Abstract
Local dysregulation of iron metabolism is suggested to contribute to atherosclerotic lesion development through hemoglobin scavenging pathways. We evaluated the effects of CD163-mediated uptake of hemoglobin-haptoglobin (HbHp) complexes on surface CD163 and intracellular heme oxygenase-1 expression and the secretion of pro- and antiinflammatory cytokines by macrophages. We found that increased availability of HbHp complexes triggers the upregulation of surface CD163, and also results in a dose-dependent secretion of IL-6 and IL-10.
(c) 2006 International Society for Analytical Cytology.
MeSH terms
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Antigens, CD / metabolism*
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Antigens, Differentiation, Myelomonocytic / metabolism*
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CD163 Antigen
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Flow Cytometry
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Gene Expression / drug effects
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Gene Expression / genetics
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Haptoglobins / pharmacokinetics*
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Haptoglobins / pharmacology
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Heme Oxygenase-1 / genetics
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Heme Oxygenase-1 / metabolism
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Hemoglobins / pharmacokinetics*
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Hemoglobins / pharmacology
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Humans
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Interleukin-10 / metabolism
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Interleukin-6 / metabolism
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Interleukins / metabolism*
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Macrophages / drug effects
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Macrophages / metabolism*
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Monocytes / drug effects
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Monocytes / metabolism*
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Receptors, Cell Surface / metabolism*
Substances
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Antigens, CD
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Antigens, Differentiation, Myelomonocytic
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CD163 Antigen
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Haptoglobins
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Hemoglobins
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Interleukin-6
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Interleukins
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RNA, Messenger
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Receptors, Cell Surface
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haptoglobin-hemoglobin complex
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Interleukin-10
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HMOX1 protein, human
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Heme Oxygenase-1