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Fig. 4 | Arthritis Research & Therapy

Fig. 4

From: Dysregulated heme oxygenase-1low M2-like macrophages augment lupus nephritis via Bach1 induced by type I interferons

Fig. 4

Characteristics of cells within the glomeruli of BTB and CNC homology 1 (Bach1)-deficient MRL/lpr mice. Immunohistochemical staining of the renal tissues for CD68 (a, f), CD163 (b, g), heme oxygenase (HO)-1 (c, h), phosphorylated signal transducer and activator of transcription 1 (pSTAT1) (d, i), and CMAF (e, j) (original magnification × 400). k Numbers of CD68+, CD163+, and HO-1+ cells in glomeruli of mice. l Ratio of CD163+ and CD68+ cells within the glomerulus of Bach1+/+ and Bach1−/− MRL/lpr mice. m and n Numbers of pSTAT1+ and CMAF+ cells in glomeruli of Bach1+/+ and Bach1−/− MRL/lpr mice (n = 2 from each group). o Numbers of estimated M1 macrophage (Mϕ), M2 Mϕ, and HO-1+ cells in glomeruli in the renal tissues from Bach1+/+ and Bach1−/− MRL/lpr mice. Data shown are mean ± SEM. Three glomeruli from each mouse were evaluated. (p) CD163, (q) HO-1, and (r) interferon (IFN)-α messenger RNA (mRNA) from the whole kidneys. mRNA expression of (s) CD163 and (t) HO-1 of CD11b+ peritoneal Mϕ. *p < 0.05, **p < 0.01, ***p < 0.001 by Student’s t test. Data shown are mean ± SEM

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