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But the last decades have uncovered additional sites and cell types that also express the CCK gene at peptide level (Table 1). In some of these sites, proCCK is not processed to the known α-amidated peptides. But since CCK receptors also have such widespread expression (66, 67, 70–73, 94, 95), there is both room and need for delineation of the roles of CCK released from the “new” sites. Also mentioned before (9), “CCK in circulation originates mainly from intestinal endocrine cells. The release to blood was not possible to examine until specific assays were developed (10–12, 54).
GAME PROVIDERS
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For the SR146131–CCK1R–Gs–Nb35 complex, auto-picking-yielded 5,213,984 particle projections were subjected to 3D classification to discard particles in poorly defined classes, producing 898,915 particle projections. The re-picked particles were extracted and subjected to two rounds of 3D classification with four classes; the best-resolved class was selected each time. The resulting set of 606,684 particles was subjected to CTF refinement, Bayesian polishing and 3D auto refinement using the pixel size of 1.014 Å. The final map has an indicated global resolution of 3.0 Å at an FSC of 0.143. For the CCK-8–CCK1R–Gs–Nb35 complex, auto-picking-yielded 5,768,688 particle projections were subjected to 3D classification to discard particles in poorly defined classes, producing 1,608,563 particle projections.
CCK peptides release insulin and glucagon more potently in man and pig than in dog and rat (51, 85–87). The difference is partly due to neurons in pancreatic islets that release CCK-8 and CCK-5 in man and pig (51), whereas rat and dog islets have no such innervation (50, 51). Moreover, islet cells in man and pig also express the CCK2 receptor abundantly (73), whereas rat islet cells express mainly the CCK1 receptor (88). While the interest in the effect of CCK on the exocrine pancreas was for many years restricted to enzyme secretion, it is now well established that CCK also stimulates fluid and bicarbonate secretion.