Literature DB >> 3091386

A role for the macrophage in normal hemopoiesis. II. Effect of varying physiological oxygen tensions on the release of hemopoietic growth factors from bone-marrow-derived macrophages in vitro.

I N Rich.   

Abstract

The effect of oxygen tensions in the physiological range as an environmental signal on the growth of in vitro murine hemopoietic progenitor cells and the production of hemopoietic growth factors (HGF) from macrophages was investigated. Early (BFU-E) and late (CFU-E) erythroid and granulocyte-macrophage (GM-CFC) progenitor cells were cultured in an atmosphere containing 2%, 3.5%, or 5% oxygen. For both the BFU-E and CFU-E populations, a gas phase containing 3.5% oxygen proved to be optimal, producing greater colony numbers than cultures incubated under 2% or 5% oxygen-tension conditions. For GM-CFC growth, 2% and 3.5% oxygen resulted in a greater stimulation than 5% oxygen. Macrophages derived from unseparated and unstimulated mouse bone marrow cells were cultured on hydrophobic Teflon foils under varying oxygen-tension conditions. The production of erythropoietin (epo), present in the culture supernatants, increased as the oxygen concentration increased from 2% to 3.5%, but then decreased as the oxygen concentration was increased further, from 3.5% to 5%. The presence of a factor demonstrating functional similarity with Interleukin-3 was produced optimally under 5% oxygen-tension conditions. The production of granulocyte-macrophage colony-stimulating factor (GM-CSF) was not significantly affected by changing the oxygen-tension conditions. These results demonstrate that physiological oxygen tension plays an important role not only in the growth of hemopoietic progenitor cells, but also as a physiochemical signal that macrophages can sense and respond to in order to regulate the production of specific secretory products.

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Year:  1986        PMID: 3091386

Source DB:  PubMed          Journal:  Exp Hematol        ISSN: 0301-472X            Impact factor:   3.084


  6 in total

1.  Modeling pO(2) distributions in the bone marrow hematopoietic compartment. II. Modified Kroghian models.

Authors:  D C Chow; L A Wenning; W M Miller; E T Papoutsakis
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

2.  No detection of macrophage erythropoietin production in bone marrow from rheumatoid arthritis patients with and without anaemia and controls.

Authors:  G Vreugdenhil; P J Coppens; B Lowenberg; A J Swaak
Journal:  Clin Rheumatol       Date:  1991-12       Impact factor: 2.980

Review 3.  The role of erythropoietin in the anaemia of chronic disease in rheumatoid arthritis.

Authors:  G Vreugdenhil; A J Swaak
Journal:  Clin Rheumatol       Date:  1990-03       Impact factor: 2.980

4.  Intraperitoneal production of erythropoietin with continuous ambulatory peritoneal dialysis.

Authors:  M Chandra; G Clemons; I Sahdev; M McVicar; P Bluestone
Journal:  Pediatr Nephrol       Date:  1993-06       Impact factor: 3.714

5.  The expression of embryonic globin mRNA in a severely anemic mouse model induced by treatment with nitrogen-containing bisphosphonate.

Authors:  Hirotada Otsuka; Jiro Takito; Yasuo Endo; Hideki Yagi; Satoshi Soeta; Nobuaki Yanagisawa; Naoko Nonaka; Masanori Nakamura
Journal:  BMC Hematol       Date:  2016-02-11

6.  Hypoxic conditions increase hypoxia-inducible transcription factor 2alpha and enhance chondrogenesis in stem cells from the infrapatellar fat pad of osteoarthritis patients.

Authors:  Wasim S Khan; Adetola B Adesida; Timothy E Hardingham
Journal:  Arthritis Res Ther       Date:  2007       Impact factor: 5.156

  6 in total

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