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Dipeptide gamma-d-Glu-d-Trp (thymodepressin) inhibits migration of CD34+ cells from the bone marrow into peripheral blood during tumor growth.

Abstract
We studied the effect of dipeptide gamma-d-Glu-d-Trp (thymodepressin) on migration of CD34+ hemopoietic precursors and their direct adhesion to fibronectin in tumor-bearing mice on days 8, 11, 15, and 17 of tumor growth and on expression of CXCR-4 (CD184+) to SDF-1 and integrin beta1 (CD29+) by bone marrow cells. In tumor-bearing mice treated with gamma-d-Glu-d-Trp, the percent of CD34+ hemopoietic precursors in the peripheral blood considerably decreased throughout the observation period; the content of CD34+ hemopoietic precursors in the tumor tissue was 2-3-fold below the control against the background of increased content of CD34+ cells in the bone marrow. In animals treated with the peptide, the content of cells expressing CXCR-4 in the peripheral blood, bone marrow, and tumor tissue significantly decreased, while the percent of cells expressing integrin beta1 receptor (CD29+) in the bone marrow increased 2-fold, which was paralleled by an almost 2-fold increase in the percent of cells binding to fibronectin. We hypothesized that dipeptide gamma-d-Glu-d-Trp suppressed mobilization/migration of CD34+ hemopoietic precursor cells from the bone marrow to the peripheral blood of tumor-bearing mice.
AuthorsO V Semina, T N Semenets, I A Zamulaeva, E I Selivanova, T P Iljina, Ya V Maliutina, D Yu Semin, V I Deigin, A S Saenko
JournalBulletin of experimental biology and medicine (Bull Exp Biol Med) Vol. 146 Issue 1 Pg. 96-9 (Jul 2008) ISSN: 0007-4888 [Print] United States
PMID19145362 (Publication Type: Journal Article)
Chemical References
  • Antigens, CD34
  • Peptides
  • thymodepressin
Topics
  • Animals
  • Antigens, CD34 (metabolism)
  • Bone Marrow Cells (drug effects, physiology)
  • Cell Movement (drug effects, physiology)
  • Female
  • Hematopoietic Stem Cells (drug effects, physiology)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Neoplasms (pathology, physiopathology)
  • Peptides (pharmacology)

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