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Cellular localization, binding sites, and pharmacologic effects of TFF3 in experimental colitis in mice.

Abstract
Trefoil factors (TFFs) are essential for protection and restitution of the gastrointestinal mucosa but many aspects of TFF biology are unclear. Our aim was to compare the localization of endogenous TFFs and binding sites for injected TFF3 in the colon of healthy and colitic mice and to study the effect of TFF3 on dextrane sulfate sodium (DSS)-induced colitis in mice. Expression of endogenous TFF1-3 was examined by in situ hybridization and immunohistochemistry, and the distribution of intravenously, intraperitoneally, and subcutaneously administered (125)I-TFF3 by autoradiography and gamma-counting. The effect of systemically administered TFF3 on DSS-induced colitis was assessed. We found increased expression of endogenous TFF3 and increased binding of injected (125)I-TFF3 in the colon of animals with DSS-induced colitis. The distribution of intraperitoneally and subcutaneously administered (125)I-TFF3 was comparable. Systemic administration of the peptides reduced the severity of colitis. Expression of endogenous TFF3 and binding of systemically administered TFF3 are increased in DSS-induced colitis. Systemic administration of TFF3 attenuates the disease. These findings suggest a role of TFF3 in mucosal protection.
AuthorsStine Kjellev, Lars Thim, Charles Pyke, Steen S Poulsen
JournalDigestive diseases and sciences (Dig Dis Sci) Vol. 52 Issue 4 Pg. 1050-9 (Apr 2007) ISSN: 0163-2116 [Print] United States
PMID17342398 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Iodine Radioisotopes
  • Mucins
  • Peptides
  • TFF3 protein, human
  • Tff3 protein, mouse
  • Trefoil Factor-3
  • Dextran Sulfate
Topics
  • Animals
  • Autoradiography
  • Binding Sites
  • Colitis (chemically induced, metabolism, pathology)
  • Colon (metabolism, pathology)
  • Dextran Sulfate
  • Female
  • Goblet Cells
  • Immunohistochemistry
  • Injections, Intraperitoneal
  • Injections, Intravenous
  • Injections, Subcutaneous
  • Iodine Radioisotopes
  • Mice
  • Mice, Inbred BALB C
  • Mucins (administration & dosage, metabolism, pharmacokinetics, pharmacology)
  • Peptides (pharmacokinetics, pharmacology)
  • Tissue Distribution
  • Trefoil Factor-3

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