U. SHEFFIELD (UK) — Computer models suggest that “sleeping” skin cells are responsible for skin’s ability to regenerate—or not.
Researchers developed an “in silico” (computer) model of human skin biology, capturing how the outer layers of the skin are developed and maintained over time. The “virtual” skin was then used to test the three most popular theories of how skin cells function to regenerate our skin, the largest human organ, over a three-year period.
When the simulation was run according to two of the theories, the virtual skin failed to fully regenerate. Only one theory enabled the virtual skin to still be in good shape after three years, as Xinshan Li of the University of Sheffield in the Faculty of Engineering and Arun Upadhyay of the Procter & Gamble Company explain in research published in Nature Scientific Reports.
“The theory which seems to fit best says that skin has a population of ‘sleeping’ stem cells, which sit in the lowest layer of the skin but don’t constantly divide to make new cells,” Li says. “However, these sleeping cells can be called into action if the skin is damaged, or if the numbers of other types of more mature skin cells decrease, ensuring that the skin can be constantly regenerated under all conditions.”
The model showed that we gradually lose these sleeping stem cells over time, which would explain why our ability to regenerate our skin reduces as we age.
“Each time we wake up these cells, to heal a wound or replenish stocks of other cells, a few of them don’t go back into sleep mode, so the population slowly reduces,” says Li.
“This explains why older skin is slower to heal and in part why our skin changes as we age. By understanding this mechanism better, it might be possible to find ways to combat the effects of aging on our skin.”
Computer modeling of skin biology is the latest step in the evolution of skin science. It allows scientists to project the activity of tissues like skin that are difficult to follow in live systems for extended periods.
Currently, 3D cultures of engineered human skin are viable for only a few weeks and clinical studies in humans are only practical for a few months. With the development of in silico models scientists can predict for the first time what happens in skin over years and even over decades.
“These models permit exploration of hypotheses in very short periods of time, relative to the lab based bench work,” says Upadhyay. “In silico modeling can significantly shorten research and development programs, and help focus subsequent lab or clinical work on the options with the greatest likelihood of succeeding. This is another reason why in silico models are an effective complement to more established research tools and methods.”
The ability to follow virtual skin models over decades may be especially important to skin cancer research. Environmental damage caused by UV exposure or chronic wounding can cause sleeping cells to harbor the mutations which cause skin cancers such as basal cell carcinoma, a very aggressive type of skin cancer.
“The stem cells can harbor mutations over years, but with no effect if they’re still in sleep mode,” explains Li. “However, when they start to divide to heal a wound for example, this could trigger the cancer. If it’s possible to study this phenomenon over long periods of time it may be possible to find ways to prevent the activation of mutated cells and so reduce the risk of developing the disease.”
Other parts of the body, such as the lung or gut lining and the cornea, also regenerate in the same way as our skin. Research is already under way to look at the healing process of the lung lining following asthma attacks.
Upadhyay summarizes the study noting that “you really don’t understand something until you have built it from scratch. By building the virtual skin model from a few cells into a tissue capable of self-renewal, we have moved a big step in our understanding of stem cells and skin renewal.”
Source: University of Sheffield