Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 5 | Cellular & Molecular Biology Letters

Fig. 5

From: Activation of BZW1 by CEBPB in macrophages promotes eIF2α phosphorylation-mediated metabolic reprogramming and endoplasmic reticulum stress in MRL/lpr lupus-prone mice

Fig. 5

Transcriptional activation of BZW1 by CEBPB promotes metabolic reprogramming of macrophages. BMDM were induced with Ova-IC and further treated with sh-NC or sh-CEBPB. A ECAR and OCR traces for BMDM. B The ECAR/OCR ratio in BMDM. C The glucose uptake capacity of BMDM was measured using a glucose uptake assay. D Glycolysis-related protein HK2 and LDHA expression in BMDM were measured using western blot assays. BMDM induced with Ova-IC were further treated with sh-CEBPB + oe-NC or sh-CEBPB + oe-BZW1. E BZW1 expression in BMDM after co-transfection. F ECAR and OCR traces for BMDM. G The ECAR/OCR ratio in BMDM. H The glucose uptake capacity of BMDM was measured using a glucose uptake assay. I Glycolysis-related protein HK2 and LDHA expression in BMDM were measured using western blot. J Expression of IL-1β, IL-6, and TNF-α in BMDM by RT–qPCR. K Expression of IL-1β, IL-6, and TNF-α in BMDM in response to 2DG by RT–qPCR. Data are presented as means ± SD and representative of three independent experiments (*p < 0.05). Data were statistically analyzed using an unpaired t-test (E, G, H), one-way ANOVA (B, C), or two-way ANOVA (A, D, F, IK)

Back to article page