ABSTRACT
We have investigated the expression of CD41a (gpIIbIIIa) on a subpopulation of human fetal bone marrow (FBM) CD34+ progenitor cells. Human FBM CD34+Lin- cells were subfractionated into CD41a+ and CD41a- subpopulations by flow cytometry. All the megakaryocyte colony-forming cells (CFU-MK) and almost all the burst-forming units-megakaryocyte (BFU-MK) were found within the CD41a+ subpopulation. In addition, a 14-fold greater number of granulocyte-macrophage colony-forming units (CFU-GM) and a five-fold greater number of mixed lineage progenitor cells (CFU-mix) were observed within the CD34+Lin-CD41a+ subpopulation compared to the CD34+Lin-CD41a- subpopulation. The high proliferative potential of CD34+Lin-CD41a+ cells was demonstrated by their capacity to expand in in vitro culture containing human plasma and recombinant Mpl ligand (thrombopoietin [Tpo]) with production of over 80% CD41b+ (gpIIb+) MKs. However, in long-term bone marrow cultures, the CD34+Lin-CD41a- population contained a significantly higher frequency of cobblestone area-forming cells (CAFC) than the CD34+Lin-CD41a+ population, indicating the presence of a primitive hematopoietic stem cell (HSC) population within the CD34+Lin-CD41a- subset. These data suggest that fetal CD34+Lin-CD41a+ cells are enriched for MK progenitor cells (CFU-MK and BFU-MK), myeloid progenitors, and CFU-mix but do not contain the more primitive CAFC.
Subject(s)
Antigens, CD34 , Bone Marrow/embryology , Platelet Glycoprotein GPIIb-IIIa Complex , Stem Cells/classification , Antigens, CD34/analysis , Bone Marrow Cells , Cell Differentiation , Cell Lineage , Cell Separation , Cells, Cultured , Colony-Forming Units Assay , Flow Cytometry , Hematopoietic Stem Cells/cytology , Humans , Immunophenotyping , Megakaryocytes/cytology , Platelet Glycoprotein GPIIb-IIIa Complex/analysis , Stem Cells/cytology , Thrombopoietin/analysisABSTRACT
Paris formosana Hayata (Liliaceae) grown in the mountain areas of Taiwan, has been used as a folk remedy for snake bite, and as an anti-inflammatory or anti-neoplastic agent. The effects of formosanin-C, a diosgenin saponin isolated from Paris formosana, on immune responses and transplantable murine tumor were studied. In culture systems, formosanin-C (0.03-0.16 microM) displayed significant enhancement of the blastogenic response of human peripheral blood cells to phytohemagglutinin. Formosanin-C also significantly increased the 3H-thymidine incorporation of ConA-stimulated lymphocytes at concentrations of 0.1 and 0.01 microM. The responsiveness of the granulocyte/macrophage colony-forming cells (GM-CFC) to mouse fibroblast cells L929 conditioned medium was altered in the presence of 0.01 and 0.001 microM of formosanin-C. In addition, formosanin-C given intraperitoneally activated natural killer cell activity at doses of 1-2.5 mg/kg. An intraperitoneal injection of 2.5 mg/kg of formosanin-C markedly induced interferon production, the peak blood level of which was observed 24 h after formosanin-C injection. Growth of subcutaneously transplanted MH134 mouse hepatoma was retarded by intraperitoneal treatment with 1-2.5 mg/kg of formosanin-C. The activity of 5-fluorouracil against MH-134 mouse hepatoma was potentiated by intraperitoneal treatment with formosanin-C. These results suggest that formosanin-C might display antitumor activity in association with modification of the immune system.
Subject(s)
Adjuvants, Immunologic , Antineoplastic Agents, Phytogenic , Diosgenin/analogs & derivatives , Saponins/pharmacology , Animals , Granulocyte-Macrophage Colony-Stimulating Factor/biosynthesis , Interferon Inducers , Killer Cells, Natural/drug effects , Liver Neoplasms, Experimental/drug therapy , Lymphocyte Activation/drug effects , Male , Mice , Mice, Inbred C3H , Plants, MedicinalABSTRACT
Heterocysts were able to be induced while the blue-green alga Anabaena HA 101 were grown in a medium free from ammonium nitrate, but the heterocyst formation was inhibited while the Anabaena were grown in medium containing 5 mM ammonium nitrate. Heterocysts which had already formed were enhanced to senescence by the ammonium nitrate. Heterocyst transformation from certain vegetative cells into adult heterocysts accompanied with protein synthesis. A maximal level of protein synthesis as well as the high activity of nitrogenase was detected while the late proheterocysts transformed to mature heterocysts. Heterocyst is the site of nitrogenase synthesis and of the nitrogen fixation.