Studies on normal human bone marrow cultures in controlled environment thin-film culture systems
- PMID: 7532
- DOI: 10.1007/BF02796314
Studies on normal human bone marrow cultures in controlled environment thin-film culture systems
Abstract
Two thin film culture systems, the controlled environment steady state system (SS) and the rocker tube configuration of that system (RT), were used to identify some of the conditions that appear to maintain morphologic and functional characteristics of cells of human bone marrow explants in vitro. The systems configuration assured continual gassing, control and easy monitoring of the cultures. Cytocentrifuge preparations of media of specimens cultured in RT disclosed, though in decreasing numbers, various hematopoietic cells for periods exceeding one month. Hematopoietic cells shed from specimens cultured in the SS system were retained in the culture tubes; cells of the myelocytic series predominated for the first two weeks while an increasing number of monocytes and macrophages appeared in the media of of older cultures. Histologic examination of cultured explants disclosed preservation of the marrow architecture and the persistence of hematopoietic cells. Specimens cultured in RT tubes tended to be less cellular than similar cultures placed in dialysis bags or as cultured in the SS system. Immunoglobulins (Ig) were released into the culture media at a constant rate throughout the period of culture. Specimens that were cultured at a controlled pH of 7.4 released 2 to more than 4 times as much Ig as similar specimens maintained at a pH level of 7.1. There were no definitive differences in Ig levels in the cultures maintained at comparable pH levels and overlaid with various CO2 concentrations, i.e. 2%, 5%, 10% similarly, no differences in Ig levels were found in specimens cultured in media containing fetal bovine sera as opposed to horse sera.
Similar articles
-
Controlled environment culture of bone marrow explants from human myeloma.Cancer Res. 1976 Apr;36(4):1299-304. Cancer Res. 1976. PMID: 4220
-
Immunoglobulin heavy chain gene diversification in the long-term bone marrow culture of normal mice and mice with severe combined immunodeficiency.Eur J Immunol. 1987 Jul;17(7):1051-7. doi: 10.1002/eji.1830170723. Eur J Immunol. 1987. PMID: 3111857
-
Long-term cultures of murine fetal liver retain very early B lymphoid phenotype.J Exp Med. 1984 Oct 1;160(4):1087-101. doi: 10.1084/jem.160.4.1087. J Exp Med. 1984. PMID: 6434687 Free PMC article.
-
Lymphocyte function in human bone marrow. III. Isotype commitment, metabolic and secretory characteristics of immunoglobulin producing cells.Cell Immunol. 1986 Mar;98(1):34-45. doi: 10.1016/0008-8749(86)90265-0. Cell Immunol. 1986. PMID: 3742617
-
Long-term culture of canine marrow: cytogenetic evaluation of purging of lymphoma and leukemia.Exp Hematol. 1990 Oct;18(9):995-1001. Exp Hematol. 1990. PMID: 2397754
Cited by
-
Regulation of B-lymphocyte clonal proliferation by stimulatory and inhibitory macrophage-derived factors.J Exp Med. 1977 Nov 1;146(5):1420-35. doi: 10.1084/jem.146.5.1420. J Exp Med. 1977. PMID: 303681 Free PMC article.
-
Prostaglandin E production by human blood monocytes and mouse peritoneal macrophages.J Exp Med. 1978 Mar 1;147(3):952-7. doi: 10.1084/jem.147.3.952. J Exp Med. 1978. PMID: 632752 Free PMC article.
-
Effect of CO2 on short-term human lymphocyte culture in vitro.In Vitro. 1977 Nov;13(11):806-7. doi: 10.1007/BF02627861. In Vitro. 1977. PMID: 590972