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Low‐oxygen and high‐carbon‐dioxide atmosphere improves the conservation of hematopoietic progenitors in hypothermia
Author(s) -
Jeanne Michel,
KovacevicFilipovic Milica,
Szyporta Milène,
Vlaski Marija,
Hermitte Francis,
Lafarge Xavier,
Duchez Pascale,
Boiron JeanMichel,
Praloran Vincent,
Ivanovic Zoran
Publication year - 2009
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/j.1537-2995.2009.02191.x
Subject(s) - haematopoiesis , progenitor cell , bone marrow , chemistry , stem cell , microbiology and biotechnology , andrology , apoptosis , cell cycle , biology , immunology , biochemistry , medicine
BACKGROUND: During short‐term storage of hematopoietic cells (HCs) at 4°C a substantial decline in number and in functional capacity of progenitors occurs after 3 days. We hypothesized that physiologic O 2 and CO 2 concentrations of hematopoietic tissue microenvironment (approx. 3% O 2 and approx. 6% CO 2 ) could improve cell viability and functionality during storage at 4°C. STUDY DESIGN AND METHODS: Mobilized peripheral blood (PB) CD34+ cells from multiple myeloma or non‐Hodgkin's lymphoma patients were stored in flasks containing air (approx. 20% O 2 and approx. 0.05% CO 2 ) or 3% O 2 /6% CO 2 atmosphere, for 3, 5, and 7 days at 4°C. The total number of cells, the number of cells in G0 or G1 phase of cell cycle, and the apoptosis rate were determined. The functional capacity of stored cells was assessed by the capacity of progenitors to form colonies in methylcellulose (colony‐forming cells [CFCs]) and of stem cells to repopulate the bone marrow (BM) of immunodeficient mice (SCID‐repopulating cell [SRC] assay). RESULTS: The total number of viable cells and cells in G1 phase as well as the number of total CFCs were significantly higher at 3% O 2 /6% CO 2 than in air at all time points. Cells in G0 phase and SRC were equally preserved in both conditions. CONCLUSION: Atmosphere with low O 2 and high CO 2 concentration (3% O 2 /6% CO 2 ) in hypothermia (+4°C) during 7 days of storage prevents cell damage and preserves a high number of functional HSCs and progenitors mobilized in PB by granulocyte–colony‐stimulating factor.