Growth hormone-specific induction of the nuclear localization of porcine growth hormone receptor in porcine hepatocytes

The phenomenon of nuclear translocation of growth hormone receptor (GHR) in human, rat, and fish has been reported. To date, this phenomenon has not been described in a domestic animal (such as pig). In addition, the molecular mechanisms of GHR nuclear translocation have not been thoroughly elucidat...

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Veröffentlicht in:Domestic animal endocrinology 2017-10, Vol.61, p.39-47
Hauptverfasser: Lan, H.N., Hong, P., Li, R.N., Shan, A.S., Zheng, X.
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Sprache:eng
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Zusammenfassung:The phenomenon of nuclear translocation of growth hormone receptor (GHR) in human, rat, and fish has been reported. To date, this phenomenon has not been described in a domestic animal (such as pig). In addition, the molecular mechanisms of GHR nuclear translocation have not been thoroughly elucidated. To this end, porcine hepatocytes were isolated and used as a cell model. We observed that porcine growth hormone (pGH) can induce porcine GHR's nuclear localization in porcine hepatocytes. Subsequently, the dynamics of pGH-induced pGHR's nuclear localization were analyzed and demonstrated that pGHR's nuclear localization occurs in a time-dependent manner. Next, we explored the mechanism of pGHR nuclear localization using different pGHR ligands, and we demonstrated that pGHR's nuclear translocation is GH(s)-dependent. We also observed that pGHR translocates into cell nuclei in a pGH dimerization-dependent fashion, whereas further experiments indicated that IMPα/β is involved in the nuclear translocation of the pGH-pGHR dimer. The pGH-pGHR dimer may form a pGH-GHR-JAK2 multiple complex in cell nuclei, which would suggest that similar to its function in the cell membrane, the nuclear-localized pGH-pGHR dimer might still have the ability to signal. •pGH could induce pGHR nuclear translocation in porcine hepatocytes.•GHR translocates into cell nuclei in a GH-dependent fashion.•The nuclear-localized pGH-pGHR dimer might still have the ability to signal.
ISSN:0739-7240
1879-0054
DOI:10.1016/j.domaniend.2017.05.003