Abstract | BACKGROUND & AIMS: METHODS: RESULTS: Small bowel length and mass were greater in IGF-I transgenic mice than in wild-type mice. Villus height, crypt depth, and crypt cell mitoses were greater in jejunum of transgenics than wild-type mice, but jejunal disacharidase activities were not increased. The transgene was expressed strongly in villus epithelial cells. Insulin-like growth factor-binding protein 3 messenger RNA was localized in the lamina propria. Regional expression of both correlated with the increase in mucosal mass. CONCLUSIONS: Effects of IGF-I overexpression on intestinal length and mucosal mass were similar to effects of growth hormone overexpression observed previously. Excess of IGF-I increased crypt cell proliferation, whereas excess of growth hormone did not increase crypt cell proliferation. IGF-I excess stimulated differentiation of intestinal epithelial cells less effectively than growth hormone excess.
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Authors | K Ohneda, M H Ulshen, C R Fuller, A J D'Ercole, P K Lund |
Journal | Gastroenterology
(Gastroenterology)
Vol. 112
Issue 2
Pg. 444-54
(Feb 1997)
ISSN: 0016-5085 [Print] United States |
PMID | 9024298
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Insulin-Like Growth Factor Binding Protein 3
- RNA, Messenger
- Insulin-Like Growth Factor I
- Growth Hormone
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Topics |
- Animals
- Body Weight
- Cattle
- Energy Intake
- Gene Expression
- Growth Hormone
(genetics)
- Humans
- Insulin-Like Growth Factor Binding Protein 3
(genetics)
- Insulin-Like Growth Factor I
(genetics, metabolism)
- Intestinal Mucosa
(growth & development, physiology)
- Intestine, Small
(anatomy & histology, cytology, growth & development)
- Jejunum
(metabolism)
- Mice
- Mice, Transgenic
(genetics, metabolism, physiology)
- Mitosis
- Organ Size
- RNA, Messenger
(metabolism)
- Reference Values
- Tissue Distribution
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