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GH/STAT5 signaling during the growth period in livers of mice overexpressing GH.
- Source :
-
Journal of molecular endocrinology [J Mol Endocrinol] 2015 Apr; Vol. 54 (2), pp. 171-84. Date of Electronic Publication: 2015 Feb 17. - Publication Year :
- 2015
-
Abstract
- GH/STAT5 signaling is desensitized in the liver in adult transgenic mice overexpressing GH; however, these animals present greater body size. To assess whether the STAT5 pathway is active during the growth period in the liver in these animals, and how signaling modulators participate in this process, growing transgenic mice and normal siblings were evaluated. STAT5 does not respond to an acute GH-stimulus, but displays higher basal phosphorylation in the livers of growing GH-overexpressing mice. GH receptor and the positive modulators glucocorticoid receptor and HNF1 display greater abundance in transgenic animals, supporting the activity of STAT5. The negative modulators cytokine-induced suppressor and PTP1B are increased in GH-overexpressing mice. The suppressors SOCS2 and SOCS3 exhibit higher mRNA levels in transgenic mice but lower protein content, indicating that they are being actively degraded. Therefore, STAT5 signaling is increased in the liver in GH-transgenic mice during the growth period, with a balance between positive and negative effectors resulting in accelerated but controlled growth.<br /> (© 2015 Society for Endocrinology.)
- Subjects :
- Animals
Gene Expression Regulation, Developmental
Insulin-Like Growth Factor I metabolism
Mice, Inbred C57BL
Mice, Transgenic
Phosphorylation
Receptors, Somatotropin genetics
Receptors, Somatotropin metabolism
Suppressor of Cytokine Signaling Proteins genetics
Suppressor of Cytokine Signaling Proteins metabolism
Growth Hormone metabolism
Liver growth & development
Liver metabolism
STAT5 Transcription Factor metabolism
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 1479-6813
- Volume :
- 54
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of molecular endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 25691498
- Full Text :
- https://doi.org/10.1530/JME-14-0262