The low cycling status of mobilized peripheral blood CD34+ cells is not restricted to the more primitive subfraction

Mobilized peripheral blood progenitor cells (PBPC) have been shown to differ qualitatively from bone marrow (BM) progenitors. The released progenitor cells are predominantly in G0/G1 and show a relatively high percentage of rhodamine dull cells. Within the BM these last two features are characterist...

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Veröffentlicht in:Leukemia 1998-04, Vol.12 (4), p.571-577
Hauptverfasser: Croockewit, A J, Raymakers, R A, Smeets, M E, vd Bosch, G, Pennings, A H, de Witte, T J
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container_end_page 577
container_issue 4
container_start_page 571
container_title Leukemia
container_volume 12
creator Croockewit, A J
Raymakers, R A
Smeets, M E
vd Bosch, G
Pennings, A H
de Witte, T J
description Mobilized peripheral blood progenitor cells (PBPC) have been shown to differ qualitatively from bone marrow (BM) progenitors. The released progenitor cells are predominantly in G0/G1 and show a relatively high percentage of rhodamine dull cells. Within the BM these last two features are characteristic of the more primitive progenitors. Although the mobilized PB cells can give rise to long-term repopulation and thus contain stem cells, the frequency of stem cells is not much higher if long-term initiating cell (LTC-IC) assays are used. To determine whether quiescent stem cells are selectively released or the low-cycle status of PB progenitors is related to the release from the BM microenvironment, the cell cycle status and rhodamine content in the PB and BM during mobilization were studied and compared with steady-state BM. More differentiated and more primitive progenitors were separated based on differentiation markers and cloned in single cell assay. In mobilized PB 54% of the CD34+ cells (n=5) were rhodamine dull compared to 22% in steady-state BM (P=0.014) [n=6]. The percentage of CD34+ cells in the S/G2M phases of the cell cycle was 2.1% in the mobilized PB (n=11), and 18% in steady-state BM (n=11) [P=0.002]. During mobilization the fraction of cells in the S/G2M phase of the cell cycle was 16% in BM (n=7), similar to steady-state BM (P=0.34). The released progenitors represented a selection of BM progenitors, with significantly more primitive progenitors (CD34+/13+/33dim) and less lymphoid precursors (CD34+/19+). Within the more differentiated CD34+113+/33bright, myelomonocytic precursors, both in PB as well as in BM, the percentage S/G2M was relatively higher than in the CD34+/13+/33dim subfraction: in normal BM: median 18% vs 8% (P=0.006) [n=8]; in mobilized PB 3% vs 2% (P=0.03) [n=10]; and in BM during mobilization 24% vs 7% (P=0.01) [n=6]. The cycle status of mobilized PB progenitors was low both in the primitive and more differentiated subfractions. During the mobilization period the BM progenitors are cycling as in steady-state BM. The low-cycle status of the mobilized PB progenitors may be related to the loss of contact with the micro-environment.
doi_str_mv 10.1038/sj.leu.2400981
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The released progenitor cells are predominantly in G0/G1 and show a relatively high percentage of rhodamine dull cells. Within the BM these last two features are characteristic of the more primitive progenitors. Although the mobilized PB cells can give rise to long-term repopulation and thus contain stem cells, the frequency of stem cells is not much higher if long-term initiating cell (LTC-IC) assays are used. To determine whether quiescent stem cells are selectively released or the low-cycle status of PB progenitors is related to the release from the BM microenvironment, the cell cycle status and rhodamine content in the PB and BM during mobilization were studied and compared with steady-state BM. More differentiated and more primitive progenitors were separated based on differentiation markers and cloned in single cell assay. In mobilized PB 54% of the CD34+ cells (n=5) were rhodamine dull compared to 22% in steady-state BM (P=0.014) [n=6]. 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The low-cycle status of the mobilized PB progenitors may be related to the loss of contact with the micro-environment.</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>9557616</pmid><doi>10.1038/sj.leu.2400981</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Antigens, CD34 - blood
Antigens, CD34 - physiology
Blood
Bone marrow
Bone Marrow Cells - cytology
Bone Marrow Cells - metabolism
CD34 antigen
Cell cycle
Cell Cycle - physiology
Cell Differentiation - physiology
Cell Division - physiology
Cell Fractionation
Cell Movement - physiology
Cycles
Flow Cytometry
Fluorescent Dyes - pharmacokinetics
G1 Phase - physiology
Hematopoietic Stem Cells - cytology
Hematopoietic Stem Cells - metabolism
Hemopoiesis
Humans
Immunophenotyping
Indicators and Reagents
Microenvironments
Osteoprogenitor cells
Peripheral blood
Precursors
Progenitor cells
Propidium
Repopulation
Resting Phase, Cell Cycle - physiology
Rhodamine
Rhodamine 123
Rhodamines - pharmacokinetics
S Phase - physiology
Staining and Labeling - methods
Steady state
Stem cells
title The low cycling status of mobilized peripheral blood CD34+ cells is not restricted to the more primitive subfraction
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