammatory potential of monocytes from healthy adults and those with peripheral arterial disease using an in vitro culture model
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 24h, 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 We found, for instance, that expansion of HUVEC was assisted by inclusion of hydrocortisone, but this agent was withdrawn before the test phase because it reduced responses of HUVEC.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 ( approximately 20%) monocytes from patients with PAD adhered to HUVEC than monocytes from healthy controls, and the monocytes from PAD patients induced approximately 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
human, endothelial cells, hydrocortisone, blood, cells, adult, research, tumor necrosis factor-alpha, cultured, peripheral vascular diseases, disease, neutrophils, physiology, biosynthesis, monocytes, cytokines, neutrophil activation, umbilical veins, culture media, neutrophil infiltration, humans, immunology
0021-9150
259-268
Luu, N.T.
95af76c9-a70c-4b0e-87e2-e70f7f0ff2fd
Madden, J.
0771e352-d432-41ea-8a7e-4704c1efca46
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Grimble, R.F.
3100e4d2-8f29-4ca6-a95d-38a6a764865f
Shearman, C.P.
cf4d6317-f54d-4ab3-ba49-c6797897bbcf
Chan, T.
5dd3d19b-381c-42f0-8d65-403a46b2b87b
Tull, S.P.
4fd6df77-1f5c-4ac2-8024-0426c8570163
Dastur, N.
35cd496a-d5e6-45b3-b193-eb54b6ab270e
Rainger, G.E.
0bbadb52-915e-4217-aa9b-e1974eda8031
Nash, G.B.
49c0c507-bd33-432d-8a26-daedcf2ff658
Luu, N.T.
95af76c9-a70c-4b0e-87e2-e70f7f0ff2fd
Madden, J.
0771e352-d432-41ea-8a7e-4704c1efca46
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Grimble, R.F.
3100e4d2-8f29-4ca6-a95d-38a6a764865f
Shearman, C.P.
cf4d6317-f54d-4ab3-ba49-c6797897bbcf
Chan, T.
5dd3d19b-381c-42f0-8d65-403a46b2b87b
Tull, S.P.
4fd6df77-1f5c-4ac2-8024-0426c8570163
Dastur, N.
35cd496a-d5e6-45b3-b193-eb54b6ab270e
Rainger, G.E.
0bbadb52-915e-4217-aa9b-e1974eda8031
Nash, G.B.
49c0c507-bd33-432d-8a26-daedcf2ff658

Luu, N.T., Madden, J., Calder, P.C., Grimble, R.F., Shearman, C.P., Chan, T., Tull, S.P., Dastur, N., Rainger, G.E. and Nash, G.B. (2007) Comparison of the pro-inflammatory potential of monocytes from healthy adults and those with peripheral arterial disease using an in vitro culture model. Atherosclerosis, 193 (2), 259-268. (doi:10.1016/j.atherosclerosis.2006.08.050).

Record type: Article

Abstract

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 24h, 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 ( approximately 20%) monocytes from patients with PAD adhered to HUVEC than monocytes from healthy controls, and the monocytes from PAD patients induced approximately 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

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More information

Submitted date: July 2005
Published date: August 2007
Keywords: human, endothelial cells, hydrocortisone, blood, cells, adult, research, tumor necrosis factor-alpha, cultured, peripheral vascular diseases, disease, neutrophils, physiology, biosynthesis, monocytes, cytokines, neutrophil activation, umbilical veins, culture media, neutrophil infiltration, humans, immunology
Organisations: Dev Origins of Health & Disease

Identifiers

Local EPrints ID: 44242
URI: http://eprints.soton.ac.uk/id/eprint/44242
ISSN: 0021-9150
PURE UUID: 18d56519-c6ed-4d17-af2f-cd3407ff2912
ORCID for P.C. Calder: ORCID iD orcid.org/0000-0002-6038-710X

Catalogue record

Date deposited: 21 Feb 2007
Last modified: 16 Mar 2024 02:51

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Contributors

Author: N.T. Luu
Author: J. Madden
Author: P.C. Calder ORCID iD
Author: R.F. Grimble
Author: C.P. Shearman
Author: T. Chan
Author: S.P. Tull
Author: N. Dastur
Author: G.E. Rainger
Author: G.B. Nash

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