http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37439
Localisation of the human oxytocin receptor in caveolin-1 enriched domains turns the receptor-mediated inhibition of cell growth into a proliferative response. (Articolo in rivista)
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- Label
- Localisation of the human oxytocin receptor in caveolin-1 enriched domains turns the receptor-mediated inhibition of cell growth into a proliferative response. (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Guzzi F., Zanchetta D., Cassoni P., Guzzi V., Francolini M., Parenti M., Chini B. (2002)
Localisation of the human oxytocin receptor in caveolin-1 enriched domains turns the receptor-mediated inhibition of cell growth into a proliferative response.
in Oncogene (Basingstoke)
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- Guzzi F., Zanchetta D., Cassoni P., Guzzi V., Francolini M., Parenti M., Chini B. (literal)
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- ISI Web of Science (WOS) (literal)
- Titolo
- Localisation of the human oxytocin receptor in caveolin-1 enriched domains turns the receptor-mediated inhibition of cell growth into a proliferative response. (literal)
- Abstract
- In this study, we investigated the functional role of the localisation of
human OTR in caveolin-1 enriched membrane domains. Biochemical
fractionation of MDCK cells stably expressing the WT OTR-GFP indicated
that only minor quantities of receptor are partitioned in caveolin-1
enriched domains. However, when fused to caveolin-2, the OTR protein
proved to be exclusively localised in caveolin-1 enriched fractions, where
it bound the agonist with increased affinity and efficiently coupled to
Gaq/11. Interestingly, the chimeric protein was unable to undergo agonist-
induced internalisation and remained confined to the plasma membrane even
after prolonged agonist exposure (120 min). A striking difference in
receptor stimulation was observed when the OT-induced effect on cell
proliferation was analysed: stimulation of the human WT OTR inhibited cell
growth, whereas the chimeric protein had a proliferative effect. These
data indicate that the localisation of human OTR in caveolin-1 enriched
microdomains radically alters its regulatory effects on cell growth; the
fraction of OTR residing in caveolar structures may therefore play a
crucial role in regulating cell proliferation. (literal)
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