PCR array and protein array studies demonstrate that IL-1β (interleukin-1β) stimulates the expression and secretion of multiple cytokines and chemokines in human adipocytes

Alomar, Suliman Yousef and Zaibi, Mohamed S. and Kępczyńska, Malgorzata A. and Gentili, Alessandra and Alkhuriji, Afrah and Mansour, Lamjad and Ahmed Dar, Javid and Trayhurn, Paul (2015) PCR array and protein array studies demonstrate that IL-1β (interleukin-1β) stimulates the expression and secretion of multiple cytokines and chemokines in human adipocytes. Archives of Physiology and Biochemistry, 121 (5). pp. 187-193. ISSN 1381-3455 (Print), 1744-4160 (Online)

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Abstract

The role of IL-1β in regulating the expression and secretion of cytokines and chemokines by human adipocytes was examined. Adipocytes were incubated with human IL-1β for 4 or 24 h. The expression of a panel of 84 cytokine/chemokine genes was probed using PCR arrays. IL-1β stimulated the expression of >30 cytokine/chemokine genes on the arrays; 15 showed >100-fold increases in mRNA at 4 or 24 h including CSF3, CXCL1, CXCL2, CXCL12 and IL8. CSF3 exhibited a 10,000-fold increase in mRNA at 4 h. ADIPOQ was among the genes whose expression was inhibited. Protein arrays were used to examine the secretion of cytokines/chemokines from adipocytes. IL-1β stimulated the secretion of multiple cytokines/chemokines including MCP-1, IL-8, IP-10, MIP-1α and MCP-4. The most responsive was IP-10, which exhibited a 5,000-fold increase in secretion with IL-1β. IL-1β is likely to play a substantial role in stimulating the inflammatory response in human adipocytes in obesity.

Item Type: Article
Additional Information: Peer reviewed journal article; Final Accepted Version Deposited
Uncontrolled Keywords: Adipose tissue; Gene expression; Inflammation; Obesity
Subjects: Q Science > QP Physiology
R Medicine > RZ Other systems of medicine
Divisions: School of Science > Metabolic Research
Depositing User: Paul Trayhurn
Date Deposited: 14 Apr 2016 10:56
Last Modified: 03 Feb 2017 12:42
URI: http://bear.buckingham.ac.uk/id/eprint/112

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