Interaction between Ras and Bcl2L12 in B cells suppresses IL-10 expression

Clin Immunol. 2021 Aug:229:108775. doi: 10.1016/j.clim.2021.108775. Epub 2021 Jun 8.

Abstract

The pathogenesis of recurrent tonsillitis is to be further investigated. B cell-derived interleukin (IL)-10 plays a critical role in immune regulation. Ras activation plays an important role in cancer and many immune disorders. This study aims to investigate the role of Ras activation in down regulating IL-10 expression in tonsillar B cells. Surgically removed tonsil tissues were collected from patients with recurrent acute tonsillar inflammation; B cells were isolated from the tonsillar tissues by flow cytometry sorting to be analyzed by the Ras-specific enzyme-linked immunosorbent assay and pertinent immunological approaches. We found that, compared to peripheral B cells (pBC), B cells isolated from the tonsillar tissues with recurrent inflammation (tBC) showed higher Ras activation, lower IL-10 expression and higher Bcl2L12 expression. Bcl2L12 formed a complex with GAP (GTPase activating protein) to prevent Ras from deactivating. The Ras activation triggered the MAPK/Sp1 pathway to promote the Bcl2L12 expression in B cells. Bcl2L12 prevented the IL-10 expression in tBCs, that was counteracted by inhibition of Ras or the Ras signal transduction pathway. In conclusion, Bcl2L12 interacts with Ras activation to compromise immune tolerance in the tonsils by inhibiting the IL-10 expression in tBCs. Inhibition of Bcl2L12 can restore the IL-10 expression in tBCs.

Keywords: B cell; IL-10; Inflammation; Ras; Tonsil.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism*
  • B-Lymphocytes / pathology
  • Child
  • Down-Regulation
  • Female
  • GTPase-Activating Proteins / metabolism
  • Gene Knockdown Techniques
  • Humans
  • Immune Tolerance
  • Interleukin-10 / genetics
  • Interleukin-10 / metabolism*
  • Male
  • Muscle Proteins / antagonists & inhibitors
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2 / antagonists & inhibitors
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Recurrence
  • Rho Guanine Nucleotide Exchange Factors / genetics
  • Rho Guanine Nucleotide Exchange Factors / metabolism
  • Signal Transduction
  • Sp1 Transcription Factor / antagonists & inhibitors
  • Sp1 Transcription Factor / genetics
  • Sp1 Transcription Factor / metabolism
  • Tonsillitis / immunology
  • Tonsillitis / metabolism
  • Tonsillitis / pathology
  • Up-Regulation
  • Young Adult
  • ras Proteins / metabolism*

Substances

  • ARHGEF6 protein, human
  • BCL2L12 protein, human
  • GTPase-Activating Proteins
  • IL10 protein, human
  • Muscle Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Rho Guanine Nucleotide Exchange Factors
  • Sp1 Transcription Factor
  • SP1 protein, human
  • Interleukin-10
  • ras Proteins