November 4, 2004 -- Researchers have succeeded in growing sperm stem cells in laboratory cultures. These cells were then transferred to infertile mice who produced sperm and fathered baby mice. Each baby mouse was genetically related to the sperm stem cell donor, not to the mouse producing the sperm.
Actually, this research team has been working on similar technology for over ten years. What is new is that specific genes can be inserted into the sperm stem cells which can then be grown in culture to provide an endless supply of these cells.
The researchers point out that their technology developed in mice could also be used to treat infertility in humans. Sperm stem cells could be removed from a donor, cultured to increase their numbers, frozen, and then reimplanted back into the donor (or another male) at a future date.
The researchers also propose that these sperm stem cells have the "potential" of serving as a source for more versatile adult stem cells to replace diseased or injured tissue. Because of the current controversy swirling around the development of stem cell lines, this application requires a much bigger leap of faith.
Barbara K. Hecht,
Frederick Hecht, M.D.
Medical Editors, MedicineNet.com
Researchers Grow Sperm Stem Cells in Laboratory Cultures
Advance Could Lead To New Infertility Treatments, Source of Adult Stem Cells
A team of researchers working with cells from mice has overcome a technical barrier and succeeded in growing sperm progenitor cells in laboratory culture. The researchers transplanted the cells into infertile mice, which were then able to produce sperm and father offspring that were genetically related to the donor mice.
"This advance opens up an exciting range of possibilities for future research, from developing new treatments for male infertility to enhancing the survival of endangered species," said Duane Alexander, M.D., Director of the NICHD.
Their research, funded in part by the National Institute of Child Health and Human Development of the National Institutes of Health, will be published online this week in an upcoming issue of Proceedings of the National Academy of Sciences.
Led by Hiroshi Kubota, D.V.M., Ph.D., the team of researchers from the University of Pennsylvania School of Veterinary Medicine in Philadelphia, also included Mary Avarbock and Ralph L. Brinster V.M.D., Ph.D. The researchers succeeded in developing the culture medium containing the precise combination of cellular growth factors needed for the cells to reproduce themselves outside the body. Known as spermatogonial stem cells, the cells are incapable of fertilizing egg cells but give rise to cells that develop into sperm.
In 1994, this same research team developed the means to transplant spermatogonial stem cells from one mouse into another. The recipient mice then produced sperm - fully capable of fertilizing egg cells - with the genetic characteristics of the donor mice.
Because they can now grow spermatogonial stem cells in culture, researchers have a ready source of cells that they could manipulate genetically, explained the study's senior author, Ralph Brinster.
For example, researchers could implant a new gene into a spermatogonial cell, reproduce a large number of spermatogonial cells in the culture medium, and then implant the cells into recipient animals. These animals could then pass the new trait on to their offspring. The ability to introduce a new trait into animals would greatly assist breeders of both livestock and laboratory animals.
Moreover, by culturing and freezing spermatogonial stem cells from a valuable livestock animal or an endangered species, researchers could extend the reproductive life of that animal indefinitely. (The researchers developed a technique for successfully freezing and thawing spermatogonial cells in 1996.)
By manipulating the culture media that contains the spermatogonial stem cells, researchers might also be able to induce the spermatogonial cells to develop into sperm cells that could be used to fertilize eggs, providing a method to treat some types of infertility.
"This finding is likely to be applicable to humans," Dr. Brinster said. He added that the same growth factors needed to culture the mouse stem cells would likely foster the growth of human spermatogonial cells as well as the cells of other mammals.
Currently, males who undergo chemotherapy that renders them infertile can store their semen so that it can be used at a later date, should they wish to father children. However, this approach results in a less than 50 percent success rate. Boys who are too young to provide a semen sample but who also need such chemotherapy treatments could also be helped by the new technique. Their spermatogonial stem cells could be cultured to increase their numbers, frozen, and reimplanted at a later date, restoring their fertility.
Moreover, the new culture technique would allow researchers to further investigate the potential of spermatogonial stem cells as a source for more versatile adult stem cells to replace diseased or injured tissue. The replacement tissue might be used to help patients with spinal cord injury, or disorders like Parkinson's disease or heart disease.
To conduct their study, Dr. Kubota and his colleagues began with mice that had been genetically altered to express green fluorescent protein, or GFP, which gives off a green light in the presence of a certain wavelength of light. During key stages of the experiment, tissue from the donor mice gave off a green light.
At the first step, the researchers could distinguish spermatogonial stem cells from the cells used to nurture them in lab cultures by the green light the spermatogonial stem cells gave off. (A photograph of the spermatogonial stem cells appears at (http://www.nichd.nih.gov/new/releases/stem_cell.cfm.)
The spermatogonial stem cells also gave off green light when they grew and reproduced in the testes of the recipient mice. Similarly, about half of the baby mice fathered by the recipient mice also glowed green (See photo at http://www.nichd.nih.gov/new/releases/green_brown_mice.cfm.)
Additional funding for this research was provided by the Commonwealth and General Assembly of Pennsylvania, and the Robert J. Kleberg, Jr. and the Helen C. Kleberg Foundation.
Source: National Institutes of Health press release, Wednesday, November 3, 2004