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a Stem Cell Biology, National Medical Center, Budapest, Hungary;
b Lymphocyte Signal Transduction Laboratory, Institute of Genetics, Biological Research Center of Hungarian Academy of Sciences, Szeged, Hungary;
c Polyclinic of Hospitaller Brothers of St. John of God, Budapest, Hungary
Key Words. Apoptosis • Cobblestone areaforming cells • Galectin-1 Hematopoietic stem and progenitor cells • Human • Mouse
Correspondence: Ferenc Uher, Ph.D., National Medical Center, Stem Cell Biology, Diószegi ut 64., Budapest, Hungary, H-1113. Telephone: 36-1-372-4334; Fax: 36-1-372-4352; e-mail: uher{at}ohvi.hu
Galectin-1 is a member of the family of ß-galactoside binding animal lectins, galectins. Its presence in the bone marrow has been detected; however, its role in the regulation of hematopoiesis is unknown. In the present study, we have evaluated the effect of recombinant human galectin-1 on the proliferation and survival of murine and human hematopoietic stem and progenitor cells. We show that low amount of galectin-1 (10 ng/ml) increases the formation of granulocyte-macrophage and erythroid colonies and the frequencies of day-7 cobblestone areaforming cells on a lactose-inhibitable fashion. In contrast, high amount of galectin-1 (10 µg/ml) dramatically reduces the growth of the committed blood-forming progenitor cells as well as the much younger, lineage-negative hematopoietic cells (day-28 to -35 cobblestone areaforming cells). This inhibition is not blocked by lactose and, therefore, is largely independent of the ß-galactosidebinding site of the lectin. Furthermore, assays to detect apoptosis render it likely that the high amount of galectin-1 acts as a classical proapoptotic factor for the premature hematopoietic cells.
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