F. Bernardperrone et al., PANCREATIC TRYPSINOGEN I EXPRESSION DURING CELL-GROWTH AND DIFFERENTIATION OF 2 HUMAN COLON-CARCINOMA CELLS, American journal of physiology: Gastrointestinal and liver physiology, 37(6), 1998, pp. 1077-1086
Pancreatic trypsin has been found to induce tight junction or dome for
mation in some colon cancer cell lines (HT-29, Caco-2), and a tumor-as
sociated trypsinogen, trypsinogen type II, has been isolated from anot
her colon cancer cell line (COLO 205). We have tried to determine if t
rypsinogen is present and how its expression varies during cell cultur
e in KT-29 Glc+/- and Caco-2 cells, which exhibit enterocytic differen
tiation, and in HT-29 Glc+ cells, which never differentiate. Trypsinog
en mRNA presence and expression were demonstrated in these cells by mR
NA hybridization, RT-PCR, cytoimmunofluorescence, Western immunoblot a
nalysis, and gel filtration. Trypsinogen was found to be trypsinogen t
ype I and was mainly in zymogen form in culture media. Differentiating
cells exhibited variations in trypsinogen I expression, but cells tha
t remained undifferentiated did not. In the differentiated cells, a hi
gh and transient peak in trypsinogen I expression was observed during
the first steps of differentiation.