In spite of the apparent depletion of mast cells in tissues of mutant mice of W/W" genotype, cells with many features of mast cells do develop when bone marrow cells of W/W" mice are cultured in the presence of pokeweed mitogen-stimulated spleen cell-conditioned medium (PWM-SCM). In order to resolve
Proliferation and differentiation in culture of mast cell progenitors derived from mast cell-deficient mice of genotype W/Wv
β Scribed by Toshio Suda; Junko Suda; Samuel S. Spicer; Makio Ogawa
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 608 KB
- Volume
- 122
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Mice of genotype W/Wv have less than 1% of normal mast cells in the skin, stomach, and cecum. In order to further clarify the mechanism of this deficiency, we studied committed mast cell progenitors and multipotent progenitors, which are capable of mast cell differentiation in clonal culture. The relative concentration of mast cell progenitors in the bone marrow, spleen, and peripheral blood of W/Wv mice was similar to that of +/+ mice. However, the cellularity of the marrows of W/Wv mice was 54% of that of their normal littermates. Identification of mast cells was established by metachromatic staining with toluidine blue, transmission electron microscopy, and demonstration of membrane receptors for immunoglobulin E. The time course of colony formation and the morphology of W/Wv mast cell colonies in culture was identical to that of normal littermates. The percentages of mast cells in individual multi-lineage colonies were extremely variable. The histamine content of mast cells derived from W/Wv mice was similar to that of mast cells from +/+ mice. These studies demonstrated the normal capacity for differentiation and proliferation in culture of mast cell progenitors from W/Wv mice.
π SIMILAR VOLUMES
C57BL/6)F,-Sl/Sld (hereafter, WCB6F,-Sl/Sld) mice are sterile due to the deficient spermatogenesis in the testes. The cause of deficient spermatogenesis in WBB6FI-W/W mice is considered to be a defect in germ cells themselves, whereas that in WCB6FI-Sl/Sld mice is considered to be a defect in tissue
By using Dexter-type long-term marrow cultures (D-LTMC), it has been shown previously that hematopoietic progenitor cells (HPC) from patients with aplastic anemia (AA) have a deficient proliferation in vitro. The studies reported to date, however, have focused exclusively on granulomonocytic progeni