Interestingness: 4
By Izumi Horikawa, Toshio Yawata, and J Carl Barrett in the Journal of Anti-Aging Medicine, Volume 3, Issue 4, 2000 (pp 373-382, doi:10.1089/rej.1.2000.3.373.)
Not all cells given telomerase escape senescence and cells with active telomerase can be made to senesce in lots of ways. The p16INK4A/RB pathway can trigger senescence as well as the p14ARF/MDM2/p53 pathway. p53 is probably related to telomeres but other parts probably aren't. By introducing single chromosomes into immortal cancer cell-lines and making them senesce, they infer the existence of other independent pathways of senescence. The mechanisms that trigger senescence are cell-type dependent.
Interesting factoid: mouse cells senesce after much fewer replications (10-20 vs 50-80) even though much longer telomeres.
Thursday, December 29, 2011
Cellular Senescence Mechanisms Independent of Telomere Shortening and Telomerase: Other Barriers to Cell Immortalization and Carcinogenesis
Labels:
4,
P14ARF,
p16INK4A,
p53,
senescence,
telomerase,
telomere
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