Cytoplasmic and nuclear STAT3 in GH-stimulated fibroblasts of children with idiopathic short stature
Author
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Martínez Pinto, Jonathan
Author
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Salazar, Teresa
Author
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Ocaranza, Paula
Author
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Fuentes, Ariel
Author
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Román, Rossana
Author
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Cassorla Goluboff, Fernando
Admission date
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2019-03-11T13:00:21Z
Available date
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2019-03-11T13:00:21Z
Publication date
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2010
Cita de ítem
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Hormone Research in Paediatrics, Volumen 74, Issue 4, 2018, Pages 251-258
Identifier
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16632818
Identifier
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16632826
Identifier
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10.1159/000313415
Identifier
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https://repositorio.uchile.cl/handle/2250/165103
Abstract
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Background: STAT5, which plays an important role in GH signal transduction, has been studied extensively in children with growth retardation, but there is scarce information regarding STAT3. Aim: We determined total and phosphorylated STAT3 after GH stimulation in fibroblasts from children with idiopathic short stature (ISS) and control children with normal stature. Subjects and Methods: We studied 15 prepubertal children (age 7.6 ± 0.4 years) with short stature (height -2.8 ± 0.2 SDS), decreased growth velocity (<p10), a GH response of >10 ng/ml to the clonidine stimulation test and decreased serum IGF-I concentrations (<-1 SDS), and 19 control children with normal stature (age 6.7 ± 0.3 years). We determined the levels of total and phosphorylated STAT3 in the cytoplasmic and nuclear fractions of fibroblast cultures obtained from a skin biopsy, stimulated with GH (200 ng/ml) for 15-60 min. Results: We observed a reduction in nuclear pSTAT3 levels and a lower nuclear/cytoplasmic STAT3