The researchers found that two independent groups of cells generate the same signal by different pathways and that these cells subsequently act together to send the signal to the target cell. In this manner, the receptor cell receives the signal from two distinct sources. The results of this study appear in today’s advanced electronic issue of the journal, PNAS.
Jordi Casanova (IRB Barcelona/CSIC) explains that different types of cells working together to send a message can be regarded as a “security measure designed to ensure that the signal reaches the receptor cell in the proper fashion, neither too weakly nor too strongly”. Using RNA interference techniques (RNAi), the researchers observed that it was necessary to disactivate the signal in both groups of cells in order to prevent the message from being sent. They also observed that overstimulating signal production (producing more of the signalling molecule) created problems in the receptor cell, causing it to develop incorrectly.
Researchers made the discovery by studying the behaviour of a gene called torso-like during the early stages of embryonic development of the Drosophila fly. Two groups of cells activated the same torso-like gene separately and by different mechanisms when they were still in separate compartments inside the Drosophila ovary. Subsequently, the cells migrated until they met and jointly signalled the target cell.
Marc Furriols, lead author of the study, explains that the torso-like gene activates a membrane receptor molecule that is specific to Drosophila, but that the molecule belongs to a receptor family (that includes, for example, the human growth factor), which also reacts when it receives an external signal. “This research describes a very signalling mechanism in the fly which is very basic. It gives us good insight into how these mechanisms work so that we can later manipulate and control them.
Many of these pathways and signalling systems have been observed throughout evolution and hence, studies with models such as the fruit fly, can provide further insight into how these signalling mechanisms work in humans.
Sonia Armengou | alfa
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