Prohormone convertase 2 is necessary for the formation of cholecystokinin-22, but not cholecystokinin-8, in RIN5F and STC-1 cells

Endocrinology. 1997 Sep;138(9):3620-3. doi: 10.1210/endo.138.9.5399.

Abstract

Two endocrine tumor cell lines from pancreas (RIN5F) and intestine (STC-1) express cholecystokinin (CCK) messenger RNA and are able to posttranslationally process pro-CCK to CCK-22 and CCK-8 amide. Both of these forms are also secreted by these cells. Because they make and secrete forms of amidated CCK larger than CCK-8, they represent a model of pro-CCK processing in the gut and allow investigation of possible mechanisms for tissue differences in prohormone processing. Both of these cells express two endoproteases convertase-1 (PC1) also known as PC3 and prohormone convertase-2 (PC2), which may be involved in pro-CCK processing. We have previously shown than inhibition of PC1 expression in these cells using stable expression of antisense messenger RNA caused a significant reduction in cellular content of amidated CCK and caused a selective depletion of CCK-8 with a comparative sparing of CCK-22. We demonstrate here that inhibition of PC2 expression in these cells also caused a large initial decrease in CCK content and produced a selective depletion of CCK-22 and a comparative sparing of CCK-8. These results support both a role for both PC1 and PC2 in pro-CCK processing in these cells and the hypothesis that tissue-specific processing of pro-CCK may be explained by differences in expression or activity of PC1 and PC2.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cholecystokinin / biosynthesis*
  • Cholecystokinin / genetics
  • Gene Expression
  • Intestinal Neoplasms / enzymology
  • Pancreatic Neoplasms / enzymology
  • Peptide Fragments / biosynthesis*
  • Peptide Fragments / genetics
  • Proprotein Convertase 2
  • RNA, Antisense / genetics
  • RNA, Messenger / genetics
  • Sincalide / biosynthesis*
  • Sincalide / genetics
  • Subtilisins / genetics
  • Subtilisins / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Peptide Fragments
  • RNA, Antisense
  • RNA, Messenger
  • Cholecystokinin
  • cholecystokinin 22 C-terminal fragment
  • Subtilisins
  • Proprotein Convertase 2
  • Sincalide