M. Jackerott et al., PYY IN DEVELOPING MURINE ISLET CELLS - COMPARISONS TO DEVELOPMENT OF ISLET HORMONES, NPY, AND BRDU INCORPORATION, The Journal of histochemistry and cytochemistry, 44(8), 1996, pp. 809-817
Exhaustive characterizations of antisera to the structurally related p
eptides pancreatic polypeptide (PP), neuropeptide Y (NPY), and peptide
YY (PYY) enabled us to establish the developmental pattern of these p
eptides in rat and mouse pancreas. PYY was the earliest detectable pep
tide and was present in all early appearing endocrine cell types, NPY
appeared later and occurred exclusively in a subpopulation of insulin
cells, whereas PP cells arose latest. At the earliest stage studied, a
ll endocrine cells stored PYY, Most of these cells also contained gluc
agon. Subsequently, the endocrine cells comprised glucagon + PYY cells
and glucagon + PYY + insulin cells, Later, cells storing either only
insulin or insulin + PYY appeared. Quantitations of the relative numbe
rs of these cell populations during development were consistent with a
precursor role of triple-positive (insulin + glucagon + PYY) tells, M
oreover, bromodeoxyuridine (BrdU) injections at E15.5 showed that a la
rge percentage of triple-positive cells were in S-phase and therefore
were actively dividing, whereas almost no pure insulin cells or insuli
n + PYY cells synthesized DNA at this time, These results suggest that
PYY-positive endocrine cells may represent precursors for mature isle
t cells.