Co-culture system of human salivary gland epithelial cells and immune cells from primary Sjögren's syndrome patients: an in vitro approach to study the effects of Rituximab on the activation of the Raf-1/ERK1/2 pathway

Int Immunol. 2015 Apr;27(4):183-94. doi: 10.1093/intimm/dxu100. Epub 2014 Nov 8.

Abstract

Primary Sjögren's syndrome (pSS) is a chronic autoimmune disorder of the exocrine glands with associated lymphocytic infiltrates in the affected glands. Dryness of the mouth and eyes results from involvement of the salivary and lacrimal glands. The efficacy of Rituximab (RTX) in pSS is still open to debate. This study delineates the signaling pathway involved in RTX-mediated down-regulation of pro-inflammatory factors in a co-culture system of pSS salivary gland epithelial cells (SGEC) with syngeneic pSS B-lymphocytes. In addition, the effects of RTX on the activation of the Raf-1/ERK1/2 pathway in pSS SGEC co-cultured with syngeneic pSS T-lymphocytes were also investigated. This study demonstrated that RTX may interfere with the ERK1/2 pathway in a syngeneic co-culture of pSS SGEC with pSS B-lymphocytes, leading to decreased cytokine production by SGEC. These novel findings reveal that syngeneic co-culture of pSS SGEC with pSS B-lymphocytes leads to a down-regulation of Raf-1 in epithelial cells that adversely regulates the activity of the ERK1/2 pathway and determines a subsequent reduction of the release of pro-inflammatory factors.

Keywords: ERK; Raf-1; Rituximab; Sjögren’s syndrome; cytokines.

MeSH terms

  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines / metabolism
  • Enzyme Activation / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Flavonoids / pharmacology
  • Humans
  • Inflammation / drug therapy
  • Inflammation / immunology
  • Inflammation Mediators / metabolism
  • MAP Kinase Signaling System / drug effects*
  • Mitogen-Activated Protein Kinase 1 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-raf / biosynthesis
  • Proto-Oncogene Proteins c-raf / metabolism*
  • RNA, Messenger / biosynthesis
  • Rituximab / pharmacology*
  • Salivary Glands / cytology
  • Salivary Glands / immunology*
  • Sjogren's Syndrome / drug therapy
  • Sjogren's Syndrome / pathology*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology

Substances

  • Cytokines
  • Flavonoids
  • Inflammation Mediators
  • Protein Kinase Inhibitors
  • RNA, Messenger
  • Rituximab
  • Proto-Oncogene Proteins c-raf
  • MAPK1 protein, human
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one