The JAM test. A simple assay for DNA fragmentation and cell death
- PMID: 1765650
- DOI: 10.1016/0022-1759(91)90325-a
The JAM test. A simple assay for DNA fragmentation and cell death
Abstract
Most current methods for measuring cell death are based on plasma membrane disintegration and the consequent release of cytoplasm. The relevant cells are usually loaded with a label (usually 51Cr or 125I), the release of which is measured. I describe here a method, based on the recent evidence that dying cells often degrade their DNA into small fragments, which measures the DNA retained by living cells rather than the cellular components lost by dying cells. The assay is set up essentially like the current cell lysis assays and harvested like a cell proliferation assay. It is faster, more sensitive, easier to set up, less expensive and safer than the current standard 51Cr release assay.
Similar articles
-
The JAM Test and its daughter P-JAM: simple tests of DNA fragmentation to measure cell death and stasis.Nat Protoc. 2006;1(2):672-82. doi: 10.1038/nprot.2006.107. Nat Protoc. 2006. PMID: 17406295
-
Comparison of fluorochrome-labeled and 51Cr-labeled targets for natural killer cytotoxicity assay.J Immunol Methods. 1989 Aug 15;122(1):15-24. doi: 10.1016/0022-1759(89)90329-3. J Immunol Methods. 1989. PMID: 2760476
-
Apoptosis detection by annexin V binding: a novel method for the quantitation of cell-mediated cytotoxicity.J Immunol Methods. 1998 Aug 1;217(1-2):61-70. doi: 10.1016/s0022-1759(98)00090-8. J Immunol Methods. 1998. PMID: 9776575
-
The JAM-assay: optimized conditions to determine death-receptor-mediated apoptosis.Methods. 2003 Oct;31(2):127-34. doi: 10.1016/s1046-2023(03)00122-1. Methods. 2003. PMID: 12957570
-
Cell death mediated by alloreactive cytotoxic T cells via the granule exocytosis or the Fas pathway is independent of p34cdc2 kinase: Fas dependent killing of cells arrested in the cell cycle.Immunol Cell Biol. 2001 Jun;79(3):264-73. doi: 10.1046/j.1440-1711.2001.01008.x. Immunol Cell Biol. 2001. PMID: 11380680
Cited by
-
Murine cytomegalovirus m02 gene family protects against natural killer cell-mediated immune surveillance.J Virol. 2002 Jan;76(2):885-94. doi: 10.1128/jvi.76.2.885-894.2002. J Virol. 2002. PMID: 11752177 Free PMC article.
-
In vitro induction of anterior gradient-2-specific cytotoxic T lymphocytes by dendritic cells transduced with recombinant adenoviruses as a potential therapy for colorectal cancer.Exp Mol Med. 2012 Jan 31;44(1):60-7. doi: 10.3858/emm.2012.44.1.006. Exp Mol Med. 2012. PMID: 22089087 Free PMC article.
-
Fas ligand expression by astrocytoma in vivo: maintaining immune privilege in the brain?J Clin Invest. 1997 Mar 15;99(6):1173-8. doi: 10.1172/JCI119273. J Clin Invest. 1997. PMID: 9077524 Free PMC article.
-
Predominance of CD4 Th1 and CD8 Tc1 cells revealed by characterization of the cellular immune response generated by immunization with a DNA vaccine containing a Trypanosoma cruzi gene.Infect Immun. 1999 Aug;67(8):3855-63. doi: 10.1128/IAI.67.8.3855-3863.1999. Infect Immun. 1999. PMID: 10417149 Free PMC article.
-
Peptide vaccine given with a Toll-like receptor agonist is effective for the treatment and prevention of spontaneous breast tumors.Cancer Res. 2007 Feb 1;67(3):1326-34. doi: 10.1158/0008-5472.CAN-06-3290. Cancer Res. 2007. PMID: 17283170 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources