Literature DB >> 7686845

Expression and function of c-Kit in fetal hemopoietic progenitor cells: transition from the early c-Kit-independent to the late c-Kit-dependent wave of hemopoiesis in the murine embryo.

M Ogawa1, S Nishikawa, K Yoshinaga, S Hayashi, T Kunisada, J Nakao, T Kina, T Sudo, H Kodama, S Nishikawa.   

Abstract

The protooncogene c-kit encodes a receptor type tyrosine kinase and is allelic with the W locus of mice. SLF, the c-Kit ligand which is encoded by the Sl locus, has growth promoting activity for hemopoietic stem cells. Previous studies demonstrated that c-Kit is functionally required for the proliferation of hemopoietic progenitor cells at various differentiation stages in adult bone marrow. However, the absence of functional SLF and c-Kit in fetuses with mutant alleles of Sl and W loci produces only minor effects on the myeloid and early erythroid progenitor cells in the fetal liver, although the level of the late erythroid progenitor cells is significantly affected. We used an anti-c-Kit monoclonal antibody to investigate the expression and function of c-Kit in murine fetal hemopoietic progenitor cells. Flow-cytometric analysis showed that hemopoiesis in the yolk sac and fetal liver started from cells that express c-Kit. The c-Kit expression decreased upon maturation into erythrocytes in each organ. By fluorescence activated cell sorting, the c-Kit+ cell population was enriched with the hemopoietic progenitor cells clonable in vitro (CFU-E, BFU-E and GM-CFC). To elucidate whether c-Kit functions in these progenitor cells in vivo, we took advantage of the antagonistic anti-c-Kit monoclonal antibody, ACK2, which can block the function of c-Kit. Administration of ACK2 after 12.5 days of gestation rapidly eliminated BFU-E and GM-CFC as well as CFU-E from the fetal liver. However, the number of these progenitor cells in the yolk sac and fetal liver was less affected when the fetuses were given ACK2 before 12.5 days of gestation. Our results provide evidence that there are two waves of hemopoiesis in murine embryos relative to c-Kit dependency. The c-Kit has an essential role on the growth of hemopoietic progenitor cells in the fetal liver after 12.5 days of gestation, whereas the progenitor cells in the liver and yolk sac of the earlier embryo do not depend on c-Kit and its ligand SLF.

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Year:  1993        PMID: 7686845     DOI: 10.1242/dev.117.3.1089

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  24 in total

1.  Immature erythroblasts with extensive ex vivo self-renewal capacity emerge from the early mammalian fetus.

Authors:  Samantha J England; Kathleen E McGrath; Jenna M Frame; James Palis
Journal:  Blood       Date:  2010-12-02       Impact factor: 22.113

2.  Maturation and enucleation of primitive erythroblasts during mouse embryogenesis is accompanied by changes in cell-surface antigen expression.

Authors:  Stuart T Fraser; Joan Isern; Margaret H Baron
Journal:  Blood       Date:  2006-08-29       Impact factor: 22.113

3.  Kit transduced signals counteract erythroid maturation by MAPK-dependent modulation of erythropoietin signaling and apoptosis induction in mouse fetal liver.

Authors:  N Haas; T Riedt; Z Labbaf; K Baßler; D Gergis; H Fröhlich; I Gütgemann; V Janzen; H Schorle
Journal:  Cell Death Differ       Date:  2014-10-17       Impact factor: 15.828

Review 4.  In vitro differentiation of murine embryonic stem cells. New approaches to old problems.

Authors:  M J Weiss; S H Orkin
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

5.  Prolongation of cardiac allograft survival by a novel population of autologous CD117+ bone marrow-derived progenitor cells.

Authors:  T J Grazia; R J Plenter; H M Lepper; F Victorino; S D Miyamoto; J T Crossno; B A Pietra; R G Gill; M R Zamora
Journal:  Am J Transplant       Date:  2010-11-29       Impact factor: 8.086

6.  Ectodermally derived steel/stem cell factor functions non-cell autonomously during primitive erythropoiesis in Xenopus.

Authors:  Devorah C Goldman; Linnea K Berg; Michael C Heinrich; Jan L Christian
Journal:  Blood       Date:  2005-12-15       Impact factor: 22.113

7.  Rhythmic Cl- current and physiological roles of the intestinal c-kit-positive cells.

Authors:  N Tokutomi; H Maeda; Y Tokutomi; D Sato; M Sugita; S Nishikawa; S Nishikawa; J Nakao; T Imamura; K Nishi
Journal:  Pflugers Arch       Date:  1995-12       Impact factor: 3.657

Review 8.  Extrinsic regulation of hematopoietic stem cells in development, homeostasis and diseases.

Authors:  Yeojin Lee; Matthew Decker; Heather Lee; Lei Ding
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2017-05-31       Impact factor: 5.814

9.  C-kit(+) cells isolated from developing kidneys are a novel population of stem cells with regenerative potential.

Authors:  Erika B Rangel; Samirah A Gomes; Raul A Dulce; Courtney Premer; Claudia O Rodrigues; Rosemeire M Kanashiro-Takeuchi; Behzad Oskouei; Decio A Carvalho; Phillip Ruiz; Jochen Reiser; Joshua M Hare
Journal:  Stem Cells       Date:  2013-08       Impact factor: 6.277

10.  Expression of the LIM-homeobox gene LH2 generates immortalized steel factor-dependent multipotent hematopoietic precursors.

Authors:  P Pinto do O; A Kolterud; L Carlsson
Journal:  EMBO J       Date:  1998-10-01       Impact factor: 11.598

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