CD47-dependent immunomodulatory and angiogenic activities of extracellular vesicles produced by T cells

Matrix Biol. 2014 Jul:37:49-59. doi: 10.1016/j.matbio.2014.05.007. Epub 2014 Jun 2.

Abstract

Intercellular communication is critical for integrating complex signals in multicellular eukaryotes. Vascular endothelial cells and T lymphocytes closely interact during the recirculation and trans-endothelial migration of T cells. In addition to direct cell-cell contact, we show that T cell derived extracellular vesicles can interact with endothelial cells and modulate their cellular functions. Thrombospondin-1 and its receptor CD47 are expressed on exosomes/ectosomes derived from T cells, and these extracellular vesicles are internalized and modulate signaling in both T cells and endothelial cells. Extracellular vesicles released from cells expressing or lacking CD47 differentially regulate activation of T cells induced by engaging the T cell receptor. Similarly, T cell-derived extracellular vesicles modulate endothelial cell responses to vascular endothelial growth factor and tube formation in a CD47-dependent manner. Uptake of T cell derived extracellular vesicles by recipient endothelial cells globally alters gene expression in a CD47-dependent manner. CD47 also regulates the mRNA content of extracellular vesicles in a manner consistent with some of the resulting alterations in target endothelial cell gene expression. Therefore, the thrombospondin-1 receptor CD47 directly or indirectly regulates intercellular communication mediated by the transfer of extracellular vesicles between vascular cells.

Keywords: CD47; Extracellular vesicles; Intercellular communication; Thrombospondin-1.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Angiogenesis Modulating Agents / metabolism*
  • Biological Transport / physiology
  • Blotting, Western
  • CD47 Antigen / metabolism*
  • Cell Communication / physiology*
  • DNA Primers / genetics
  • Endothelial Cells / metabolism
  • Extracellular Matrix / metabolism*
  • Flow Cytometry
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Immunologic Factors / physiology*
  • Immunoprecipitation
  • Jurkat Cells
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Thrombospondin 1 / metabolism
  • Transport Vesicles / metabolism*

Substances

  • Angiogenesis Modulating Agents
  • CD47 Antigen
  • CD47 protein, human
  • DNA Primers
  • Immunologic Factors
  • Thrombospondin 1
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