Literature DB >> 2358785

Interleukin 3 perfusion in W/Wv mice allows the development of macroscopic hematopoietic spleen colonies and restores cutaneous mast cell number.

C Ody1, V Kindler, P Vassalli.   

Abstract

The genetically anemic W/Wv mice are characterized by the inability of their bone marrow cells to form macroscopic pluripotent hematopoietic colonies in the spleen of irradiated recipients upon transfer (colony-forming units). Furthermore, they almost totally lack mast cells, notably in the skin. In the present study, we have tested the effect of recombinant murine interleukin 3 (rmIL-3) on W/Wv mice hematopoiesis. Transfer of W/Wv bone marrow cells into lethally irradiated recipients perfused with rmIL-3 is followed by the appearance of macroscopic spleen colonies. Moreover, perfusion of rmIL-3 in W/Wv mice: (a) restores almost normal total numbers of hematopoietic precursors (colony-forming cells), but without modification of anemia; and (b) leads to the appearance of a normal number of mastocytes in the skin.

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Year:  1990        PMID: 2358785      PMCID: PMC2188174          DOI: 10.1084/jem.172.1.403

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  7 in total

1.  Development of rat mast cells in vitro. I. Differentiation of mast cells from thymus cells.

Authors:  T Ishizaka; H Okudaira; L E Mauser; K Ishizaka
Journal:  J Immunol       Date:  1976-03       Impact factor: 5.422

2.  Stimulation of hematopoiesis in vivo by recombinant bacterial murine interleukin 3.

Authors:  V Kindler; B Thorens; S de Kossodo; B Allet; J F Eliason; D Thatcher; N Farber; P Vassalli
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

Review 3.  Hereditary anemias of the mouse: a review for geneticists.

Authors:  E S Russell
Journal:  Adv Genet       Date:  1979       Impact factor: 1.944

4.  Colony formation by primitive hemopoietic progenitor cells in serum-free medium.

Authors:  J F Eliason; N Odartchenko
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

5.  The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene.

Authors:  E N Geissler; M A Ryan; D E Housman
Journal:  Cell       Date:  1988-10-07       Impact factor: 41.582

6.  Growth of factor-dependent hemopoietic precursor cell lines.

Authors:  T M Dexter; J Garland; D Scott; E Scolnick; D Metcalf
Journal:  J Exp Med       Date:  1980-10-01       Impact factor: 14.307

7.  Augmentation of organ-associated natural killer activity by biological response modifiers. Isolation and characterization of large granular lymphocytes from the liver.

Authors:  R H Wiltrout; B J Mathieson; J E Talmadge; C W Reynolds; S R Zhang; R B Herberman; J R Ortaldo
Journal:  J Exp Med       Date:  1984-11-01       Impact factor: 14.307

  7 in total
  3 in total

1.  KIT signaling is dispensable for human mast cell progenitor development.

Authors:  Joakim S Dahlin; Maria Ekoff; Jennine Grootens; Liza Löf; Rose-Marie Amini; Hans Hagberg; Johanna S Ungerstedt; Ulla Olsson-Strömberg; Gunnar Nilsson
Journal:  Blood       Date:  2017-08-08       Impact factor: 22.113

2.  The rat c-kit ligand, stem cell factor, induces the development of connective tissue-type and mucosal mast cells in vivo. Analysis by anatomical distribution, histochemistry, and protease phenotype.

Authors:  M Tsai; L S Shih; G F Newlands; T Takeishi; K E Langley; K M Zsebo; H R Miller; E N Geissler; S J Galli
Journal:  J Exp Med       Date:  1991-07-01       Impact factor: 14.307

3.  Mouse bone marrow-derived mast cells (mBMMC) obtained in vitro from mice that are mast cell-deficient in vivo express the same panel of granule proteases as mBMMC and serosal mast cells from their normal littermates.

Authors:  K K Eklund; N Ghildyal; K F Austen; D S Friend; V Schiller; R L Stevens
Journal:  J Exp Med       Date:  1994-07-01       Impact factor: 14.307

  3 in total

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