Brief Article
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World J Biol Chem. May 26, 2013; 4(2): 30-34
Published online May 26, 2013. doi: 10.4331/wjbc.v4.i2.30
Caspase-1 activation and mature interleukin-1β release are uncoupled events in monocytes
Amy J Galliher-Beckley, Li-Qiong Lan, Shelly Aono, Lei Wang, Jishu Shi
Amy J Galliher-Beckley, Li-Qiong Lan, Lei Wang, Jishu Shi, Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, United States
Li-Qiong Lan, College of Life Sciences, Sichuan University, Chengdu 610065, Sichuan Province, China
Shelly Aono, Department of Anatomy, Physiology, and Pharmacology, College of Veterinary Medicine, Auburn University, Auburn, AL 36849, United States
Author contributions: Galliher-Beckley AJ and Lan LQ contribute equally, Galliher-Beckley AJ conceived experiments, analyzed data, and wrote the manuscript; Aono S conceived and performed experiments, analyzed data, and helped write the manuscript; Lan LQ conceived and performed experiments, analyzed data; Wang L and Shi J conceived experiments, analyzed data, and wrote the manuscript.
Supported by NIH R21 AI085416 (to Shi J) and NIH NCRR P20-RR017686 (to PI: Daniel Marcus; Shi J)
Correspondence to: Dr. Jishu Shi, Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, 119 Anderson Hall, Manhattan, KS 66506, United States. jshi@ksu.edu
Telephone: +1-785-5324506 Fax: +1-785-5324557
Received: February 13, 2013
Revised: March 26, 2013
Accepted: April 10, 2013
Published online: May 26, 2013
Processing time: 86 Days and 13 Hours
Abstract

AIM: To investigate whether caspase-1 activation/intracellular processing of pro-interleukin-1β (pro-IL-1β) and extracellular release of mature IL-1β from activated monocytes are separable events.

METHODS: All experiments were performed on fresh or overnight cultured human peripheral blood monocytes (PBMCs) that were isolated from healthy donors. PBMCs were activated by lipopolysaccharide (LPS) stimulation before being treated with Adenosine triphosphate (ATP, 1 mmol/L), human α-defensin-5 (HD-5, 50 μg/mL), and/or nigericin (Nig, 30 μmol/L). For each experiment, the culture supernatants were collected separately from the cells. Cell lysates and supernatants were both subject to immunoprecipitation with anti-IL-1β antibodies followed by western blot analysis with anti-caspase-1 and anti-IL-1β antibodies.

RESULTS: We found that pro-IL-1β was processed to mature IL-1β in LPS-activated fresh and overnight cultured human monocytes in response to ATP stimulation. In the presence of HD-5, this release of IL-1β, but not the processing of pro-IL-1β to IL-1β, was completely inhibited. Similarly, in the presence of HD-5, the release of IL-1β, but not the processing of IL-1β, was significantly inhibited from LPS-activated monocytes stimulated with Nig. Finally, we treated LPS-activated monocytes with ATP and Nig and collected the supernatants. We found that both ATP and Nig stimulation could activate and release cleaved caspase-1 from the monocytes. Interestingly, and contrary to IL-1β processing and release, caspase-1 cleavage and release was not blocked by HD-5. All images are representative of three independent experiments.

CONCLUSION: These data suggest that caspase-1 activation/processing of pro-IL-1β by caspase-1 and the release of mature IL-1β from human monocytes are distinct and separable events.

Keywords: Caspase-1; Human defensin; Monocytes; Interleukin-1β processing and release; Inflammasome

Core tip: Activated macrophages release large amounts of interleukin-1β (IL-1β) and macrophages deficient in caspase-1 expression have undetectable IL-1β secretion. This suggests that IL-1β release and caspase-1 activation are closely related events. We found that human α-defensin 5 (HD-5) inhibited the release of IL-1β, but not the processing of pro-IL-1β to IL-1β in lipopolysaccharide-activated monocytes stimulated with Adenosine triphosphate or nigericin. Different from IL-1β processing and release, the activation and release of caspase-1 from stimulated monocytes was not blocked by HD-5. These data suggest that caspase-1 activation/processing of pro-IL-1β by caspase-1 and the release of mature IL-1β from human monocytes are distinct and separable events.