How Do Stem Cells Determine What Tissue To Become?
Within 24 hours of culturing adult human stem cells on a new type of matrix, University of Michigan researchers were able to make predictions about how the cells would differentiate, or what type of tissue they would become. Their results are published in the Aug. 1 edition of Nature Methods.
Differentiation is the process of stem cells morphing into other types of cells. Understanding it is key to developing future stem cell-based regenerative therapies.
“We show, for the first time, that we can predict stem cell differentiation as early as Day 1,” said Jianping Fu, an assistant professor in mechanical engineering and biomedical engineering who is the first author on the paper.
“Normally, it takes weeks or maybe longer to know how the stem cell will differentiate. Our work could speed up this lengthy process and could have important applications in drug screening and regenerative medicine. Our method could provide early indications of how the stem cells are differentiating and what the cell types they are becoming under a new drug treatment.”
In this study, Fu and his colleagues examined stem cell mechanics, the slight forces the cells exert on the materials they are attached to. These traction forces were suspected to be involved in differentiation, but they have not been as widely studied as the chemical triggers. In this paper, the researchers show that the stiffness of the material on which stem cells are cultivated in a lab does, in fact, help to determine what type of cells they turn into.
“Our research confirms that mechanical factors are as important as the chemical factors regulating differentiation,” Fu said. “The mechanical aspects have, until now, been largely ignored by stem cell biologists.”
The researchers built a novel type of stem cell matrix, or scaffold, whose stiffness can be adjusted without altering its chemical composition, which cannot be done with conventional stem cell growth matrices, Fu said.
The new scaffold resembles an ultrafine carpet of “microposts,” hair-like projections made of the elastic polymer polydimethylsiloxane—a key component in Silly Putty, Fu said. By adjusting the height of the microposts, the researchers were able to adjust the rigidity of the matrix.
In this experiment, the engineers used human mesenchymal stem cells, which are found in bone marrow and other connective tissues such as fat. The stem cells differentiated into bone when grown on stiffer scaffolds, and into fat when grown on more flexible scaffolds.
Once the researchers observed the cells differentiating according to the mechanical stiffness of the substrate, they decided to measure the cellular traction forces throughout the culturing process to see if they could predict how the cells would differentiate.
Using a technique called fluorescent microscopy, the researchers measured the bending of the microposts in order to quantify the traction forces.
“Our study shows that if the stem cells determine to differentiate into one cell type then their traction forces can be much greater than the ones that do not differentiate, or that differentiate into another cell type,” Fu said. “We prove that we can use the evolution of the traction force as early indicators for stem cell differentiation.”
The new matrix—manufactured through an inexpensive molding process—is so cheap to make that the researchers are giving it away to any interested scientists or engineers.
“We think this toolset provides a newly accessible, practical methodology for the whole community,” Fu said.
The paper is called “Mechanical regulation of cell function using geometrically modulated elastomeric substrates.” This work was conducted in Dr. Christopher Chen’s group in the Department of Bioengineering at the University of Pennsylvania. The research was supported by the National Institutes of Health and the American Heart Association.
Image 1: This is an immunofluorescence image of a human mesenchymal stem cell growing on a plate of microposts, which have the approximate consistency of Silly Putty. This image was taken after one day of culturing. The red dots are the microposts, which are relatively short in this sample. The green is the cell and the blue is its nucleus. This cell will differentiate into a bone cell. Credit: Michael T. Yang (University of Pennsylvania)
Image 2: This is an image taken with a scanning electron microscope of a human mesenchymal stem cell growing on a plate of long microposts approximately 13 microns in length. After one day of culturing, this cell exerts centripetal force, which can be seen in the bending of the microposts. This cell will differentiate into a fat cell. Credit: Jianping Fu (University of Michigan)
Image 3: This is an image taken with a scanning electron microscope of human mesenchymal stem cells growing on a plate of short microposts. After one day of culturing, these cells spread more than cells cultured on long microposts. These will differentiate into bone cells. Even though these cells bend their shorter microposts less than their counterparts growing on longer microposts, they exert greater force to do so. Credit: Jianping Fu (University of Michigan)
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