Temporal phenotypic features distinguish polarized macrophages in vitro

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Abstract

Macrophages are important in vascular inflammation and environmental factors influence macrophage plasticity. Macrophage transitions into pro-inflammatory (M1) or anti-inflammatory (M2) states have been defined predominately by measuring cytokines in culture media (CM). However, temporal relationships between cellular and secreted cytokines have not been established. We measured phenotypic markers and cytokines in cellular and CM of murine bone marrow-derived macrophages at multiple time points following stimulation with IFN-γ + LPS (M1), IL-4 (M2a) or IL-10 (M2c). Cytokines/proteins in M1-polarized macrophages exhibited two distinct temporal patterns; an early (0.5-3 h), transient increase in cellular cytokines (GM-CSF, KC-GRO, MIP-2, IP-10 and MIP-1β) and a delayed (3-6 h) response that was more sustained [IL-3, regulated on activation normal T cell expressed and secreted (RANTES), and tissue inhibitor of metalloproteinases 1 (TIMP-1)]. M2a-related cytokine/cell markers (IGF-1, Fizz1 and Ym1) were progressively (3-24 h) increased post-stimulation. In addition, novel patterns were observed. First, and unexpectedly, cellular pro-inflammatory chemokines, MCP-1 and MCP-3 but not MCP-5, were comparably increased in M1 and M2a macrophages. Second, Vegfr1 mRNA was decreased in M1 and increased in M2a macrophages. Finally, VEGF-A was increased in the CM of M1 cultures and strikingly reduced in M2a coinciding with increased Vegfr1 expression, suggesting decreased VEGF-A in M2a CM was secondary to increased soluble VEGFR1. In conclusion, macrophage cytokine production and marker expression were temporally regulated and relative levels compared across polarizing conditions were highly dependent upon the timing and location (cellular versus CM) of the sample collection. For most cytokines, cellular production preceded increases in the CM suggesting that cellular regulatory pathways should be studied within 6 h of stimulation. The divergent polarization-dependent expression of Vegfr1 may be essential to controlling VEGF potentially regulating angiogenesis and inflammatory cell infiltration in the vascular niche. The current study expands the repertoire of cytokines produced by polarized macrophages and provides insights into the dynamic regulation of macrophage polarization and resulting cytokines, proteins and gene expression that influence vascular inflammation.

Original languageEnglish (US)
Pages (from-to)161-176
Number of pages16
JournalAutoimmunity
Volume48
Issue number3
DOIs
StatePublished - May 1 2015

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Macrophages
Cytokines
Culture Media
Vascular Endothelial Growth Factor A
Blood Vessels
In Vitro Techniques
Inflammation
Tissue Inhibitor of Metalloproteinase-1
Interleukin-3
Granulocyte-Macrophage Colony-Stimulating Factor
Insulin-Like Growth Factor I
Chemokines
Interleukin-4
Interleukin-10
Proteins
Anti-Inflammatory Agents
T-Lymphocytes
Gene Expression
Messenger RNA

Keywords

  • Chemokine
  • Cytokine
  • Macrophage
  • Polarization
  • Temporal

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

Cite this

Temporal phenotypic features distinguish polarized macrophages in vitro. / Melton, David W.; Mcmanus, Linda M; Gelfond, Jonathan A; Shireman, Paula K.

In: Autoimmunity, Vol. 48, No. 3, 01.05.2015, p. 161-176.

Research output: Contribution to journalArticle

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