Literature DB >> 3872887

Identification of three accessory cell populations in human bone marrow with erythroid burst-promoting properties.

D C Linch, J M Lipton, D G Nathan.   

Abstract

Several laboratories have demonstrated a requirement for burst-promoting activity (BPA), a product of T cells, or T cell/monocyte collaboration in the induction of differentiation of peripheral blood erythroid burst-forming units (BFU-E) in vitro. The physiologic significance of this finding is brought into question by patients with severe mature T cell deficiency who have normal in vivo erythropoiesis. The studies described here were designed to determine whether the burst-promoting effects of marrow T cells and adherent cells are similar to those of peripheral blood, to define whether a third population of marrow cells is capable of production of BPA, and to describe the BPA requirements of immature and mature marrow erythroid progenitors. To that end we prepared adherence- and E-depleted low-density peripheral blood mononuclear cells as a source of BFU-E and demonstrated that their optimal erythropoietin-induced differentiation requires BPA. We then determined that both bone marrow and peripheral blood T cells and monocytes could provide the necessary BPA to induce their erythropoietin dependent differentiation. BPA production by T cells was sensitive to irradiation, but that of the whole bone marrow low-density population was considerably less sensitive. This in itself demonstrated that BPA production in marrow is not T cell dependent. We further demonstrated a potent, albeit infrequent, third population of BPA-producing marrow cells. These proved to be nonadherent, E receptor-negative, granulocyte antigen-negative, and gamma-Fc receptor-positive. Finally, we separated all of these BPA-producing cells from marrow erythroid progenitors and concentrated the latter into a population in which they comprised 6% of the cells. With this population we demonstrated that both immature (BFU-E) and mature (colony-forming units [CFU-E]) erythroid progenitors require BPA in addition to erythropoietin to induce them to form erythroid colonies in vitro. These results may explain the normal erythropoiesis found in patients with mature T cell deficiency. Though the differentiation of both BFU-E and CFU-E requires BPA, this need can be met by a special class of nonadherent, radioresistant, E receptor-negative, granulocyte antigen-negative, and gamma-Fc-positive cells.

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Year:  1985        PMID: 3872887      PMCID: PMC425456          DOI: 10.1172/JCI111827

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  28 in total

1.  Receptors for IgG molecules on human lymphocytes forming spontaneous rosettes with sheep red cells.

Authors:  M Ferrarini; L Moretta; R Abrile; M L Durante
Journal:  Eur J Immunol       Date:  1975-01       Impact factor: 5.532

2.  The role of erythropoietin in regulation of population size and cell cycling of early and late erythroid precursors in mouse bone marrow.

Authors:  N N Iscove
Journal:  Cell Tissue Kinet       Date:  1977-07

3.  An improved rosetting assay for detection of human T lymphocytes.

Authors:  M E Kaplan; C Clark
Journal:  J Immunol Methods       Date:  1974-07       Impact factor: 2.303

4.  Erythropietic colonies in cultures of human marrow.

Authors:  A D Tepperman; J E Curtis; E A McCulloch
Journal:  Blood       Date:  1974-11       Impact factor: 22.113

5.  Erythroid colony formation in cultures of mouse and human bone marrow: analysis of the requirement for erythropoietin by gel filtration and affinity chromatography on agarose-concanavalin A.

Authors:  N N Iscove; F Sieber; K H Winterhalter
Journal:  J Cell Physiol       Date:  1974-04       Impact factor: 6.384

6.  Cytochemical identification of monocytes and granulocytes.

Authors:  L T Yam; C Y Li; W H Crosby
Journal:  Am J Clin Pathol       Date:  1971-03       Impact factor: 2.493

7.  Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies.

Authors:  B J Clarke; D G Nathan; B P Alter; B G Forget; D G Hillman; D Housman
Journal:  Blood       Date:  1979-10       Impact factor: 22.113

8.  Human erythroid burst-promoting activity produced by phytohemagglutinin-stimulated, radioresistant peripheral blood mononuclear cells.

Authors:  D Meytes; J A Ma Ortega; N A Shore; P P Dukes
Journal:  Blood       Date:  1979-11       Impact factor: 22.113

9.  Erythropoietin (Ep) dose-response curves for three classes of erythroid progenitors in normal human marrow and in patients with polycythemia vera.

Authors:  C J Eaves; A C Eaves
Journal:  Blood       Date:  1978-12       Impact factor: 22.113

10.  Human erythroid burst-forming unit: T-cell requirement for proliferation in vitro.

Authors:  D G Nathan; L Chess; D G Hillman; B Clarke; J Breard; E Merler; D E Housman
Journal:  J Exp Med       Date:  1978-02-01       Impact factor: 14.307

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  4 in total

1.  Establishment of Tac-negative, interleukin-2-dependent cytotoxic cell lines from large granular lymphocytes (LGL) of patients with expanded LGL populations.

Authors:  V Pistoia; A J Carroll; E F Prasthofer; A B Tilden; K S Zuckerman; M Ferrarini; C E Grossi
Journal:  J Clin Immunol       Date:  1986-11       Impact factor: 8.317

2.  Dependence of highly enriched human bone marrow progenitors on hemopoietic growth factors and their response to recombinant erythropoietin.

Authors:  C A Sieff; S G Emerson; A Mufson; T G Gesner; D G Nathan
Journal:  J Clin Invest       Date:  1986-01       Impact factor: 14.808

3.  Normal human serum stimulates murine erythroid precursor growth in in vitro culture.

Authors:  S Nacol-Lizard; S Arnaud; J P Blanchet
Journal:  Blut       Date:  1987-01

4.  Production of hematopoietic colony-stimulating factors by human natural killer cells.

Authors:  M C Cuturi; I Anegón; F Sherman; R Loudon; S C Clark; B Perussia; G Trinchieri
Journal:  J Exp Med       Date:  1989-02-01       Impact factor: 14.307

  4 in total

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