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Updated: Feb 15, 2026

Bone Marrow-derived Macrophage Production
Published on: November 22, 2013
[Caspase-1 inhibitor AC-YVAD-CMK blocks IL-1β secretion of bone marrow-derived macrophages induced by Acinetobacter
Yimin Zhang1, Xuening Zhou2, Hongfang Zhang3
1Department of Pathogenic Biology and Examination, Shaanxi University of Chinese Medicine, Xianyang 712046, China. *Corresponding author,
Abstract:
Objective To explore the effect of caspase-1 selective inhibitor AC-YVAD-CMK on IL-1β secretion of bone marrow-derived macrophages (BMDMs) induced by Acinetobacter baumannii (A. baumannii). Methods Macrophages were separated from C57BL/6 mice which were stimulated using different concentrations of A. baumannii. The level of IL-1β in the culture supernatant was detected by ELISA. The expression of pro-IL-1β mRNA and protein were detected using the real-time quantitative PCR and Western blot analysis, respectively. The role of caspase-1 in the secretion of IL-1β was tested by AC-YVAD-CMK treatment to block caspase-1. Pneumonia models in C57BL/6 mice were prepared by A. baumannii inoculation. The level of IL-1β in bronchoalveolar lavage fluid (BALF) and the morphology of lung were detected by ELISA or HE staining, respectively. Results IL-1β level in the culture supernatant was up-reregulated by A. baumannii stimulation in a dose-dependent manner. The expression of pro-IL-1β mRNA and protein were not significantly changed with A. baumannii stimulation. Mature IL-1β secretion was blocked by AC-YVAD-CMK either in vitro or in vivo. The damage of lung induced by A. baumannii infection in mice was ameliorated by AC-YVAD-CMK. Conclusion AC-YVAD-CMK alleviates pulmonary pathological damage by reducing the caspase-1-mediated IL-1β secretion.
Insights
The caspase-1 inhibitor AC-YVAD-CMK reduces Interleukin-1 beta (IL-1β) secretion from macrophages stimulated by Acinetobacter baumannii. This inhibition alleviates lung damage in a mouse pneumonia model.
Area of Science:
- Immunology
- Microbiology
- Pathology
Background:
- Acinetobacter baumannii (A. baumannii) infection triggers inflammatory responses, including the secretion of Interleukin-1 beta (IL-1β).
- Caspase-1 plays a critical role in the maturation and release of IL-1β, a key cytokine in inflammation.
Purpose of the Study:
- To investigate the effect of the caspase-1 selective inhibitor AC-YVAD-CMK on IL-1β secretion induced by A. baumannii.
- To evaluate the therapeutic potential of AC-YVAD-CMK in an A. baumannii-induced pneumonia model.
Main Methods:
- Bone marrow-derived macrophages (BMDMs) were stimulated with A. baumannii, and IL-1β levels in supernatant were measured by ELISA.
- Pro-IL-1β mRNA and protein expression were assessed using real-time quantitative PCR and Western blot.
- Caspase-1 activity was inhibited using AC-YVAD-CMK in vitro and in vivo models.
- Pulmonary pathology was evaluated in mice infected with A. baumannii and treated with AC-YVAD-CMK.
Main Results:
- A. baumannii stimulation dose-dependently increased IL-1β levels in macrophage culture supernatants.
- Pro-IL-1β mRNA and protein expression remained unchanged despite A. baumannii stimulation.
- AC-YVAD-CMK effectively blocked mature IL-1β secretion both in vitro and in vivo.
- AC-YVAD-CMK treatment significantly ameliorated lung damage in mice infected with A. baumannii.
Conclusions:
- AC-YVAD-CMK effectively inhibits caspase-1-mediated IL-1β secretion induced by A. baumannii.
- Targeting caspase-1 with AC-YVAD-CMK demonstrates therapeutic potential for mitigating A. baumannii-induced pulmonary inflammation and damage.
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