The organs in our bodies house stem cells that are necessary to regenerate cells when they become damaged, diseased or too old to function. Researchers at Rutgers University have identified a new factor that is essential for maintaining the stem cells in the brain and gut and whose loss may contribute to anxiety and cognitive disorders and to gastrointestinal diseases.
The study, published in the journal Stem Cell Reports, reveals the importance of the insulin-like growth factor II gene in adult stem cell maintenance in these two organs. The gene provides key support for the existence of two, functionally distinct sets of stem cells in the intestine, whose unregulated self-renewal and proliferation may contribute to colorectal cancers.
The role that the insulin-like growth factor II gene plays in adult stem cells has been largely unknown. This growth factor was previously regarded as dispensable in adults. The discovery that there is a factor — this gene product — that is common between more than one adult stem cell population is remarkable.”
The findings indicate that this growth factor is essential for multiple types of adult stem cells, including those critical for cognitive function, sense of smell and for renewing the lining of the small intestine in adults.
In the study, the researchers removed the gene from adult mice either rapidly over five days or more slowly over 15 days. In the intestine, the fast deletion of the gene led to a rapid loss of fast-cycling stem cells that replenish the gut lining, leading to dramatic weight loss and death within a week. A slower deletion of the gene allowed the mice to survive due to the recruitment of a second, and more inactive, population of gut stem cells, whose existence has been debated. Additionally, the study revealed that half of the stem cells in two regions of the brain that house neural stem cells were lost, causing deficits in learning and memory, increased anxiety and a loss of the sense of smell.
When the gene was removed acutely, the stem cells in glands in the inner surface of the small intestine could not continue their normal cycle of continued cell replacement, causing organ failure. However, when the gene was deleted slowly, it gave the other stem cells an opportunity to take over for the lost stem cells.”