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. 2001 Oct 15;194(8):1111–1122. doi: 10.1084/jem.194.8.1111

Table 1.

TREM-2–dependent Regulation of Cell Surface Activation Markers

F(ab′)2 anti–TREM-1 F(ab′)2 anti–TREM-2 LPS
TREM-2 112.23 3.45 7.1
MHC class I 67.8 65.3 107.1
MHC class II 119.12 278.65 454.67
CD40 171.35 598.6 635.89
CD80 32.1 39.4 104.6
CD86/B7.2 14.04 387.91 683.56
CCR5 12.95 13.56 3.12
CCR6 3.68 3.45 4.01
CCR7 6.82 21.98 12.45
CXCR4 5.13 4.56 17.8
CD11a 10.92 6.78 13.72
CD11b 53.9 65.7 23.1
CD11c 91.1 65.7 123.5
CD29 38.22 37.56 37.5
CD41 4.54 4.67 4.39
CD54/ICAM-1 56.87 54.78 271.45
CD61 4.95 5.03 4.21
CD103 3.63 3.96 3.26
Mannose-R 81.8 82.9 30.9
CD64/FcγR I 9.8 10.1 2.3
CD32/FcγR II 17.21 16.78 2.34
CD89/FcαR 4.54 4.75 4.96
CD35/CR 1 3.94 4.23 3.67
M-CSF-R 14.6 4.23 5.21
GM-CSF-R 15.6 13.7 13.5
CD38 2.5 2.2 43.5
CD83 3.34 3.23 26.7
CD1a 106.76 134.9 87.54

DCs were cultured for 48 h in plates coated with control F(ab′)2, F(ab′)2 anti–TREM-2 mAb, or LPS as indicated in Fig. 6. Cells were subsequently analyzed by flow cytometry for the indicated cell surface molecules. Numerical values indicate specific mean fluorescence intensity after subtraction of the fluorescence detected with an isotype-matched control. The data shown are representative of four independent experiments.