Described in the May 15 issue of Development, the finding improves understanding of how cells become specialized for secretion, which is a critical ability of certain glands and cell types in organisms from insects to humans.
The researchers discovered that a protein called CrebA single-handedly controls the entire set of events leading to secretion in the fruit fly's salivary gland and epidermis, its skin-like outer layer.
CrebA, or a closely related human gene, might play the same role in certain human cells, too, the researchers say.
In juvenile (type I) diabetes, for example, pancreatic cells that normally produce and secrete insulin don't work, and stem cells might be able to help fix that problem, the researchers note. "The key is knowing how pancreatic cells know what hormones to produce and release, or how any gland does, and the new findings add to that knowledge," says Deborah Andrew, Ph.D., professor of cell biology in Johns Hopkins' Institute for Basic Biomedical Sciences.
Curiosity brought Andrew and Elliott Abrams, then a graduate student, to focus on secretion in the salivary gland, the largest glandular organ in the fruit fly embryo, approximately six years ago. In humans and in fruit flies, the gland secretes saliva, a fluid containing water, mucus, electrolytes, and food-dissolving enzymes, into the mouth, and is important to the digestive system.
In their new experiments, the researchers looked at the expression of 34 secretory genes in a normal fruit fly embryo to see which genes were turned on when. All 34 genes were expressed at high levels in the early salivary gland, they found. According to Andrew, "This suggests the salivary gland becomes programmed for secretion because all the components required to allow secretion to occur are 'turned on'
Source:Johns Hopkins Medical Institutions