We and other groups have recently shown that it is possible to convert skin cells from foreskin of newborns into nerve cells that closely resemble nerve cells of the brain in terms of both shape and functional properties. If it were possible to also reprogram human adult skin cells into similarly functional nerve cells, we would be able to generate functional nerve cells from patients that are suffering from a variety of brain diseases. These cells could be used to study the processes underlying these diseases. Furthermore, new skin-derived nerve cells could be used for novel transplantation-based therapies for neurodegenerative diseases such as Parkinson’s disease. It is also conceivable that brain cells other than nerve cells could be converted in the living brain into specific nerve cells that are lost due to the disease process.
However, all these potential translational applications rely on our ability to generate functional nerve cells not only from newborns but also from adult skin cells. Unfortunately, all efforts to convert human adult fibroblasts into mature functional nerve cells have failed thus far. We reason that there must be molecular differences between newborn and adult cells that are responsible for the lack of reprogramming. In this proposal we suggest to identify these molecular blockers of nerve cell reprogramming from adult skin cells, which would enable us to devise methods to overcome these blockers.
The goal of our proposal is to enable the reprogramming of adult human skin cells into fully functional and mature nerve cells. If successful, these reprogrammed nerve cells could be used for a variety of clinical applications. First, such cells could be derived from patients suffering from a variety of neurodegenerative diseases such as Parkinson’s and Alzheimer’s disease but also neurodevelopmental diseases such as Autism, Schizophrenia, or bipolar disease. Such nerve cells could then be used to capture processes that underlie those diseases which would enable us to test ways to block these disease processes such as the testing of small molecule drugs. Another potential use of these cells would be cell transplantation. In particular neurodegenerative diseases (i.e. diseases where neurons are lost) would be good candidate diseases for such an approach as one could attempt to generate nerve cells in the dish and use them to replace those nerve cells that are lost in the brain. Finally, this nerve cell reprogramming method could be used directly in the brain without any cell transplantation. It is conceivable that the delivery of just a handful of reprogramming factors directly into the brain can convert non-nerve cells into new nerve cells that again could take over function of previously lost cells. Our proposal is an important first step towards the realization of these applications that aim to improve the life of people that suffer from incurable disease.
We and other groups have recently shown that it is possible to convert skin cells from foreskin of newborns into nerve cells that closely resemble nerve cells of the brain in terms of both shape and functional properties. However, the reprogramming of adult human skin cells is much less efficient. Therefore there must be some molecular difference between newborn and adult skin cells that causes the different reprogramming efficiency. This proposal is about to identify those differences. We have now after completion of the first year performed a detailed comparison of the two cell types before and after exposure to the reprogramming paradigm. We have now put together a list of factors that may cause the difference and are planning to now evaluate them in a functional way. We also found a critical factor that is actually part of the original factor combination that reprograms skin to nerve cells. This factor's main function seems to be to repress the program that is responsible for the maintenance of the identity of the skin cells.