Literature DB >> 15369136

A GFP-transfected HFWT cell line, GHINK-1, as a novel target for non-RI activated natural killer cytotoxicity assay.

Hideki Harada1, Kaoru Saijo, Isamu Ishiwata, Tadao Ohno.   

Abstract

An anchorage-dependent Wilms' tumor cell line, HFWT, has been found to be extremely susceptible to human natural killer (NK) cells. Here we established a transfectant of HFWT with the green fluorescence protein (GFP) gene, designated GHINK-1 cells, to apply to the activated NK cytotoxicity assay without radioisotope labeling. After being co-cultured with CD3 CD56+ NK cells, GHINK-1 cells released GFP into the medium. The intensity of the fluorescence from the released GFP correlated almost exactly with the radioactivity of a standard 51Cr-release assay performed with suspension-cultured K562 cells. Because it does not require separation of the remaining live target cells by centrifugation, the non-radioisotopic GFP release assay with GHINK-1 cells is a convenient alternative for monitoring human activated NK killing activity.

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Year:  2004        PMID: 15369136     DOI: 10.1111/j.1749-0774.2004.tb00019.x

Source DB:  PubMed          Journal:  Hum Cell        ISSN: 0914-7470            Impact factor:   4.174


  11 in total

1.  A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity.

Authors:  Wannee Kantakamalakul; Jiraporn Jaroenpool; Kovit Pattanapanyasat
Journal:  J Immunol Methods       Date:  2003-01-15       Impact factor: 2.303

2.  A simple and sensitive flow cytometric assay for the determination of the cytotoxic activity of human natural killer cells.

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Journal:  J Immunol Methods       Date:  1990-12-31       Impact factor: 2.303

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Authors:  K Blomberg; R Hautala; J Lövgren; V M Mukkala; C Lindqvist; K Akerman
Journal:  J Immunol Methods       Date:  1996-06-21       Impact factor: 2.303

4.  A fluorescence-based assay for quantitation of lymphokine-activated killer cell activity.

Authors:  T Volgmann; A Klein-Struckmeier; H Mohr
Journal:  J Immunol Methods       Date:  1989-04-21       Impact factor: 2.303

5.  Green fluorescent protein as a marker for gene expression.

Authors:  M Chalfie; Y Tu; G Euskirchen; W W Ward; D C Prasher
Journal:  Science       Date:  1994-02-11       Impact factor: 47.728

6.  A feasible method for expansion of peripheral blood lymphocytes by culture with immobilized anti-CD3 monoclonal antibody and interleukin-2 for use in adoptive immunotherapy of cancer patients.

Authors:  T Sekine; H Shiraiwa; T Yamazaki; K Tobisu; T Kakizoe
Journal:  Biomed Pharmacother       Date:  1993       Impact factor: 6.529

7.  Enzyme release assay of human NK cell activity using beta-galactosidase-expressing K562 target cell line.

Authors:  H Ohmori; H Ikeda; T Tanigawa; T Takai; M Hikida
Journal:  J Immunol Methods       Date:  1993-08-26       Impact factor: 2.303

8.  Carcinoembryonic proteins produced by Wilms' tumor cells in vitro and in vivo.

Authors:  I Ishiwata; I Ono; C Ishiwata; M Soma; T Nakaguchi; K Ohara; M Hirano; H Ishikawa
Journal:  Exp Pathol       Date:  1991

9.  Induction of human autologous cytotoxic T lymphocytes on formalin-fixed and paraffin-embedded tumour sections.

Authors:  S Q Liu; K Saijo; T Todoroki; T Ohno
Journal:  Nat Med       Date:  1995-03       Impact factor: 53.440

10.  Selective expansion of human natural killer cells from peripheral blood mononuclear cells by the cell line, HFWT.

Authors:  Hideki Harada; Kaoru Saijo; Satoru Watanabe; Koji Tsuboi; Tadao Nose; Isamu Ishiwata; Tadao Ohno
Journal:  Jpn J Cancer Res       Date:  2002-03
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