Abstract | BACKGROUND: METHODS: We tested whether known decreases in arachidonate release in cells lacking Gi alpha2 would result in decreased PGE2 production and tissue PGE2 levels. PGE2 levels were significantly decreased in the colon of Gi alpha2-/- mice. RESULTS: Gi alpha2-/- myofibroblasts from the small intestine and colon both released asymptotically equal to 50% less arachidonate and 3- to 7-fold less PGE2 and 6-keto PGF1alpha in response to adenosine triphosphate, thrombin, tumor necrosis factor-alpha, or lipopolysaccharide, in a partially cyclooxygenase (COX)-2-dependent manner. Decreased arachidonate release did not appear to be caused by a defect in cPLA2 translocation in the absence of Gi alpha2. Basal myofibroblast COX-1 and COX-2 expression was downregulated in Gi alpha2-/- cells. No differences in proliferation rates were found between serum-starved or serum-activated wild-type (WT) and Gi alpha2-/- myofibroblasts. Finally, treatment of Gi alpha2-/- mice with the EP4-specific PGE2 receptor agonist ONO-AE1-329 significantly decreased the severity of established colitis. CONCLUSIONS: These findings confirm a requirement for Gi alpha2 in intestinal and colonic myofibroblast-derived prostanoid production and confirm the importance of mucosal PGE2 in the suppression of colitis.
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Authors | Robert Andrew Edwards, Andrew Zoller Smock |
Journal | Inflammatory bowel diseases
(Inflamm Bowel Dis)
Vol. 12
Issue 3
Pg. 153-65
(Mar 2006)
ISSN: 1078-0998 [Print] England |
PMID | 16534415
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Arachidonate 12-Lipoxygenase
- Cyclooxygenase 1
- Cyclooxygenase 2
- Dinoprostone
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Topics |
- Animals
- Arachidonate 12-Lipoxygenase
(deficiency)
- Base Sequence
- Cells, Cultured
- Colon
(cytology)
- Cyclooxygenase 1
(metabolism)
- Cyclooxygenase 2
(metabolism)
- Dinoprostone
(biosynthesis)
- Disease Models, Animal
- Down-Regulation
- Enzyme-Linked Immunosorbent Assay
- Inflammatory Bowel Diseases
(enzymology, pathology)
- Intestinal Mucosa
(enzymology, metabolism)
- Intestine, Small
(cytology)
- Mice
- Mice, Inbred Strains
- Molecular Sequence Data
- Reverse Transcriptase Polymerase Chain Reaction
- Sensitivity and Specificity
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