In research published in the April 1 issue of Blood, Coller and Beau Mitchell, a research associate in Coller's lab, further characterize the ?IIb?3 receptor by exploring its production and degradation. With colleagues at the Mount Sinai School of Medicine, they found that the production of the receptor, the protein complex of both ?IIb and ?3, is dependent on a third molecule called calnexin. Calnexin plays an important role in protein folding, and the researchers found that it not only helps form the ?IIb?3 receptor complex, but also tags improperly folded ?3 proteins for destruction. Their findings suggest that the factor that controls receptor formation is likely the calnexin cycle; if the two receptor proteins fail to form a correctly folded complex, ?IIb is broken down by the cell. Coller hopes that further study of ?IIb?3 will yield more information about not just Glanzmann thrombasthenia but the synthesis of other receptors like it. These receptors, which are in the integrin superfamily, play a role in many different functions, including embryonic development, inflammation, and tumor growth and metastases, Coller says. "Insights into rare diseases allow us to study and devise strategies for common diseases."