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. 2019 Feb 27;316(5):R525–R534. doi: 10.1152/ajpregu.00019.2019

Fig. 8.

Fig. 8.

Effects of poly(inosinic:cytidylic) acid [poly(I:C)] administration on inflammatory gene expression in C-C chemokine receptor type 5 (CCR5)-deficient (CCR5−/−) and CCR5+/+ mice. A–G: macrophages, harvested from CCR5+/+ and CCR5−/− mice 6 h after intraperitoneal administration of poly(I:C) (100 µg/mouse) or saline, were lysed, and total RNA was isolated for determination of inflammatory (A–E) and type I IFN mRNA (F and G) gene accumulation by real-time PCR. COX-2, cyclooxygenase 2; iNOS, nitric oxide synthase. Results are means ± SE of 2–4 individual mice per condition. *P < 0.05.