Researchers at Wake Forest Baptist Medical Center and colleagues have identified a special population of adult stem cells in bone marrow that have the natural ability to migrate to the intestine and produce intestinal cells, suggesting their potential to restore healthy tissue in patients with inflammatory bowel disease (IBD).
Up to 1 million Americans have IBD, which is characterized by frequent diarrhea and abdominal pain. IBD actually refers to two conditions -- ulcerative colitis and Crohn's disease -- in which the intestines become red and swollen and develop ulcers, probably as the result of the body having an immune response to its own tissue.
While there is currently no cure for IBD, there are drug therapies aimed at reducing inflammation and preventing the immune response. Because these therapies aren't always effective, scientists hope to use stem cells to develop an injectable cell therapy to treat IBD.
The research findings are reported online in the FASEB Journal (the journal of the Federation of American Societies for Experimental Biology) by senior researcher Graca Almeida-Porada, M.D., Ph.D., professor of regenerative medicine at Wake Forest Baptist's Institute for Regenerative Medicine, and colleagues.
The new research complements a 2012 report by Almeida-Porada's team that identified stem cells in cord blood that are involved in blood vessel formation and also have the ability to migrate to the intestine.
"We've identified two populations of human cells that migrate to the intestine -- one involved in blood vessel formation and the other that can replenish intestinal cells and modulates inflammation," said Almeida-Porada. "Our hope is that a mixture of these cells could be used as an injectable therapy to treat IBD."
The cells would theoretically induce tissue recovery by contributing to a pool of cells within the intestine. The lining of the intestine has one of the highest cellular turnover rates in the body, with all cell types being renewed weekly from this pool of cells, located in an area of the intestine known as the crypt.
In the current study, the team used cell markers to identify a population of stem cells in human bone marrow with the highest potential to migrate to the intestine and thrive. The cells express high levels of a receptor (ephrin type B) that is involved in tissue repair and wound closure.
The cells also known to modulate inflammation were injected into fetal sheep at 55 to 62 days gestation. At 75 days post-gestation, the researchers found that most of the transplanted cells were positioned in the crypt area, replenishing the stem cells in the intestine.
"Previous studies in animals have shown that the transplantation of bone-marrow-derived cells can contribute to the regeneration of the gastrointestinal tract in IBD," said Almeida-Porada. "However, only small numbers of cells were successfully transplanted using this method. Our goal with the current study was to identify populations of cells that naturally migrate to the intestine and have the intrinsic ability to restore tissue health."
Almeida-Porada said that while the two studies show that the cells can migrate to and survive in a healthy intestine, the next step will be to determine whether they can survive in an inflamed intestine.
The research was supported by the National Heart, Lung, and Blood Institute under award number NHL097623 and HL073737 and grant P20 RR-016464 from the Idea Network of Biological Research Excellence Program of the National Center for Research Resources.
Co-authors were Saloomeh Mokhtari, Christopher D. Porada, and Melisa Soland, Wake Forest Baptist; and Evan Colletti, Craig Osborne, Karen Schlauch, Deena El Shabrawy, Takashi Yamagami, and Esmail D. Zanjani, University of Nevada. The two projects were performed while Almeida-Porada was at the University of Nevada prior to joining Wake Forest Baptist.
- E. Colletti, D. El Shabrawy, M. Soland, T. Yamagami, S. Mokhtari, C. Osborne, K. Schlauch, E. D. Zanjani, C. D. Porada, G. Almeida-Porada. EphB2 isolates a human marrow stromal cell subpopulation with enhanced ability to contribute to the resident intestinal cellular pool. The FASEB Journal, 2013; DOI: 10.1096/fj.12-205054
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