Literature DB >> 6722038

Long-term haemopoiesis in human fetal liver cell cultures.

M D Cappellini, C G Potter, W G Wood.   

Abstract

Haemopoiesis in human fetal liver is almost entirely restricted to the erythroid series but when fetal liver cells were cultured under conditions established for the long-term maintenance of adult marrow haemopoiesis, a rapid switch to granulopoiesis was observed. Erythroid progenitor cells (BFU-E) rapidly disappeared, even though no humoral or cellular inhibitors of erythropoiesis could be detected, while myeloid progenitors (CFU-GM) increased in number. When the fetal liver cells were seeded onto stromal layers derived from adult marrow, in which endogenous haemopoiesis had ceased, granulopoiesis was established and maintained for more than a year, considerably longer than has previously been achieved with human haemopoietic cells.

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Year:  1984        PMID: 6722038     DOI: 10.1111/j.1365-2141.1984.tb02865.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  4 in total

1.  Soluble factor(s) produced by adult bone marrow stroma inhibit in vitro proliferation and differentiation of fetal liver BFU-E by inducing apoptosis.

Authors:  V Roy; C M Verfaillie
Journal:  J Clin Invest       Date:  1997-08-15       Impact factor: 14.808

2.  A protein factor binding to an octamer motif in the gamma-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cells.

Authors:  R Mantovani; N Malgaretti; B Giglioni; P Comi; N Cappellini; S Nicolis; S Ottolenghi
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

3.  An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoter.

Authors:  R Mantovani; N Malgaretti; S Nicolis; B Giglioni; P Comi; N Cappellini; M T Bertero; F Caligaris-Cappio; S Ottolenghi
Journal:  Nucleic Acids Res       Date:  1988-05-25       Impact factor: 16.971

4.  Human fetal liver cultures support multiple cell lineages that can engraft immunodeficient mice.

Authors:  Marina E Fomin; Ashley I Beyer; Marcus O Muench
Journal:  Open Biol       Date:  2017-12       Impact factor: 6.411

  4 in total

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