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. 2003 Feb 26;100(5):2426–2431. doi: 10.1073/pnas.0536882100

Table 1.

Characterization of f-MΦ and s-MΦ

Relative fluorescence intensity
f-MΦ s-MΦ
Surface antigens
 MAC-1 78  ± 15 81  ± 12
 HLA-DR 19  ± 5 102  ± 43
 HLA-DQ 21  ± 8 91  ± 27
 CD1a 1 12  ± 4
 CD14 129  ± 27 155  ± 22
 CD34 78  ± 17 18  ± 5
 CD40 51  ± 24 48  ± 19
 CD45 146  ± 24 162  ± 41
 CD83 1 1
Cytokine production
 IL-1β 84  ± 27 83  ± 15
 IL-6 45  ± 20 65  ± 16
 IL-10 9  ± 6 56  ± 9
 IL-12 p70 52  ± 27 54  ± 8
 TNF-α 29  ± 13 65  ± 18
 TNF-RI 25  ± 7 34  ± 15
 TNF-RII 9  ± 4 63  ± 27
Adipocyte markers
 Lipids 14  ± 11 157  ± 12
 Leptin production 23  ± 7 88  ± 16
 PPARγ2 20  ± 6 110  ± 32
Functional indicators
 Phagocytosis 189  ± 21 197  ± 23
 Lymphocyte stimulation, Abs540* 0.76  ± 0.05 0.15  ± 0.03
 Cytotoxicity, % 10  ± 4 70  ± 8

Relative fluorescence intensity was examined by quantitative ratio imaging microscopy. Stimulation of lymphocyte proliferation was performed by using a 10:1 macrophages-to-lymphocytes ratio, and cytotoxicity was performed by using a 5:1 macrophages-to-target cell ratio (10, 12). 

*

Abs540, optical absorbance at 540 nm.