Overexpression of TGF-ß 1 gene induces cell surface localized glucose-regulated protein 78-associated latency-associated peptide/TGF-ß

J Immunol. 2010 Sep 15;185(6):3529-35. doi: 10.4049/jimmunol.0904121. Epub 2010 Aug 18.

Abstract

TGF-beta plays a crucial role in immune regulation. It has been reported that pro-TGF-beta, latency-associated peptide (LAP), latent TGF-beta and/or active TGF-beta (LAP/TGF-beta) is localized on the cell surface of Foxp3(+) regulatory T cells. However, the molecular mechanism(s) of how LAP/TGF-beta is anchored on the cell membrane is unknown. In this study, we show that forced expression of human TGF-beta(1) gene by retrovirus transduction into P3U1 mouse myeloma cells, and other cell types including murine CD4(+)CD25(-) T cells, makes these cells surface LAP/TGF-beta-positive. The surface LAP/TGF-beta contains high-glycosylated, furin-processed latent TGF-beta, which is different from the low-glycosylated, furin-unprocessed intracellular form or the high-glycosylated, furin-unprocessed secreted form. Furthermore, surface LAP/TGF-beta forms a complex with the molecular chaperone glucose-regulated protein 78 (GRP78, also known as BiP), and knockdown of GRP78 reduced the expression levels of surface LAP/TGF-beta. GRP78, however, is not involved in GARP-mediated surface LAP/TGF-beta. Our results suggest that GRP78 provides an additional surface localization mechanism for LAP/TGF-beta, which may play an important role in controlling TGF-beta activity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Line
  • Cell Line, Tumor
  • Cell Membrane / genetics
  • Cell Membrane / immunology*
  • Cell Membrane / metabolism
  • Endoplasmic Reticulum Chaperone BiP
  • Furin / metabolism
  • Gene Expression Regulation, Viral / immunology*
  • Glycosylation
  • Heat-Shock Proteins / biosynthesis*
  • Heat-Shock Proteins / metabolism
  • Humans
  • Intracellular Fluid / immunology
  • Intracellular Fluid / metabolism
  • Jurkat Cells
  • Lentivirus / genetics
  • Mice
  • Mice, Inbred BALB C
  • Peptides / metabolism
  • Protein Precursors / biosynthesis*
  • Protein Precursors / metabolism
  • Protein Processing, Post-Translational / immunology
  • Protein Sorting Signals
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism
  • Transduction, Genetic
  • Transforming Growth Factor beta / biosynthesis*
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta1 / biosynthesis*
  • Transforming Growth Factor beta1 / genetics*
  • Transforming Growth Factor beta1 / physiology

Substances

  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Hspa5 protein, mouse
  • Peptides
  • Protein Precursors
  • Protein Sorting Signals
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • latency-associated propeptide, TGF-beta
  • Furin