Proteomic profiling of secreted proteins for the hematopoietic support of interleukin-stimulated human umbilical vein endothelial cells

Cell Transplant. 2013;22(7):1185-99. doi: 10.3727/096368912X657288. Epub 2012 Oct 1.

Abstract

Human umbilical cord vein endothelial cells (HUVECs) secrete a number of factors that greatly impact the proliferation and differentiation of hematopoietic stem and progenitor cells (HSPCs). These factors remain largely unknown. Here, we report on the most comprehensive proteomic profiling of the HUVEC secretome and identified 827 different secreted proteins. Two hundred and thirty-one proteins were found in all conditions, whereas 369 proteins were identified only under proinflammatory conditions following IL-1β, IL-3, and IL-6 stimulation. Thirteen proteins including complement factor b (CFb) were identified only under IL-1β and IL-3 conditions and may potentially represent HSPC proliferation factors. The combination of bioinformatics and gene ontology annotations indicates the role of the complement system and its activation. Furthermore, CFb was found to be transcriptionally strongly upregulated. Addition of complement component 5b-9 (C5b-9) monoclonal antibody to the stem cell expansion assay was capable of significantly reducing their proliferation. This study suggests a complement-mediated cross-talk between endothelial cells and HSPCs under proinflammatory conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antigens, CD34 / metabolism
  • Cell Proliferation / drug effects
  • Complement C5b / immunology
  • Complement System Proteins / metabolism
  • Computational Biology
  • Electrophoresis, Polyacrylamide Gel
  • Flow Cytometry
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects*
  • Hematopoietic Stem Cells / metabolism
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Interleukin-1beta / pharmacology*
  • Interleukin-3 / pharmacology*
  • Interleukin-6 / pharmacology*
  • Peptides / analysis
  • Proteomics*
  • Spectrometry, Mass, Electrospray Ionization
  • Up-Regulation

Substances

  • Antibodies, Monoclonal
  • Antigens, CD34
  • Interleukin-1beta
  • Interleukin-3
  • Interleukin-6
  • Peptides
  • Complement C5b
  • Complement System Proteins