2006
DOI: 10.1016/j.aquaculture.2006.09.021
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Characterisation of cell types in abalone (Haliotis spp.) tissues using immunohistochemical techniques

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Cited by 7 publications
(6 citation statements)
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“…Cyclin D1 is widely used as a histopathological marker in many tissues as it an important regulator of the cell cycle progression from G1 to S phase. In normal tissues, its expression is well regulated, while the highly expressed cyclin D1 might be a good surrogate to genotoxicity as it refers to the deregulation of the cell cycle [ 49 , 50 ]. In this research, adult snails that were exposed to sublethal concentrations of C. procera or A. halimus had anomalies in their digestive and hermaphrodite glands.…”
Section: Discussionmentioning
confidence: 99%
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“…Cyclin D1 is widely used as a histopathological marker in many tissues as it an important regulator of the cell cycle progression from G1 to S phase. In normal tissues, its expression is well regulated, while the highly expressed cyclin D1 might be a good surrogate to genotoxicity as it refers to the deregulation of the cell cycle [ 49 , 50 ]. In this research, adult snails that were exposed to sublethal concentrations of C. procera or A. halimus had anomalies in their digestive and hermaphrodite glands.…”
Section: Discussionmentioning
confidence: 99%
“…The molluscicidal activity of C. procera and A. halimus may be related to the presence of high levels of fatty acids, particularly palmitic acid, which has been reported to be responsible for the killing of Pomacea canaliculata snails [ 51 ]. The immunohistochemical analysis relies on specific interactions between antibodies and their target antigens [ 49 , 50 ]. Cyclin D1 controls how far along the cell cycle it is allowed to go.…”
Section: Discussionmentioning
confidence: 99%
“…vesicular round to oval large nuclei with evident nucleoli), but showed nuclear PCNA immunostaining in early phases of the disease, while in advanced stages they showed predominantly cytoplasmic labelling. It is known that PCNA is also ex pressed during the cell cycle in proliferating cells of molluscs (Marigómez et al 1999, Hanselmann et al 2000, Harris et al 2006, Franco et al 2010: PCNA levels increase during the G1-S phase of the cell cycle, and usually localize in the nucleus, being involved in cell proliferation control and DNA repair (Paunesku et al 2001). However, recent studies in human granulocytes suggest that PCNA could be also involved in suppressing apoptosis when localized in the cytoplasm, where it binds to and inhibits the procaspases, which are key molecules in apoptosis control (Witko-Sarsat et al 2010); interestingly, this pattern has also been ob - Lanza (1980) and Bartl et al (1984) served in human Hodgkin's lymphoma (Benjamin & Gown 1991).…”
Section: Discussionmentioning
confidence: 99%
“…PCNA immunohistochemistry and quantification were made according to previous reports (Maiolino et al 1995, De Vico et al 1996 with slight modifica- tion, using a mouse monoclonal antibody against PCNA, clone PC10 (Sigma), which was already successfully tested to localize proliferating cells in several mollusc species, including Mytilus galloprovincialis (Mari gómez et al 1999, Hanselmann et al 2000, Harris et al 2006, Franco et al 2010. Briefly, after deparaffinization of the tissue sections, endogenous peroxidase was blocked by incubation in H 2 O 2methanol (4:1) for 20 min.…”
Section: Methodsmentioning
confidence: 99%
“…Interestingly, intersex also shows a positive correlation with PCNA and Avon sampling site (Figure 3). Increased PCNA protein expression has previously been detected in histologically normal (Marigomez et al, 1999;Hanselmann et al, 2000;Harris et al, 2006;Franco et al, 2010) and neoplastic (Carella et al, 2013) mollusc tissues. In contrast, PCNA down regulation has been reported in gill tissue of mussels experimentally exposed to metals (Varotto et al, 2013).…”
Section: Discussionmentioning
confidence: 85%