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. 2015 Dec 9;21(1):924–936. doi: 10.2119/molmed.2015.00193

Table 2.

Comparison of murine and human fresh versus cryopreserved M(IL-4) by real-time PCR.

Fold-change over M(−)

Species Gene Fresh M(IL-4) Cryopreserved M(IL-4)
Mouse Arg1 183,966 ± 54,719a,b 1,254 ± 552
Nos2 11.06 ± 3.05a,b 2.31 ± 0.825
Chi3l3 (Ym1) 2,296 ± 678a,b 177 ± 17
Retnla (Relm-α) 1,955,323 ± 470,371a,b 72,331 ± 20,697
Human CD14 0.110 ± 0.0367a,b 0.0231 ± 0.0135a
MRC1 10.66 ± 1.64a,b 5.49 ± 1.41a
CCL18 64.75 ± 27.91a,b 4.27 ± 1.72

Mouse bone marrow–derived macrophages were treated with IL-4 for 48 h and compared before and after cryopreservation for AAM marker expression (Arg1, Chi3l3, Retnla) and Nos2 as a negative control. Likewise, fresh and frozen human monocyte–derived M(IL-4)s from healthy blood donors were compared on their capacity to downregulate CD14 and upregulate MRC1 and CCL18 transcripts. M(−), undifferentiated macrophage. Mouse, n = 7; human, n = 9. p < 0.05:

a

compared with M(−);

b

compared with cryopreserved M(IL-4).