- Hayflick limit
The Hayflick limit is the number of times a cell will divide before it stops due to the telomere reaching a critical length [cite journal
author=Hayflick L.
title= The limited in vitro lifetime of human diploid cell strains.
journal=Exp. Cell Res.
year=1965
volume=37
issue=3
pages=614-636
pmid= 14315085
doi=10.1016/0014-4827(65)90211-9] .It was discovered by
Leonard Hayflick in1965 , at theUniversity of California, San Francisco (UCSF), when Hayflick demonstrated that normal human cells in a cell culture divide about 52 times in 20% oxygen (i.e. practically normal air) or 70 times in 3% oxygen (which is the same as human internal conditions). It then enters a senescence phase (refuting the contention byAlexis Carrel that normal cells are immortal). Eachmitosis shortens thetelomere appendix on the DNA of the cell, thus ticking back an "inner clock" for each subsequent copy of the cell. Some organisms' cells do not encounter the Hayflick limit due to telomere lengthening, examples are long-lived sea-birds, whose cells are technically immortal.This mechanism is believed to have evolved primarily to protect the body from creating a potentially-cancerous cell. Because of the fragmented way
DNA replicates, a very short telomered cell may lead to genomic instability when the proteins meant to be located on the telomere will fail to attach and it will be marked as a double-strand DNA break, possibly leading tocancer .Many
stem cell s, as they are undifferentiated, are not affected by the Hayflick limit. They exist in every tissue and may continue reproducing for the lifespan of the organism. To avoid reaching the barrier, cells that need to keep on dividing express thetelomerase enzyme or use Alternative Lengthening of Telomeres mechanism. These methods are also used by cancer cells to divide uninhibited.The normal Hayflick limit of cells in organisms other than humans varies, and affects their life span.
Carnosine can increase the Hayflick limit in humanfibroblasts [cite journal
author=McFarlan GA.
coauthors=Holliday R.
title=Retardation of the senescence of cultured human fibroblasts by carnosine
journal=Exp. Cell Res.
volume=212
issue=2
pages=167-175
year=1994
pmid=8187813
doi=10.1006/excr.1994.1132] . It appears to reduce the telomere shortening rate as well [cite journal
author=Shao L
coauthors=Li QH, Tan Z
title=L-carnosine reduces telomere damage and shortening rate in cultured normal fibroblasts.
journal= Biochem Biophys Res Commun.
year=2004
volume=324
issue=2
pages=931-936
pmid=15474517
doi10.1016/j.bbrc.2004.09.136] .ee also
*
Apoptosis
*Biological immortality
*HeLa cellsExternal links
[http://www.newscientist.com/article/mg19626255.600-chromosome-caps-may-explain-cell-immortality.html Cell immortality and cancer]
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