BOSTON, Mass. (November 21, 2010)—As debilitating as disease can be, sometimes it acts as a teacher.
Researchers at Harvard Medical School and the Harvard School of Dental Medicine have found that by mimicking a rare genetic disorder in a dish, they can rewind the internal clock of a mature cell and drive it back into an adult stem-cell stage. This new "stem cell" can then branch out into a variety of differentiated cell types, both in culture and in animal models.
"This certainly has implications for personalized medicine, especially in the area of tissue engineering," says Bjorn Olsen, the Hersey Professor of Cell Biology at Harvard Medical School and Dean of Research at the Harvard School of Dental Medicine.
These findings appear November 21, online in Nature Medicine.
Fibrodysplasia Ossificans Progressiva (FOP), which affect fewer than 1,000 people worldwide, is a horrific genetic disease in which acute inflammation causes soft tissue to morph into cartilage and bone. Over the course of a few decades, patients gradually become thoroughly ossified, as though parts of their body have turned to stone. There is no cure or treatment.
Damian Medici, an instructor of medicine at Harvard Medical School and Beth Israel Deaconess Medical Center, found that, unlike normal skeletal tissue, the pathological cartilage and bone cells from these patients contained biomarkers specific for endothelial cells—cells that line the interior of blood vessels. This led him to question whether or not the cartilage and bone growing in soft tissues of FOP patients had an endothelial origin.
Medici and his colleagues transferred the mutated gene that causes FOP into normal endothelial cells. Unexpectedly, the endothelial cells converted into a cell type nearly identical to what are called mesenchymal stem cells, or adult stem cells that can differentiate into bone, cartilage, muscle, fat, and even nerve cells. (Embryonic stem cells have the potential to become any type of cell, whereas adult stem cells are limited.)
What's more, through further experiments the researchers found that instead of using the mutated gene to induce the transformation, they could incubate endothelial cells with either one of two specific proteins (growth factors TGF-beta2 and BMP4) whose cellular interactions mimicked the effects of the mutated gene, providing a more efficient way to reprogram the cells.
Afterwards, Medici was able to take these reprogrammed cells and, in both culture dishes and animal models, coax them into developing into a group of related tissue types.
"It's important to clarify that these new cells are not exactly the same as mesenchymal stem cells from bone marrow," says Medici. "There are some important differences. However, they appear to have all the potential and plasticity of mesenchymal stem cells."
"The power of this system is that we are simply repeating and honing a process that occurs in nature," says Olsen. "In that sense, it's less artificial than other current methods for reprogramming cells."
According to study collaborator Frederick Kaplan, Isaac & Rose Nassau Professor of Orthopaedic Molecular Medicine at the University of Pennsylvania School of Medicine and a world expert on FOP, "While we want to use this knowledge to stop the renegade bone formation of FOP, these new findings provide the first glimpse of how to recruit and harness the process to build extra bone for those who desperately need it."
Medici and Olsen echo this, stating that the most direct application for these findings is the field of tissue engineering and personalized medicine. It is conceivable that transplant patients may one day have some of their own endothelial cells extracted, reprogrammed, and then grown into the desired tissue type for implantation. Host rejection would not be an issue.
This research was funded by the National Institutes of Health.
Nature Medicine, early online publication, Nov 21, 2010
"Conversion of vascular endothelial cells into multipotent stem-like cells"
Damian Medici(1), Eileen M Shore(2), Vitali Y Lounev(2,4), Frederick S Kaplan(2,4,5), Raghu Kalluri(1,6,7) & Bjorn R Olsen(8)
1-Division of Matrix Biology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
2-Deparment of Orthopaedic Surgery, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
3Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
4-Center for Research in Fibrodysplasia Ossificans Progressiva and Related Disorders, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
5-Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
6-Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
7Harvard–Massachusetts Institute of Technology Division of Health Sciences and Technology, Boston, Massachusetts, USA.
8-Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Harvard Medical School <http://hms.harvard.edu> has more than 7,500 full-time faculty working in 11 academic departments located at the School's Boston campus or in one of 47 hospital-based clinical departments at 17 Harvard-affiliated teaching hospitals and research institutes. Those affiliates include Beth Israel Deaconess Medical Center, Brigham and Women's Hospital, Cambridge Health Alliance, Children's Hospital Boston, Dana-Farber Cancer Institute, Forsyth Institute, Harvard Pilgrim Health Care, Hebrew SeniorLife, Joslin Diabetes Center, Judge Baker Children's Center, Massachusetts Eye and Ear Infirmary, Massachusetts General Hospital, McLean Hospital, Mount Auburn Hospital, Schepens Eye Research Institute, Spaulding Rehabilitation Hospital, and VA Boston Healthcare System.