Regulation of pancreatitis-associated protein (HIP/PAP) mRNA levels in mouse pancreas and small intestine

Clin Sci (Lond). 1996 Aug;91(2):213-8. doi: 10.1042/cs0910213.

Abstract

1. In the present study we have examined the expression of pancreatitis-associated protein mRNA in mouse pancreas and small intestine and determined the effect of a number of factors on the steady-state level of the RNA. 2. The normally low level of pancreatitis-associated protein mRNA in pancreas increased severalfold after 6 h of hypoxia, reaching peak levels (approximately 10-fold greater than normal) after 24 h hypoxia. After 3 days' hypoxia pancreatitis-associated protein mRNA levels were again undetectable. 3. In the pancreas the level of pancreatitis-associated protein mRNA was also increased by alcohol and iron overload, but not by paracetamol. 4. In the small intestine expression of pancreatitis-associated protein mRNA was higher in normal ileum than in duodenum. In the ileum pancreatitis-associated protein mRNA levels were increased 7 to 15-fold after 6 h hypoxia, reaching peak levels by 24 h. Levels declined after 3 days' hypoxia, but remained higher than normal. 5. In the ileum long-term (4 weeks) dietary iron deficiency reduced pancreatitis-associated protein mRNA levels compared with control fed mice, whereas parenteral iron overload increased pancreatitis-associated protein mRNA levels. 6. The data presented suggest regulation of pancreatitis-associated protein gene expression by both oxygen tension and iron status.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / pharmacology
  • Acute-Phase Proteins / genetics
  • Acute-Phase Proteins / metabolism*
  • Analgesics, Non-Narcotic / pharmacology
  • Animals
  • Antigens, Neoplasm*
  • Biomarkers, Tumor*
  • Cell Line
  • Duodenum / drug effects
  • Duodenum / metabolism
  • Ethanol / pharmacology
  • Gene Expression Regulation*
  • Hypoxia / metabolism
  • Ileum / drug effects
  • Ileum / metabolism
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism*
  • Iron / pharmacology
  • Lectins, C-Type*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Pancreas / metabolism*
  • Pancreatitis-Associated Proteins
  • Proteins*
  • RNA, Messenger / metabolism*
  • Time Factors

Substances

  • Acute-Phase Proteins
  • Analgesics, Non-Narcotic
  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • Lectins, C-Type
  • Pancreatitis-Associated Proteins
  • Proteins
  • REG3A protein, human
  • RNA, Messenger
  • Reg3b protein, mouse
  • Acetaminophen
  • Ethanol
  • Iron