Growth hormone signaling in fibroblasts from newborn boys and prepubertal boys
Author
dc.contributor.author
Ocaranza Osses, Paula
Author
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Morales, Fernanda
Author
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Matamala, Álvaro
Author
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Gaete, Ximena
Author
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Román, Rossana
Author
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Lammoglia, Juan Javier
Author
dc.contributor.author
Cassorla Goluboff, Fernando
Admission date
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2016-12-02T18:53:01Z
Available date
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2016-12-02T18:53:01Z
Publication date
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2016-04
Cita de ítem
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Growth Hormone & IGF Research 27 (2016) 18–27
es_ES
Identifier
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1532-2238
Identifier
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10.1016/j.ghir.2016.01.003
Identifier
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https://repositorio.uchile.cl/handle/2250/141625
Abstract
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Background/aim: Responsiveness to GH in target cells is mediated by its receptor, which activates the Janus kinase-2 (JAK2) and STAT5 (signal transducers and activators of transcription 5) leading to the expression of IGF-1 and IGFALS. The aim of this study was to compare the GH signaling pathway in newborns and prepubertal boys.
Subjects and methods: We determined the GHR protein content and the effect of stimulation with recombinant human GH (rhGH; 200 ng/mL) on JAK2 and STAT5 phosphorylation in skin fibroblast cultures obtained from newborns and prepubertal boys. The transcript levels of IGFALS and IGF-I, were also studied and compared after 16 h or 24 h of stimulation with GH in both study groups.
Results: Newborn infants showed less GHR protein than the prepubertal boys. After rhGH stimulation, JAK2 and STAT5 phosphorylation was absent in skin fibroblasts from newborns, but was clearly detectable in prepubertal boys. After 16 h of treatment with rhGH, IGFALS and IGF-I transcript levels increased in the prepubertal boys when compared to baseline. In newborns, however, we did not observe a response after 16 and 24 h of rhGH stimulation.
Conclusion: The significant attenuation of the GH signaling pathway observed in fibroblasts from newborn boys appears to be related to a reduction in GHR content and lack of phosphorylation of JAK2 and STAT5 in response to rhGH. This might impair STAT5 dimer formation, leading to a reduction in the transcript levels of IGFALS and IGF-I during the newborn period.