This sounds like this could lead to some pretty amazing medical science in the (far) future.http://www.physorg.com/news187879295.html#top
1 gene lost = 1 limb regained? Scientists demonstrate mammalian regeneration through single gene deletion
March 15, 2010
A quest that began over a decade ago with a chance observation has reached a milestone: the identification of a gene that may regulate regeneration in mammals. The absence of this single gene, called p21, confers a healing potential in mice long thought to have been lost through evolution and reserved for creatures like flatworms, sponges, and some species of salamander. In a report published today in the Proceedings of the National Academy of Sciences, researchers from The Wistar Institute demonstrate that mice that lack the p21 gene gain the ability to regenerate lost or damaged tissue.
Unlike typical mammals, which heal wounds by forming a scar, these mice begin by forming a blastema, a structure associated with rapid cell growth and de-differentiation as seen in amphibians. According to the Wistar researchers, the loss of p21 causes the cells of these mice to behave more like embryonic stem cells than adult mammalian cells, and their findings provide solid evidence to link tissue regeneration to the control of cell division.
"Much like a newt that has lost a limb, these mice will replace missing or damaged tissue with healthy tissue that lacks any sign of scarring," said the project's lead scientist Ellen Heber-Katz, Ph.D., a professor in Wistar's Molecular and Cellular Oncogenesis program. "While we are just beginning to understand the repercussions of these findings, perhaps, one day we'll be able to accelerate healing in humans by temporarily inactivating the p21 gene."
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I really lack the basics necessary to understand almost everything in there, but here's a link to the article they mention (subscription-only) and the abstract for anyone interested:
link to the article
Lack of p21 expression links cell cycle control and
appendage regeneration in mice
Khamilia Bedelbaeva, Andrew Snyder, Dmitri Gourevitch, Lise Clark, Xiang-Ming Zhang,
John Leferovich, James M. Cheverud, Paul Lieberman, and Ellen Heber-Katz
Abstract
Animals capable of regenerating multiple tissue types, organs, and
appendages after injury are common yet sporadic and include
some sponge, hydra, planarian, and salamander (i.e., newt and
axolotl) species, but notably such regenerative capacity is rare in
mammals. The adult MRL mouse strain is a rare exception to the
rule that mammals do not regenerate appendage tissue. Certain
commonalities, such as blastema formation and basement membrane
breakdown at the wound site, suggest that MRL mice may
share other features with classical regenerators. As reported here,
MRL fibroblast-like cells have a distinct cell-cycle (G2/M accumulation)
phenotype and a heightened basal and wound site DNA
damage/repair response that is also common to classical regenerators
and mammalian embryonic stem cells. Additionally, a neutral
and alkaline comet assay displayed a persistent level of intrinsic
DNA damage in cells derived from the MRL mouse. Similar to
mouse ES cells, the p53-target p21 was not expressed in MRL ear
fibroblasts. Because the p53/p21 axis plays a central role in the
DNA damage response and cell cycle control, we directly tested
the hypothesis that p21 down-regulation could functionally induce
a regenerative response in an appendage of an otherwise nonregenerating
mouse strain. Using the ear hole closure phenotype,
a genetically mapped and reliable quantitative indicator of
regeneration in the MRL mouse, we show that the unrelated
Cdkn1atmi/Tyj/J p21-/- mouse (unlike the B6129SF2/J WT control)
closes ear holes similar to MRL mice, providing a firm link between
cell cycle checkpoint control and tissue regeneration.