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. Author manuscript; available in PMC: 2013 Dec 14.
Published in final edited form as: J Immunol Methods. 2012 Sep 10;386(1-2):50–59. doi: 10.1016/j.jim.2012.08.018

Table 1.

The effect of different enzyme preparations on the relative mean fluorescence intensity (rMFI)* of leukocyte surface antigens in human stromavascular cells freshly isolated from adipose tissue following a 45–75 min digestion.

Cell population Surface Marker Collagenase I (1 mg/ml) mean (SD)
N=10
Liberase (0.035 mg/ml) mean (SD)
N=8
p value
Leukocytes (CD45pos) CD45 3,771 (553) 3,992 (771) 0.489

Neutrophils (CD15posCD16hi) CD16 123,951 (75,778) 62,066 (43,961) 0.058

Macrophages (CD14posCD206pos) CD14 4,237 (1,892) 4,972 (1,598) 0.146
CD206 6,038 (1,538) 5,143 (1,476) 0.397
CD11c 310 (141) 318 (124) 0.696
CD40 686 (413) 565 (311) 0.502
CD16 738 (671) 1051 (774) 0.372

T lymphocytes (CD3pos) CD3 1,423 (856) 1,664 (831) 0.558
CD4 667 (390) 90 (37) <0.001
CD8 2,389 (1,269) 1,584 (1,139) 0.182

Lymphocytes CD16 21,117 (21,450) 18,476 (16,418) 0.897
*

rMFI was determined by subtracting the MFI of the isotype controls from the MFI for each population identified by a defined gate using specific cell surface markers. MFI itself was obtained using the geometric mean statistic.