Literature DB >> 208982

Mouse natural killer (NK) cell activity against human cell lines is not influenced by superinfection of the target cell with xenotropic murine C-type virus.

R Kiessling, O Haller, E M Fenyö, M Steinitz, G Klein.   

Abstract

Mouse natural killer (NK) cells can lyse a variety of syngeneic, allogeneic and xenogeneic target cells in short-term 51Cr release assays. The target specificity of NK cells is not known, but endogenous C-type viral antigens have been suggested as possible target structures. To test this hypothesis, human lymphoid lines were superinfected with xenotropic mouse C-type virus either by repeated dosage through nude mice or by in vitro superinfection with the supernatants of nude-mouse-passaged lines. The appearance of surface-associated MuLV antigens after superinfection was confirmed in a complement-dependent cytotoxicity test. Subsequently, the NK sensitivity of each infected line was compared with its non-infected counterpart in direct cytolytic and competition assays. None of these two assay systems showed a consistent difference in NK sensitivity of infected and non-infected cell lines. These findings do not lend support to the concept tht murine C-type viral antigens are responsible for NK sensitivity.

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Year:  1978        PMID: 208982     DOI: 10.1002/ijc.2910210410

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  3 in total

1.  Target-effector interaction in the natural killer cell system: isolation of target structures.

Authors:  J C Roder; A Rosén; E M Fenyö; F A Troy
Journal:  Proc Natl Acad Sci U S A       Date:  1979-03       Impact factor: 11.205

2.  Relation of gp70 to spontaneous cytolytic activity of mouse spleen cells.

Authors:  A Hatzfeld; A Pinter; G C Koo; E A Boyse
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

Review 3.  Using mouse models to study function of transcriptional factors in T cell development.

Authors:  Peng Li; Yiren Xiao; Zhixin Liu; Pentao Liu
Journal:  Cell Regen (Lond)       Date:  2012-10-10
  3 in total

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