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Nuclear translocation and retention of growth hormone.

Mertani, Hichem C (författare)
Raccurt, Mireille (författare)
Abbate, Aude (författare)
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Kindblom, Jenny, 1971 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
Törnell, Jan (författare)
Billestrup, Nils (författare)
Usson, Yves (författare)
Morel, Gérard (författare)
Lobie, Peter E (författare)
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 (creator_code:org_t)
The Endocrine Society, 2003
2003
Engelska.
Ingår i: Endocrinology. - : The Endocrine Society. - 0013-7227 .- 1945-7170. ; 144:7, s. 3182-95
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We have previously demonstrated that GH is subject to rapid receptor-dependent nuclear translocation. Here, we examine the importance of ligand activation of the GH-receptor (GHR)-associated Janus kinase (JAK) 2 and receptor dimerization for hormone internalization and nuclear translocation by use of cells stably transfected with cDNA for the GHR. Staurosporine and herbimycin A treatment of cells did not affect the ability of GH to internalize but resulted in increased nuclear accumulation of hormone. Similarly, receptor mutations, which prevent the association and activation of JAK2, did not affect the ability of the hormone to internalize or translocate to the nucleus but resulted in increased nuclear accumulation of GH. These results were observed both by nuclear isolation and confocal laser scanning microscopy. Staurosporine treatment of cells in which human GH (hGH) was targeted to the cytoplasm (removal of secretion sequence) or to the nucleus (addition of the nuclear localization sequence of SV40 large T antigen) resulted in preferential accumulation of hGH in the nucleus. We further investigated the requirement of receptor dimerization for GH nuclear translocation using the non-receptor-dimerizing hGH antagonist, hGH-G120R, conjugated to fluorescein isothiocyanate. Confocal laser scanning microscopy demonstrated efficient internalization of both hGH and hGH-G120R but lack of nuclear translocation of hGH-G120R. Thus, we conclude that activation of JAK2 kinase and the subsequent tyrosine phosphorylation is not required for nuclear translocation of GH but is pivotal for the removal of the hormone from the nucleus, and that GH translocates into the nucleus in a GHR dimerized-dependent fashion.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

Active Transport
Cell Nucleus
physiology
Amino Acid Sequence
Animals
CHO Cells
Cell Nucleus
metabolism
Cricetinae
Cytoplasm
metabolism
DNA
Complementary
Dimerization
Enzyme Inhibitors
pharmacology
Enzyme-Linked Immunosorbent Assay
Gene Deletion
Growth Hormone
metabolism
Janus Kinase 2
Ligands
Microscopy
Confocal
Molecular Sequence Data
Mutagenesis
Protein-Tyrosine Kinases
antagonists & inhibitors
metabolism
Proto-Oncogene Proteins
Rats
Receptors
Cell Surface
chemistry
genetics
metabolism
Receptors
Somatotropin
chemistry
genetics
metabolism
Staurosporine
pharmacology
Transfection

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