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Stem-cell Transplantation Improves Muscles In Muscular Dystrophy Animal Model, Researchers Report

Date:
January 22, 2008
Source:
UT Southwestern Medical Center
Summary:
Using embryonic stem cells from mice, researchers have prompted the growth of healthy -- and more importantly, functioning -- muscle cells in mice afflicted with a human model of Duchenne muscular dystrophy.
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Using embryonic stem cells from mice, UT Southwestern Medical Center researchers have prompted the growth of healthy -- and more importantly, functioning -- muscle cells in mice afflicted with a human model of Duchenne muscular dystrophy.

The study represents the first time transplanted embryonic stem cells have been shown to restore function to defective muscles in a model of muscular dystrophy.

The researchers' newly developed technique, which involves stringent sorting to preserve all stem cells destined to become muscle, avoids the risk of tumor formation while improving the overall muscle strength and coordination of the mice, the researchers found.

The mice used in the study lacked dystrophin, the same protein that humans with the fatal wasting disease also are missing.

The study is headed by Dr. Rita Perlingeiro, assistant professor of developmental biology and molecular biology."We envision eventually developing a stem-cell therapy for humans with muscular dystrophy, if we are able to successfully combine this approach with the technology now available to make human embryonic stem cells from reprogrammed skin cells," Dr. Perlingeiro said. "These cells can be transplanted into the muscle, and they cause muscle regeneration resulting in stronger contractility."

The study represents a major step in the field, she said, because the researchers were able to tease out exactly the cells they wanted.

"The problem had been that embryonic stem cells make everything," Dr. Perlingeiro said. "They make a great variety of cells. The trick is to pull out only the one type you want."

The UT Southwestern researchers focused on manipulating genes that are active in the very early stages as embryonic stem cells start to develop into more specialized cells. At first, they activated a gene called Pax3, which is involved in creating muscle cells, and then injected those cells into the animals' muscles. Those cells caused tumors containing many different types of cells, indicating that there were still residual undifferentiated embryonic stem cells in the cultures at the time of implantation.

"Even if there are 10 undesirable cells, that's too many," Dr. Perlingeiro said.

The researchers then began using fluorescent dyes to sort cells depending on whether some surface markers were turned on while others were turned off. By analogy, it was as if they were dealing with a crowd of people and wanted to pull out only those with red hair, green scarves and blue coats, while those with red hair, green scarves and no coats would be disqualified.

The final selection of cells, containing only one type, was again injected into the animals' hind-limb muscles. After a month, the fluorescent dyes showed that the cells had deeply penetrated the muscle, an indication that they were growing and reproducing as desired, and many of the muscle fibers also contained dystrophin, the key protein lacking in muscular dystrophy.

After three months, the mice also showed no signs of tumors.

Tests of isolated muscles showed that the treated muscles were significantly stronger than untreated mice lacking dystrophin, although not quite as strong as those of normal mice.

The treated mice also were tested for coordination. Again, their performance was better than that of untreated mice, but not as good as that of normal mice.

"The improved coordination is significant because it shows the embryonic stem cells have benefited the animal's quality of life, not simply caused an isolated growth with no overall improvement," Dr. Perlingeiro said.

The researchers will next investigate whether these transplanted cells can make "muscle stem cells," which are partially developed cells in muscle tissue that serve as a reserve to replenish muscles. They also are testing their implantation approach in animal models of other types of muscular dystrophy.

The research article is available online January 20 and in the February issue of Nature Medicine. Other UT Southwestern researchers involved in the study were lead author Dr. Radbod Darabi, postdoctoral researcher in developmental biology; allied health student Kimberly Gehlbach; Dr. Robert Bachoo, assistant professor of neurology and internal medicine; Shwetha Kamath, research assistant in developmental biology; Dr. Mitsujiro Osawa, postdoctoral fellow in developmental biology; Dr. Kristine Kamm, professor of physiology; and Dr. Michael Kyba, assistant professor of developmental biology and molecular biology.

The work was supported by the Dr. Bob and Jean Smith Foundation.


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Materials provided by UT Southwestern Medical Center. Note: Content may be edited for style and length.


Cite This Page:

UT Southwestern Medical Center. "Stem-cell Transplantation Improves Muscles In Muscular Dystrophy Animal Model, Researchers Report." ScienceDaily. ScienceDaily, 22 January 2008. <www.sciencedaily.com/releases/2008/01/080120160709.htm>.
UT Southwestern Medical Center. (2008, January 22). Stem-cell Transplantation Improves Muscles In Muscular Dystrophy Animal Model, Researchers Report. ScienceDaily. Retrieved October 8, 2024 from www.sciencedaily.com/releases/2008/01/080120160709.htm
UT Southwestern Medical Center. "Stem-cell Transplantation Improves Muscles In Muscular Dystrophy Animal Model, Researchers Report." ScienceDaily. www.sciencedaily.com/releases/2008/01/080120160709.htm (accessed October 8, 2024).

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