The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
The role of cells and their products in the regulation of in vitro stem cell proliferation and granulocyte development
Abstract
In long‐term marrow cultures haemopoiesis can be maintained in vitro for up to 6 months. Critical analysis of the cell populations produced has shown that the stem cells and their committed progeny have characteristics in common with the corresponding cell types in vivo. The maintenance of haemopoiesis in vitro is associated with the development of an appropriate inductive environment provided by bone marrow derived adherent cells. Analysis of the interactions between environmental and haemopoietic cells has been facilitated by the development of in vitro systems reproducing the naturally occurring genetic environmental defects and other systems where the development of a competent inductive environment shows a dependency upon corticosteroid hormones. Investigations have shown that stem cell proliferation may be controlled by production of opposing activities, one stimulatory for DNA synthesis, the other inhibitory. A model is proposed whereby modulation in the production of these factors is determined by the physical presence of stem cells in a proposed cellular milieu, within the adherent layer. The adherent layer, apart from acting at the level of stem cell proliferation, can also modify the response of differentiating cells (eg, GM‐CFC) to exogenous stimulatory activities. Addition of GM‐CSF or of CSF‐antiserum has no effect on haemopoiesis in long‐term cultures.
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“MSCs derived from bone marrow (BM)-MSCs being able to ensure the growth and viability of hematopoietic stem cells in co-culture conditions without growth factor supplementation [5], [6].”
From Mesenchymal stem cell secretome for regenerative medicine: Where do we stand? (2025) · cites this paper as [6]
Citations
Cites
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells1
Till, J. E., & McCulloch, E. A. (2011) · Radiation Research · doi:10.1667/rrxx28.1 · Cited by 4,036
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells
Till, J. E., & McCulloch, E. A. (1961) · Radiation Research · doi:10.2307/3570892 · Cited by 3,708
Conditions controlling the proliferation of haemopoietic stem cells in vitro
Dexter, T. M., Allen, T. D., & Lajtha, L. G. (1977) · Journal of Cellular Physiology · doi:10.1002/jcp.1040910303 · Cited by 2,066
Self-citationTHE GROWTH OF MOUSE BONE MARROW CELLS IN VITRO
Bradley, T., & Metcalf, D. (1966) · Australian Journal of Experimental Biology and Medical Science · doi:10.1038/icb.1966.28 · Cited by 1,926
Biology of the Laboratory Mouse
HESTON, W. E. (1967) · Journal of Heredity · doi:10.1093/oxfordjournals.jhered.a107528 · Cited by 1,394
The cloning of normal “Mast” cells in tissue culture
Pluznik, D. H., & Sachs, L. (1965) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030660309 · Cited by 872
Induction of Colonies of Hemoglobin-Synthesizing Cells by Erythropoietin In Vitro
Stephenson, J. R., Axelrad, A. A., McLeod, D. L., & Shreeve, M. M. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.7.1542 · Cited by 611
LAJTHA, L. G. (1979) · Differentiation · doi:10.1111/j.1432-0436.1979.tb01007.x · Cited by 552
Self-citationDifferentiation of normal and neoplastic hematopoietic cells
Clarkson, B. D., Marks, P. A., & Till, J. E. (1978) · Cold Spring Harbor Laboratory eBooks · Cited by 406
The induction of clones of normal mast cells by a substance from conditioned medium
Pluznik, D. H., & Sachs, L. (1966) · Experimental Cell Research · doi:10.1016/0014-4827(66)90026-7 · Cited by 354
Research works printed but not linked: 10
- Iscove NN, 1973, Haemopoiesis in Culture: Second International Workshop, 74
- Dexter TM, 1978, Cold Spring Harbor Symp Quant Biol, 42, 63
- Reimann J, 1979, Exp Hematol, 7, 45
- Dexter TM, 1979, Clinics in Hematology, 453
- Dexter TM, 1977, Biomedicine, 27, 344
- ToksözD DexterTM LordBI WrightEG LajthaLG:Blood(in press).
- Lord BI, 1977, Biomedicine, 27, 223
- Frindel E, 1976, Exp Hematol, 4, 56
- Frindel E, 1977, Exp Hematol, 5, 74
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Cited by
Mesenchymal stem cell secretome for regenerative medicine: Where do we stand?
Trigo, C. M., Rodrigues, J. S., Camões, S. P., Solá, S., & Miranda, J. P. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2024.05.004 · Cited by 252
“Therefore, a new perspective began to take shape with MSCs derived from bone marrow (BM)-MSCs being able to ensure the growth and viability of hematopoietic stem cells in co-culture conditions without growth factor supplementation [5,6].”
Metadata
- Authors
- Dexter, T. M., Spooncer, E., Toksoz, D., & Lajtha, L. G.
- Affiliations
- Cancer Research UK Manchester Institute (GB)
- Venue
- Journal of Supramolecular Structure
- Publisher
- Wiley
- Published
- 1980-01
- Volume
- 13
- Issue
- 4
- Pages
- 513-524
- ISSN
- 0091-7419 (ISSN-L)
- 1547-9366
- OpenAlex
- W1972839143
- Cited by
- 81
- References
- 38
- Citations by year
- 2025: 1 · 2024: 1 · 2021: 1 · 2019: 1 · 2016: 1 · 2014: 1 · 2012: 2
- FWCI
- 2.99
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Supramolecular Structure (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Health Sciences › Medicine › Hematology › Blood disorders and treatments
- Keywords
- hematopoiesis, long-term bone marrow culture, hematopoietic stem cells, stem cell proliferation, corticosteroids, granulocyte-macrophage colony-forming cells, GM-CSF, cell-cell interactions, DNA synthesis regulation
- MeSH terms
- Animals, Bone Marrow, Cell Adhesion, Cell Differentiation, Cell Division, Cells, Cultured, Granulocytes, Hematopoiesis, Hematopoietic Stem Cells, Kinetics, Methods, Mice, Mutant Strains, Mice
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.