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Investigation of NK cell function against two target hematological cell line using radioactive chromium assay.

Authors :
Jurišić V
Source :
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine [Appl Radiat Isot] 2024 Apr; Vol. 206, pp. 111251. Date of Electronic Publication: 2024 Feb 24.
Publication Year :
2024

Abstract

NK (Natural killer) cells are a special population of peripheral blood lymphocytes that kill virus-infected cells as well as tumor cells. For testing NK cell function, the classic gold standard assay has been used for a long time, determining the activity from target tumor cells using radioactive chromium in cell cultures for 4h. In this study two hematological cell lines K562 and MDS where used and target and results showed different sensitivity to killing by NK cells separated from healthy volunteers. Results have been shown that MDS release significantly more radioactive chromium indicating higher degree of necrosis during cell culture. In addition, K562 cell line is better target for NK killing in all different E:T ratio in comparison to MDS cell line previously described. Based on this, it is suggested that K562 cells be continues used in the future as better target for investigation NK killing.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Vladimir Jurisic reports was provided by University of Kragujevac, Serbia. Vladimir Jurisic reports a relationship with University of Kragujevac Faculty of Medical Sciences that includes: employment. Non has patent non pending to non. No any other conflict of Interest.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1872-9800
Volume :
206
Database :
MEDLINE
Journal :
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
Publication Type :
Academic Journal
Accession number :
38422944
Full Text :
https://doi.org/10.1016/j.apradiso.2024.111251