Ex vivo expansion of cord blood-CD34(+) cells using IGFBP2 and Angptl-5 impairs short-term lymphoid repopulation in vivo

J Tissue Eng Regen Med. 2013 Dec;7(12):944-54. doi: 10.1002/term.1486. Epub 2012 Jun 1.

Abstract

Cord blood-derived haematopoietic stem cells (CB-HSCs) are an attractive source for transplantation in haematopoietic disorders. However, the yield of CB-HSCs per graft is limited and often insufficient, particularly for the treatment of adult patients. Here we compare the capacity of three cytokine cocktails to expand CB-CD34(+) cells. Cells were cultured for 5 or 14 days in media supplemented with: (a) SCF, FL, IL-3 and IL-6 (SFLIL3/6); (b) SCF, TPO, FGF-1 and IL-6 (STFIL6); and (c) SCF, TPO, FGF-1, IGFBP2 and Angptl-5 (STFAI). We observed that STFAI-culture expansion sustained the most vigorous cell proliferation, maintenance of CD34(+) phenotype and colony-forming unit counts. In addition, STFAI-cultured cells had a potent ex vivo migration activity. STFAI-expanded cells were able to engraft NSG mice. However, no significant difference in overall engraftment was observed among the expansion cocktails. Assessment of short-term reconstitution using multilineage markers demonstrated that the STFAI cocktail for HSCs expansion greatly improved total cell expansion but may impair short-term lymphoid repopulation.

Keywords: cytokines; expansion; haematopoietic stem cells; transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiopoietins / pharmacology*
  • Animals
  • Antigens, CD34 / metabolism*
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / drug effects
  • Cell Differentiation / drug effects
  • Cell Movement / drug effects
  • Cell Polarity / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Clone Cells
  • Colony-Forming Units Assay
  • Cytokines / pharmacology
  • Fetal Blood / cytology*
  • Fetal Blood / drug effects*
  • Fetal Blood / metabolism
  • Humans
  • Insulin-Like Growth Factor Binding Protein 2 / pharmacology*
  • Leukocyte Common Antigens / metabolism
  • Lymphocytes / cytology*
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Spleen / cytology
  • Stem Cell Factor / pharmacology
  • Thrombopoietin / pharmacology

Substances

  • Angiopoietins
  • Antigens, CD34
  • Cytokines
  • Insulin-Like Growth Factor Binding Protein 2
  • Stem Cell Factor
  • Thrombopoietin
  • Leukocyte Common Antigens