http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15007
Dopamine in the ink defence system of Sepia officinalis: biosynthesis, vesicular compartmentation in mature ink gland cells, nitric oxide (NO)/cGMP-induced depletion and fate in secreted ink (Articolo in rivista)
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- Label
- Dopamine in the ink defence system of Sepia officinalis: biosynthesis, vesicular compartmentation in mature ink gland cells, nitric oxide (NO)/cGMP-induced depletion and fate in secreted ink (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1042/BJ20031864 (literal)
- Alternative label
Fiore G.; Poli A.; Di Cosmo A.; d'Ischia M.; Palumbo A. (2004)
Dopamine in the ink defence system of Sepia officinalis: biosynthesis, vesicular compartmentation in mature ink gland cells, nitric oxide (NO)/cGMP-induced depletion and fate in secreted ink
in Biochemical journal (Lond., 1984)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Fiore G.; Poli A.; Di Cosmo A.; d'Ischia M.; Palumbo A. (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Zoological Station 'Anton Dohrn', Villa Comunale I-80121, Naples, Italy
Department of Biological and Environmental Sciences, University of Sannio, Via Port'Arsa 11,
I-82100 Benevento, Italy
Department of Organic Chemistry and Biochemistry, University of Naples 'Federico II', Via Cinthia 4, I-80126 Naples, Italy (literal)
- Titolo
- Dopamine in the ink defence system of Sepia officinalis: biosynthesis, vesicular compartmentation in mature ink gland cells, nitric oxide (NO)/cGMP-induced depletion and fate in secreted ink (literal)
- Abstract
- The biosynthesis, localization and fate of catecholamines in the
ink gland of the cuttlefish Sepia officinalis were investigated
by combined biochemical and immunohistocytochemical methodologies.
HPLC analysis of crude ink gland extracts indicated
the presence of dopa (2.18+-0.82 nmol/mg of protein) and DAdiethylamine NONOate (diethylamine diazeniumdiolate), a nitric oxide donor, 8-bromo-cGMP or a guanylyl cyclase inhibitor.
Immunohistochemical results coupled with electron microscopy
indicated that DA was concentrated in vesicles specifically
localized in the mature melanin-producing cells of the ink gland
proximal to the lumen and separated from the melanin-containing
melanosomes. NMDA receptor stimulation or exposure to an NO
donor caused a marked loss of DA immunoreactivity in mature
cells, consistent with a release process. In the lumen of the ink
gland, where mature exhausted cells pour their contents, DA
immunoreactivity was found to be associated with the melanin
granules, due apparently to physical adsorption. Overall, these
results point to DA as a marker of cell maturation in Sepia ink
gland subject to release by the NO/cGMP signalling pathway,
and disclose apparently overlooked DA-melanin interactions in
secreted ink of possible relevance to the defence mechanism.
(dopamine, 0.06+-0.02 nmol/mg of protein), but no detectable
noradrenaline or adrenaline. DA was shown to derive from
L-tyrosine, according to experiments performed by incubating
intact ink glands with [L-14C]tyrosine. The biosynthetic process
involves a tyrosine hydroxylase and a dopa decarboxylase pathway
and is independent of tyrosinase. The tyrosine hydroxylase
activitywas detected under conditions of tyrosinase suppression in
the cytosolic fraction, but not in the melanosomal fraction, of ink
gland extracts, and the presence of the enzyme was confirmed by
Western-blot analysis. Dopa and DA were found to be released
from the ink glands by processes controlled through the NMDAnitric
oxide-cGMP (where NMDA stands for N-methyl-D-aspartate)
signalling pathway, as apparent from incubation experiments
performed with [L-14C]tyrosine in the presence of NMDA,diethylamine NONOate (diethylamine diazeniumdiolate), a nitric
oxide donor, 8-bromo-cGMP or a guanylyl cyclase inhibitor.
Immunohistochemical results coupled with electron microscopy
indicated that DA was concentrated in vesicles specifically
localized in the mature melanin-producing cells of the ink gland
proximal to the lumen and separated from the melanin-containing
melanosomes. NMDA receptor stimulation or exposure to an NO
donor caused a marked loss of DA immunoreactivity in mature
cells, consistent with a release process. In the lumen of the ink
gland, where mature exhausted cells pour their contents, DA
immunoreactivity was found to be associated with the melanin
granules, due apparently to physical adsorption. Overall, these
results point to DA as a marker of cell maturation in Sepia ink
gland subject to release by the NO/cGMP signalling pathway,
and disclose apparently overlooked DA-melanin interactions in
secreted ink of possible relevance to the defence mechanism. (literal)
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