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.
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Authors | O 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 |
Journal | Bulletin of experimental biology and medicine
(Bull Exp Biol Med)
Vol. 146
Issue 1
Pg. 96-9
(Jul 2008)
ISSN: 0007-4888 [Print] United States |
PMID | 19145362
(Publication Type: Journal Article)
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Chemical References |
- Antigens, CD34
- Peptides
- thymodepressin
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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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