A two-stage, p16INK4A- and p53-dependent keratinocyte senescence mechanism that limits replicative potential independent of telomere status

James G. Rheinwald, William C. Hahn, Matthew R. Ramsey, Jenny Y. Wu, Zongou Guo, Hensin Tsao, Michele De Luca, Caterina Catricalà, Kathleen M. O'Toole

Research output: Contribution to journalArticle

259 Citations (Scopus)

Abstract

With increasing frequency during serial passage in culture, primary human keratinocytes express p16INK4A (p16) and undergo senescence arrest. Keratinocytes engineered to express hTERT maintain long telomeres but typically are not immortalized unless, by mutation or other heritable event, they avoid or greatly reduce p16 expression. We have confirmed that keratinocytes undergo p16-related senescence during growth in culture, whether in the fibroblast feeder cell system or in the specialized K-sfm medium formulation, and that this mechanism can act as a barrier to immortalization following hTERT expression. We have characterized the p16-related arrest mechanism more precisely by interfering specifically with several regulators of cell cycle control. Epidermal, oral mucosal, corneal limbal, and conjunctival keratinocytes were transduced to express a p16-insensitive mutant cdk4 (cdk4R24C), to abolish p16 control, and/or a dominant negative mutant p53 (p53DD), to abolish p53 function. Expression of either cdk4R24C or p53DD alone had little effect on life span, but expression of both permitted cells to divide 25 to 43 population doublings (PD) beyond their normal limit. Keratinocytes from a p16+/- individual transduced to express p53DD alone displayed a 31-PD life span extension associated with selective growth of variants that had lost the wild-type p16 allele. Cells in which both p53 and p16 were nonfunctional divided rapidly during their extended life span but experienced telomere erosion and ultimately ceased growth with very short telomeres. Expression of hTERT in these cells immortalized them. Keratinocytes engineered to express cdk4R24C and hTERT but not p53DD did not exhibit an extended life span. Rare immortal variants exhibiting p53 pathway defects arose from them, however, indicating that the p53-dependent component of keratinocyte senescence is telomere independent. Mutational loss of p16 and p53 has been found to be a frequent early event in the development of squamous cell carcinoma. Our results suggest that such mutations endow keratinocytes with extended replicative potential which may serve to increase the probability of neoplastic progression.

Original languageEnglish
Pages (from-to)5157-5172
Number of pages16
JournalMolecular and Cellular Biology
Volume22
Issue number14
DOIs
Publication statusPublished - 2002

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Telomere
Keratinocytes
Growth
Serial Passage
Feeder Cells
Mutation
Life Expectancy
Cell Cycle Checkpoints
Population
Squamous Cell Carcinoma
Fibroblasts
Alleles

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cell Biology

Cite this

A two-stage, p16INK4A- and p53-dependent keratinocyte senescence mechanism that limits replicative potential independent of telomere status. / Rheinwald, James G.; Hahn, William C.; Ramsey, Matthew R.; Wu, Jenny Y.; Guo, Zongou; Tsao, Hensin; De Luca, Michele; Catricalà, Caterina; O'Toole, Kathleen M.

In: Molecular and Cellular Biology, Vol. 22, No. 14, 2002, p. 5157-5172.

Research output: Contribution to journalArticle

Rheinwald, JG, Hahn, WC, Ramsey, MR, Wu, JY, Guo, Z, Tsao, H, De Luca, M, Catricalà, C & O'Toole, KM 2002, 'A two-stage, p16INK4A- and p53-dependent keratinocyte senescence mechanism that limits replicative potential independent of telomere status', Molecular and Cellular Biology, vol. 22, no. 14, pp. 5157-5172. https://doi.org/10.1128/MCB.22.14.5157-5172.2002
Rheinwald, James G. ; Hahn, William C. ; Ramsey, Matthew R. ; Wu, Jenny Y. ; Guo, Zongou ; Tsao, Hensin ; De Luca, Michele ; Catricalà, Caterina ; O'Toole, Kathleen M. / A two-stage, p16INK4A- and p53-dependent keratinocyte senescence mechanism that limits replicative potential independent of telomere status. In: Molecular and Cellular Biology. 2002 ; Vol. 22, No. 14. pp. 5157-5172.
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