Published December 24, 2004 | Version v1
Journal article

Cellular aging of mitochondrial DNA-depleted cells

  • 1. Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong Kangnam-ku, Seoul 135-710 (Korea, Republic of)
  • 2. Asan Institute for Life Sciences, University of Ulsan, 388 Pungnap-dong, Songpa-ku, Seoul 138-736 (Korea, Republic of)
  • 3. Department of Cancer Genetics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 1426 (United States)

Description

We have reported that mitochondrial DNA-depleted ρ0 cells are resistant to cell death. Because aged cells have frequent mitochondrial DNA mutations, the resistance of ρ0 cells against cell death might be related to the apoptosis resistance of aged cells and frequent development of cancers in aged individuals. We studied if ρ0 cells have features simulating aged cells. SK-Hep1 hepatoma ρ0 cells showed typical morphology associated with aging such as increased size and elongated appearance. They had increased senescence-associated β-Gal activity, lipofuscin pigment, and plasminogen activator inhibitor-1 expression. Consistent with their decreased proliferation, the expression of mitotic cyclins was decreased and that of cdk inhibitors was increased. Rb hypophosphorylation and decreased telomerase activity were also noted. Features simulating aged cells were also observed in MDA-MB-435 ρ0 cells. These results support the mitochondrial theory of aging, and suggest that ρ0 cells could serve as an in vitro model for aged cells

Additional details

Identifiers

DOI
10.1016/j.bbrc.2004.10.182;
PII
S0006-291X(04)02480-5;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
325
Journal Issue
4
Journal Page Range
p. 1399-1405
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.