Transcript levels of the human serine/ threonine kinase h-sgk have been fou
nd to be highest in pancreas. In the present study, localization and regula
tion of h-sgk transcription in pancreatic tissue were elucidated. As was ap
parent from radioactive in situ hybridization, most pancreatic acinar cells
expressed high levels of h-sgk mRNA. h-sgk mRNA-positive cells were also f
ound in ductal epithelia but not in pancreatic islets. In biopsy specimens
from patients with pancreatitis, h-sgk mRNA levels were decreased in acinar
cells but abundant in numerous mononuclear interstitial cells within areas
of pancreatic necrosis and fibrosis. As shown by Northern blotting, h-sgk
transcription in DAN-G pancreatic tumor cells is upregulated by osmotic cel
l shrinkage, serum, phorbol esters (phorbol 12,13-didecanoate), and Ca2+ io
nophore A-23187 and decreased by staurosporine and cAMP. In conclusion, h-s
gk transcription is regulated not only by cell volume but also by serum, pr
otein kinase C stimulation, cAMP, and increase of intracellular Ca2+ activi
ty. The kinase may participate not only in normal function of exocrine panc
reas but also in fibrosing pancreatitis.