L. Friishansen et Jf. Rehfeld, ILEAL EXPRESSION OF GASTRIN AND CHOLECYSTOKININ - IN SEARCH OF A RELATED HORMONE, FEBS letters, 343(2), 1994, pp. 115-119
Antibodies against the common active site of cholecystokinin (CCK) and
gastrin stain three endocrine celltypes in the gut: G-cells (that syn
thesize gastrin) I-cells (that synthesize CCK), and TG-cells (whose pr
oduct is unknown). In order to examine whether TG-cells either process
progastrin or proCCK in a specific manner, or express a novel gastrin
-CCK related hormone, we studied the distal porcine ileum, which have
far more TG- than G- and I-cells. Ileal CCK and gastrin mRNA correspon
ded to those of the antroduodenal mucosa. Gel, ion-exchange and revers
ed-phase chromatography monitored with sequence-specific immunoassays
showed that the ileal mucosa on average contain 0.3 and 7.6 pmol/g pro
gastrin and proCCK, respectively; 1.1 and 13.5 pmol/g glycine-extended
intermediates; and 1.1 and 24.8 pmol/g of bioactive carboxyamidated g
astrin and CCK, respectively. Gastrin was present only as non-sulfated
gastrin-34, whereas CCK occurred in forms similar to those of the pro
ximal intestine. Although ileal progastrin processing is tissue specif
ic, the amounts of gastrin and CCK are too small to explain the TG-cel
ls. Moreover, since the ileal extracts were without traces of other pe
ptides having the C-terminus common to gastrin and CCK, the results su
ggest that TG-cells produce a peptide, which is only weakly related to
gastrin and CCK.