Irvine, Calif., Oct. 24, 2013 — Cells triggering tissue regeneration that are taken from one limb and grafted onto another acquire the molecular "fingerprint," or identity, of their new location, UC Irvine developmental biologists have discovered.
The findings provide a better understanding of how grafted tissue changes its identity to match the host tissue environment during the process of limb regeneration and bring scientists closer to establishing regenerative therapies for humans. The results also challenge the conventional assumption in regeneration biology that cellular properties are predetermined.
By examining cells from blastema tissue in salamanders – amphibians that can regrow lost limbs – the researchers learned that grafted tissue does not spur growth of structures consistent with the region of the limb it came from, but rather it transforms into the cell signature of the limb region it's been grafted onto. This ability of cells to alter identity from the old location to the new location is called positional plasticity.
"This work provides the first piece of molecular evidence supporting the idea that early- and late-stage blastema cells receive information about the 'blueprint' of the missing limb from the host site," said Catherine D. McCusker, postdoctoral fellow in developmental & cell biology and lead author on the study.
The blastema is a group of cells that accumulate at the site of a severed limb in organisms such as salamanders and re-create the missing appendage. It's formed when regenerating nerve fibers from the limb stump interact with thin skin that covers the surface of the wound.
This interaction attracts cells from the stump tissue that undergo a process called dedifferentiation, in which the cells revert to a more embryonic state. Once a blueprint of the missing limb structures is established in the blastema, these cells gradually differentiate into the replacement limb.
In her study, McCusker found that signals from nerve fibers played a crucial role in sustaining the cells' ability to change their identity to suit a new environment throughout the course of regeneration. She hypothesizes that it's important for the nerve fibers to maintain positional plasticity in the blastema until a complete blueprint of the new limb is formulated.
These findings also have potential implications in cancer biology, as cancer cells too are strongly influenced by the surrounding tissue environment.
"Our study shows that the blueprint, which drives the behavior of cells, can be manipulated," McCusker noted. "Thus, understanding how differing environments affect blastema cell behavior will provide valuable insight into how to control the behavior of cancer cells."
To access the study, which appeared in the Sept. 27 issue of the open-access journal PLOS ONE, go to http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0077064.
David M. Gardiner, professor of developmental & cell biology at UC Irvine, also contributed to the study, supported by the U.S. Army Research Office Multidisciplinary University Research Initiative (TUL 589-09/10). McCusker's work was supported by a postdoctoral fellowship from the American Cancer Society (PF-12-145-01-DDC).
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Contact:
Andrea Burgess
949-824-6282
andrea.burgess@uci.edu
Journal
PLOS ONE