Radiation induced apoptosis in ataxia telangiectasia homozygote, heterozygote and normal cells
- PMID: 11336979
- DOI: 10.1016/s0027-5107(00)00168-8
Radiation induced apoptosis in ataxia telangiectasia homozygote, heterozygote and normal cells
Abstract
Recent reports suggest that the radiation-induced, p53-dependent, apoptotic response is aberrant in ataxia telangiectasia (AT) cells. We investigated the possibility that an aberrant apoptotic response to ionizing radiation may also be the characteristic of AT heterozygotes and may facilitate in discriminating AT heterozygotes from the general population. Log phase, Epstein Barr virus (EBV) transformed lymphoblastoid cell lines and primary lymphocytes from three AT families were irradiated and the apoptotic response at 30h post radiation was measured by flow cytometry using TUNEL and hypodiploid methods. Our results show that the apoptotic response of AT homozygote (ATM-/-), AT heterozygote (ATM+/-) and normal cells (ATM+/+) to ionizing radiation, measured by the hypodiploid and TUNEL methods using flow cytometry, is dose and time dependent. Furthermore, this response is paradoxical in that ATM (-/-) lymphoblastoid cells were characterized by a reduced post radiation apoptotic response compared to their normal counterparts. Heterozygote (ATM+/-) lymphoblastoid cells displayed an intermediate response to ionizing radiation. In contrast, primary, non-transformed AT cells exhibited the same apoptotic response as their normal counterparts. Our results thus indicate that pre-radiation, EBV-transformed, lymphoblastoid cell lines from individual families may be useful in discriminating ATM status, but patient-derived, primary AT homozygous, heterozygous and normal primary cultured lymphocytes cannot be discriminated by this assay.
Similar articles
-
X-irradiation induces up-regulation of ATM gene expression in wild-type lymphoblastoid cell lines, but not in their heterozygous or homozygous ataxia-telangiectasia counterparts.Jpn J Cancer Res. 2001 Jun;92(6):710-7. doi: 10.1111/j.1349-7006.2001.tb01152.x. Jpn J Cancer Res. 2001. PMID: 11429062 Free PMC article.
-
Individual radiosensitivity does not correlate with radiation-induced apoptosis in lymphoblastoid cell lines or CD3+ lymphocytes.Strahlenther Onkol. 2005 May;181(5):326-35. doi: 10.1007/s00066-005-1372-0. Strahlenther Onkol. 2005. PMID: 15900430
-
Detection of individual differences in radiation-induced apoptosis of peripheral blood lymphocytes in normal individuals, ataxia telangiectasia homozygotes and heterozygotes, and breast cancer patients after radiotherapy.Radiat Res. 2000 May;153(5 Pt 1):570-8. doi: 10.1667/0033-7587(2000)153[0570:doidir]2.0.co;2. Radiat Res. 2000. PMID: 10790278
-
Elevated frequency of p53-independent apoptosis after irradiation increases levels of DNA breaks in ataxia telangiectasia lymphoblasts.Int J Radiat Biol. 1997 Sep;72(3):257-69. doi: 10.1080/095530097143257. Int J Radiat Biol. 1997. PMID: 9298106
-
Epstein-Barr virus-transformed lymphoblastoid cell lines of ataxia telangiectasia patients are defective in X-ray-induced apoptosis.Int J Radiat Biol. 1999 Jun;75(6):709-16. doi: 10.1080/095530099140041. Int J Radiat Biol. 1999. PMID: 10405000
Cited by
-
Analysis of Residual DSBs in Ataxia-Telangiectasia Lymphoblast Cells Initiating Apoptosis.Biomed Res Int. 2016;2016:8279560. doi: 10.1155/2016/8279560. Epub 2016 Jan 6. Biomed Res Int. 2016. PMID: 27057549 Free PMC article.
-
Telomerase activity, apoptosis and cell cycle progression in ataxia telangiectasia lymphocytes expressing TCL1.Br J Cancer. 2003 Sep 15;89(6):1091-5. doi: 10.1038/sj.bjc.6601213. Br J Cancer. 2003. PMID: 12966431 Free PMC article.
-
RADIOSENSITIVITY TO HIGH ENERGY IRON IONS IS INFLUENCED BY HETEROZYGOSITY for ATM, RAD9 and BRCA1.Adv Space Res. 2010 Sep 1;46(6):681-686. doi: 10.1016/j.asr.2010.02.026. Adv Space Res. 2010. PMID: 24431481 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous