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Human Long-Term Bone Marrow Culture

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Animal Cell Culture

Part of the book series: Methods in Molecular Biology ((MIMB,volume 5))

Abstract

Major advances in our understanding of human hematopoiesis have come from the development of semisolid in vitro culture techniques for the detection of progenitor cells capable of colony formation (see Chapter 28, this volume). However, colony assays select for hematopoietic precursors committed to a specific lineage(s) and, therefore, are of limited value in the assessment of very early progenitor cells. Also, they do not provide a means of assessing the influence of microenvironmental cells deemed essential for maintaining hematopoiesis in vivo (1). Furthermore, for the assays to be valid, cells must be plated at a sufficiently low concentration to ensure clonality (a condition in which each colony has arisen from a single progenitor cell). Consequently, cell-cell interactions that may be important in exerting regulatory effects on hematopoiesis are likely to be minimal.

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References

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© 1990 The Humana Press Inc.

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Keating, A., Toor, P. (1990). Human Long-Term Bone Marrow Culture. In: Walker, J.M., Pollard, J.W., Walker, J.M. (eds) Animal Cell Culture. Methods in Molecular Biology, vol 5. Humana Press. https://doi.org/10.1385/0-89603-150-0:331

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  • DOI: https://doi.org/10.1385/0-89603-150-0:331

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-150-0

  • Online ISBN: 978-1-59259-492-4

  • eBook Packages: Springer Protocols

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