Literature DB >> 9176104

Characterization of a mast cell line that lacks the extracellular domain of membrane c-kit.

Y A Mekori1, C K Oh, J Dastych, J P Goff, S Adachi, P J Bianchine, A Worobec, T Semere, J H Pierce, D D Metcalfe.   

Abstract

Expression of the c-kit proto-oncogene receptor on mast cells is essential for their normal proliferation and maturation as well as for several biological responses such as chemotaxis and attachment. In the present study we report that the interleukin-3 (IL-3)-dependent mast cell line CFTL-15 lacks the extracellular domain of the c-kit receptor. This observation was made after noting that the c-kit ligand stem cell factor (SCF) could not prevent IL-3 deprivation-induced mast cell apoptosis and that CFTL-15 cells did not proliferate in response to SCF. Flow cytometric analysis employing monoclonal anti-c-kit antibodies, and immunogold labelling with analysis by electron microscopy, subsequently showed a diminished expression of c-kit on CFTL-15 cells. There was no identifiable message for the extracellular domain of c-kit in these cells, as determined by reverse transcriptase-polymerase chain reaction (RT-PCR). These previously unrecognized properties of the CFTL-15 mast cell line allowed the examination of other biological consequences of the lack of c-kit on mast cells. Analysing the ability of these cells to adhere to surface-bound fibronectin, it was found that addition of SCF did not increase their adhesion to this substrate, in opposition to what is reported with other mast cells. Similarly, CFTL-15 mast cells did not adhere to fibroblasts, which is known to require c-kit expression. Also, there was no protein tyrosine phosphorylation in these cells in response to SCF. CFTL-15 cells underwent apoptosis on removal of IL-3 coincident with a decrease in endogenous Bcl-2 mRNA. Overexpression of Bcl-2 cDNA prolonged survival of Bcl-2-transfected CFTL-15 cells upon withdrawal of IL-3. Thus, the CFTL-15 cell line that lacks surface c-kit is not able to proliferate in response to SCF, undergoes apoptosis in the presence of SCF, and does not adhere to fibroblasts. These results confirm earlier studies on the functional consequences of c-kit and provide a novel experimental model for further investigation.

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Year:  1997        PMID: 9176104      PMCID: PMC1456705          DOI: 10.1046/j.1365-2567.1997.00214.x

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  25 in total

1.  Focal adhesion protein-tyrosine kinase phosphorylated in response to cell attachment to fibronectin.

Authors:  S K Hanks; M B Calalb; M C Harper; S K Patel
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

2.  Mast cell number in the skin of heterozygotes reflects the molecular nature of c-kit mutation.

Authors:  T Tsujimura; U Koshimizu; H Katoh; K Isozaki; Y Kanakura; T Tono; S Adachi; T Kasugai; H Tei; Y Nishimune
Journal:  Blood       Date:  1993-05-15       Impact factor: 22.113

3.  Adhesion of mouse mast cells to fibroblasts: adverse effects of steel (Sl) mutation.

Authors:  Y Kaneko; J Takenawa; O Yoshida; K Fujita; K Sugimoto; H Nakayama; J Fujita
Journal:  J Cell Physiol       Date:  1991-05       Impact factor: 6.384

4.  Immortalization of mouse bone marrow-derived mast cells with Ad12-SV40 virus.

Authors:  N Arora; K U Min; J J Costa; J S Rhim; D D Metcalfe
Journal:  Int Arch Allergy Immunol       Date:  1993       Impact factor: 2.749

5.  Steel factor-induced tyrosine phosphorylation in murine mast cells. Common elements with IL-3-induced signal transduction pathways.

Authors:  M J Welham; J W Schrader
Journal:  J Immunol       Date:  1992-10-15       Impact factor: 5.422

6.  Suppression of apoptosis in a cytotoxic T-cell line by interleukin 2-mediated gene transcription and deregulated expression of the protooncogene bcl-2.

Authors:  G Deng; E R Podack
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-15       Impact factor: 11.205

7.  Necessity of extracellular domain of W (c-kit) receptors for attachment of murine cultured mast cells to fibroblasts.

Authors:  S Adachi; Y Ebi; S Nishikawa; S Hayashi; M Yamazaki; T Kasugai; T Yamamura; S Nomura; Y Kitamura
Journal:  Blood       Date:  1992-02-01       Impact factor: 22.113

8.  The c-kit receptor ligand functions as a mast cell chemoattractant.

Authors:  C J Meininger; H Yano; R Rottapel; A Bernstein; K M Zsebo; B R Zetter
Journal:  Blood       Date:  1992-02-15       Impact factor: 22.113

9.  Ligand stimulation of transfected and endogenous growth factor receptors enhances cytokine production by mast cells.

Authors:  A D Keegan; J H Pierce; J Artrip; M Plaut; W E Paul
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

10.  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

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  5 in total

Review 1.  Importance of mast cells in the pathophysiology of asthma.

Authors:  Seong H Cho; Andrea J Anderson; Chad K Oh
Journal:  Clin Rev Allergy Immunol       Date:  2002-04       Impact factor: 8.667

Review 2.  Mast cell homeostasis and the JAK-STAT pathway.

Authors:  J K Morales; Y T Falanga; A Depcrynski; J Fernando; J J Ryan
Journal:  Genes Immun       Date:  2010-06-10       Impact factor: 2.676

3.  Human mast cell apoptosis is regulated through Bcl-2 and Bcl-XL.

Authors:  Y A Mekori; A M Gilfillan; C Akin; K Hartmann; D D Metcalfe
Journal:  J Clin Immunol       Date:  2001-05       Impact factor: 8.317

4.  Expression of Bcl-2 and Bcl-xL in cutaneous and bone marrow lesions of mastocytosis.

Authors:  Karin Hartmann; Metin Artuc; Stephan E Baldus; Thomas K Zirbes; Barbara Hermes; Juergen Thiele; Yoseph A Mekori; Beate M Henz
Journal:  Am J Pathol       Date:  2003-09       Impact factor: 4.307

5.  Essential role of the prosurvival bcl-2 homologue A1 in mast cell survival after allergic activation.

Authors:  Z Xiang; A A Ahmed; C Möller; K Nakayama; S Hatakeyama; G Nilsson
Journal:  J Exp Med       Date:  2001-12-03       Impact factor: 14.307

  5 in total

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