Hair, bone and soft tissue regrown in mice by enhancing cell metabolism
Anyone who has left youth behind them knows that bumps and scrapes don't heal as fast as they used to. But that could change with researchers at the Stem Cell Program at Boston Children's Hospital finding a way to regrow hair, cartilage, bone, skin and other soft tissues in a mouse by reactivating a dormant gene called Lin28a. The discovery could lead to new treatments that provide adults with the regenerative powers they possessed when very young.
Lin28 is a gene that is abundant in embryonic stem cells and which functions in all organisms. It is thought to regulate the self-renewal of stem cells with the researchers finding that by promoting the production of certain enzymes in mitochondria, it enhances the metabolism of these cellular power plants that found in most of the cells of living organisms. In this way, Lin28 helps generate the energy needed to stimulate the growth of new tissues.
"We already know that accumulated defects in mitochondrial metabolism can lead to aging in many cells and tissues," says Shyh-Chang Ng. "We are showing the converse – that enhancement of mitochondrial metabolism can boost tissue repair and regeneration, recapturing the remarkable repair capacity of juvenile animals."
"Most people would naturally think that growth factors are the major players in wound healing, but we found that the core metabolism of cells is rate-limiting in terms of tissue repair," adds Shyh-Chang. "The enhanced metabolic rate we saw when we reactivated Lin28a is typical of embryos during their rapid growth phase."
The team found that it was also possible to enhance wound healing without reactivating Lin28 but by directly activating mitochondrial metabolism using a small-molecule compound. The team say this suggests it should be possible to develop drugs that promote tissue repair.
But reactivating Lin28 didn't produce the same results across the board. Although they were even able to enhance the regrowth of fingertips in newborn mice, this wasn't achieved in adult mice. There was also little effect on heart tissue.
"Lin28a could be a key factor in constituting a healing cocktail," says Shyh-Chang, "but there are other embryonic factors that remain to be found."
The team, which was led by George Q. Daley, MD, PhD, has published their findings in the journal Cell.
Source: Boston Children's Hospital