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Human CD34+ HLA-DR- bone marrow cells contain progenitor cells capable of self-renewal, multilineage differentiation, and long-term in vitro hematopoiesis.
Srour, E F; Brandt, J E; Briddell, R A; Leemhuis, T; van Besien, K; Hoffman, R.
Afiliación
  • Srour EF; Department of Medicine, Indiana University School of Medicine, Indianapolis 46202-5121.
Blood Cells ; 17(2): 287-95, 1991.
Article en En | MEDLINE | ID: mdl-1717081
ABSTRACT
Human bone marrow cells expressing CD34 but not HLA-DR were isolated by immunofluorescence flow cytometric cell sorting. These cells contained a hematopoietic cell (CFU-B1) capable of producing, in an in vitro semisolid culture system, blast-cell-containing colonies, which possessed the capacity for self-renewal and commitment to multipotential differentiation. In addition, CD34+ HLA-DR- marrow cells contained primitive megakaryocyte progenitor cells, the burst-forming unit-megakaryocyte (BFU-MK). A subset of CD34+ HLA-DR- marrow cells lacking the expression of CD15 and CD71 was obtained by flow cytometric cell sorting and was capable of sustaining in vitro hematopoiesis in suspension culture for up to 8 weeks in the absence of a preestablished adherent marrow cell layer. The combination of IL-3 + IL-1 alpha and IL-3 + IL-6 sustained proliferation of these cells for 8 weeks, induced maximal cellular expansion, and increased the numbers of assayable progenitor cells. These studies demonstrate that human CD34+ HLA-DR- marrow cells and their subsets contain primitive multipotential hematopoietic cells capable of self-renewal and of differentiation into multiple hematopoietic lineages.
Asunto(s)
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Colección: 01-internacional Asunto principal: Médula Ósea / Células Madre Hematopoyéticas / Antígenos HLA-DR / Antígenos CD / Hematopoyesis Límite: Humans Idioma: En Revista: Blood Cells Año: 1991 Tipo del documento: Article
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Colección: 01-internacional Asunto principal: Médula Ósea / Células Madre Hematopoyéticas / Antígenos HLA-DR / Antígenos CD / Hematopoyesis Límite: Humans Idioma: En Revista: Blood Cells Año: 1991 Tipo del documento: Article