P2X7 receptor antagonism prevents IL-1 release from salivary epithelial cells and reduces inflammation in a mouse model of autoimmune exocrinopathy

Mahmoud G. Khalafalla, Lucas T. Woods, Jean M. Camden, Aslam A. Khan, Kirsten Limesand, Michael J. Petris, Laurie Erb, Gary A. Weisman

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Salivary gland inflammation is a hallmark of Sjögren’s syndrome (SS), a common autoimmune disease characterized by lymphocytic infiltration of the salivary gland and loss of saliva secretion, predominantly in women. The P2X7 receptor (P2X7R) is an ATP-gated nonselective cation channel that induces inflammatory responses in cells and tissues, including salivary gland epithelium. In immune cells, P2X7R activation induces the production of proinflammatory cytokines, including IL-1 and IL-18, by inducing the oligomerization of the multiprotein complex NLRP3-type inflammasome. Here, our results show that in primary mouse submandibular gland (SMG) epithelial cells, P2X7R activation also induces the assembly of the NLRP3 inflammasome and the maturation and release of IL-1, a response that is absent in SMG cells isolated from mice deficient in P2X7Rs (P2X7R/). P2X7R-mediated IL-1 release in SMG epithelial cells is dependent on transmembrane Na and/or K flux and the activation of heat shock protein 90 (HSP90), a protein required for the activation and stabilization of the NLRP3 inflammasome. Also, using the reactive oxygen species (ROS) scavengers N-acetyl cysteine and Mito-TEMPO, we determined that mitochondrial reactive oxygen species are required for P2X7R-mediated IL-1 release. Lastly, in vivo administration of the P2X7R antagonist A438079 in the CD28/, IFN/, NOD.H-2h4 mouse model of salivary gland exocrinopathy ameliorated salivary gland inflammation and enhanced carbachol-induced saliva secretion. These findings demonstrate that P2X7R antagonism in vivo represents a promising therapeutic strategy to limit salivary gland inflammation and improve secretory function.

Original languageEnglish (US)
Pages (from-to)16626-16637
Number of pages12
JournalJournal of Biological Chemistry
Volume292
Issue number40
DOIs
StatePublished - 2017

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Purinergic P2X7 Receptors
Interleukin-1
Epithelial Cells
Inflammation
Sialadenitis
Inflammasomes
Submandibular Gland
Salivary Glands
Chemical activation
Saliva
Reactive Oxygen Species
Acetylcysteine
HSP90 Heat-Shock Proteins
Multiprotein Complexes
Oligomerization
Interleukin-18
Carbachol
Infiltration
Autoimmune Diseases
Cysteine

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

P2X7 receptor antagonism prevents IL-1 release from salivary epithelial cells and reduces inflammation in a mouse model of autoimmune exocrinopathy. / Khalafalla, Mahmoud G.; Woods, Lucas T.; Camden, Jean M.; Khan, Aslam A.; Limesand, Kirsten; Petris, Michael J.; Erb, Laurie; Weisman, Gary A.

In: Journal of Biological Chemistry, Vol. 292, No. 40, 2017, p. 16626-16637.

Research output: Contribution to journalArticle

Khalafalla, Mahmoud G. ; Woods, Lucas T. ; Camden, Jean M. ; Khan, Aslam A. ; Limesand, Kirsten ; Petris, Michael J. ; Erb, Laurie ; Weisman, Gary A. / P2X7 receptor antagonism prevents IL-1 release from salivary epithelial cells and reduces inflammation in a mouse model of autoimmune exocrinopathy. In: Journal of Biological Chemistry. 2017 ; Vol. 292, No. 40. pp. 16626-16637.
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AU - Limesand, Kirsten

AU - Petris, Michael J.

AU - Erb, Laurie

AU - Weisman, Gary A.

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