Augmentation of erythroid burst formation by the addition of thymocytes and other myelo-lymphoid cells
Autor: | John J. Trentin, Sandra C. Miller, Akihisa Kanamaru, M. T. Gallagher, Elisa M. Durban |
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Rok vydání: | 1980 |
Předmět: |
Physiology
T-Lymphocytes Clinical Biochemistry Bone Marrow Cells Spleen Thymus Gland Biology Mice medicine Animals Erythropoiesis Lymphocytes Progenitor cell Erythropoietin Incubation Lymph node Cells Cultured Specific-pathogen-free Pokeweed mitogen Cell Biology Molecular biology In vitro Specific Pathogen-Free Organisms Cortisone Mice Inbred C57BL medicine.anatomical_structure Immunology Mice Inbred CBA Bone marrow |
Zdroj: | Journal of Cellular Physiology. 104:187-197 |
ISSN: | 1097-4652 0021-9541 |
DOI: | 10.1002/jcp.1041040208 |
Popis: | Bone marrow from barrier-sustained specific pathogen-free (SPF) CBA and C57BL/6 mice gave relatively low numbers of BFU-E colonies in methylcellulose culture, as compared to conventional mice. Addition of thymocytes to the marrow cultures increased the yield of BFU-E colonies more than fourfold in SPF mice but only 1.5-fold in conventional mice. Colony size was also increased. Increased yield of BFU-E colonies was also obtained by co-culture of bone marrow with lymph node cells or with bone marrow or spleen cells from 900R whole-body irradiated mice. The effect appeared to be cellular rather than humoral. It was not reproduced by conditioned medium from thymus or pokeweed mitogen stimulated spleen cells. The helper effect of thymus cells was eliminated or reduced by freezing and thawing, or by 48 hours of incubation after irradiation. Treatment of bone marrow cells in vitro with anti-theta serum and complement did not decrease the number of BFU-E colonies. The putative helper cells appear not to be T cells, were non-adherent to the plastic culture dish, and were cortisone resistant and radioresistant. The low BFU-E colony yield from SPF mouse marrow is presumed to be largely the result of deficiency of these non-T helper cells in SPF bone marrow, rather than of BFU-E progenitor cells. |
Databáze: | OpenAIRE |
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