Lost stem cells naturally replaced by non-stem cells, fly research suggests.
The discovery sheds light on the tiny "environments" that stem cells occupy in animal bodies and may help explain how stem cells in tumors replenish themselves, the researchers report.
Damage of the kind duplicated in the laboratory occurs naturally after exposure to radiation and perhaps also after ingestion of toxic chemicals such as those used in chemotherapy.
The research group, led by Erika Matunis, a professor of cell biology at the Johns Hopkins University School of Medicine, has been using the fruit fly as a model living system in which to study stem cells in their natural state.
Most stem cell research is done on cells grown in the laboratory, but in real life, stem cells reside in tissues, where they are sequestered in tiny spaces known as niches.
Adult stem cells keep dividing throughout life to make various kinds of cells, like new blood cells and germ cells.
Matunis's group studies such niches in fruit fly testes, the sperm-producing organs shaped like a coiled tube whose end houses a niche. In the niche are three kinds of cells: germ line stem cells, which divide to produce sperm; somatic cyst stem cells, which make a kind of cell that helps the sperm-producing cells out; and hub cells, which make signals that keep the other two kinds of cells going.
The hub cells are not stem cells; they have settled on their final form, incapable of dividing further or changing their function, or so everyone thought.
However, in trying to figure out what happens when the somatic cyst stem cells are killed off, Matunis suggested that a graduate student figure out how to best do away with them, thinking the task would be straight-forward.
Instead, it took a lot of patient combinations of different genes working together to kill the somatic cyst cells.
When they finally figured out a way to kill all of the somatic stem cells, they thought that the rest of the tissue would probably just empty out.
In 35 percent of testes, that's what happened. But in the rest, the somatic stem cells grew back. This was a surprise, and left a puzzle: Where were the new somatic stem cells coming from?
The answer, it turned out, was the hub cells. When the somatic stem cells were destroyed, the hub cells cranked up their machinery for cell division. The team did several experiments to be sure that the hub cells were involved, including one in which they genetically marked the hub cells and saw the mark appear in the newly formed somatic stem cells, a clear sign that hub cells had divided to make new stem cells.
The new stem cells created by the hub cells aren't exactly the same as the old ones.
They thought some of them looked a little bit weird. Sometimes, the new cells made molecules that only hub cells normally make. As the researchers looked closer, they realized that the damaged and recovered testes were making new niches. Instead of just one pocket of stem cells, a damaged testis might have two or three.
They don't know how the new niches are formed, but speculate that the original niche gets bigger as the new cells divide, then splits.
The group is doing more experiments aimed at "explaining the basics of how niches work in general," Matunis said.
The research may be useful for understanding cancer, because a lot of cancer involves cancer stem cells, also known as tumor-initiating cells. Many tumors seem to have stem cells inside them that divide to keep the tumor going. Knowing how tumor niches support the continued growth and division of stem cells might one day offer new targets for controlling such growth.
In the study, the damage was caused deliberately, but the research suggests one way that natural damage might scatter stem cells around the body.
The researchers hope to unravel the signals that are changing when we damage this niche.
Citation: "Conversion of Quiescent Niche Cells to Somatic Stem Cells Causes Ectopic Niche Formation in the Drosophila Testis"; Phylis Hetie et al.; Cell Reports, 2014; DOI: 10.1016/j.celrep.2014.03.058
Contact: Erika Matunis, email@example.com
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|Title Annotation:||Basic Research|
|Publication:||Stem Cell Research News|
|Date:||Apr 28, 2014|
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