Ataxia telangiectasia derived iPS cells show preserved x-ray sensitivity and decreased chromosomal instability

نویسندگان

  • Yoshihiro Fukawatase
  • Masashi Toyoda
  • Kohji Okamura
  • Ken-ichi Nakamura
  • Kazuhiko Nakabayashi
  • Shuji Takada
  • Mayu Yamazaki-Inoue
  • Akira Masuda
  • Michiyo Nasu
  • Kenichiro Hata
  • Kazunori Hanaoka
  • Akon Higuchi
  • Kaiyo Takubo
  • Akihiro Umezawa
چکیده

Ataxia telangiectasia is a neurodegenerative inherited disease with chromosomal instability and hypersensitivity to ionizing radiation. iPS cells lacking ATM (AT-iPS cells) exhibited hypersensitivity to X-ray irradiation, one of the characteristics of the disease. While parental ataxia telangiectasia cells exhibited significant chromosomal abnormalities, AT-iPS cells did not show any chromosomal instability in vitro for at least 80 passages (560 days). Whole exome analysis also showed a comparable nucleotide substitution rate in AT-iPS cells. Taken together, these data show that ATM is involved in protection from irradiation-induced cell death.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2014