2002
DOI: 10.1006/jfbi.2001.1858
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Phagocytosis and giant cell formation at 0°C by macrophage (MØ) of Notothenia coriiceps

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Cited by 11 publications
(12 citation statements)
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“…The liquid containing phagocytic cells (macrophages) was aspirated using a Pasteur pipette and centrifuged at 251.5 g for 5 min; the supernatant was discarded. Aliquots of the sediments were examined between a slide and coverslip, under phase contrast microscopy (400×) to determine the phagocytic capacity (PC = number of phagocytosing macrophages/100 macrophages) of the macrophages as described by Silva et al. (2002, 2005)…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The liquid containing phagocytic cells (macrophages) was aspirated using a Pasteur pipette and centrifuged at 251.5 g for 5 min; the supernatant was discarded. Aliquots of the sediments were examined between a slide and coverslip, under phase contrast microscopy (400×) to determine the phagocytic capacity (PC = number of phagocytosing macrophages/100 macrophages) of the macrophages as described by Silva et al. (2002, 2005)…”
Section: Methodsmentioning
confidence: 99%
“…The liquid containing phagocytic cells (macrophages) was aspirated using a Pasteur pipette and centrifuged at 251.5 g for 5 min; the supernatant was discarded. Aliquots of the sediments were examined between a slide and coverslip, under phase contrast microscopy (400·) to determine the phagocytic capacity (PC = number of phagocytosing macrophages ⁄ 100 macrophages) of the macrophages as described by Silva et al (2002Silva et al ( , 2005 Liver and muscle samples (taken from the dorsal superior aspect, 2.0 cm from the left operculum) were collected from the fish. These samples were kept at )10°C and sent for analysis of ether-extracts (according to AOAC -Association of Official Analytical Chemists, 1984) at the Animal Nutrition Analytical Laboratory (Laborato´rio de Ana´lises em Nutric¸a˜o Animal -LANA) of UNESP ⁄ FCAVJ, Jaboticabal, SP.…”
Section: Methodsmentioning
confidence: 99%
“…After centrifugation, the supernatant was discarded and the pellet was resuspended in the remaining liquid and placed on a slide with a coverslip; phagocytes were counted under a phase‐contrast microscope. The number of active phagocytes and the total number of yeast cells inside phagocytic cells were determined, and the phagocytic capacity (PC) and phagocytic index (PI) were calculated according to the method described by Silva, Staines, Hernandez–Blazquez, Porto–Neto and Borges (2002), Silva, Porto–Neto, Borges and Jensch–Junior (2005).…”
Section: Methodsmentioning
confidence: 99%
“…Experiments were carried out in fibreglass tanks (1,000 l) filled with running sea water (1±1.0°C) in a temperature-controlled room at 0±1.0°C at the Biology Laboratories of the Brazilian Antarctic Station, "Comandante Ferraz", in which the recording of biometric data and identification of the fish took place (Silva et al 1998a(Silva et al , 1999. Following anaesthesia with benzocaine (50 ppm; Silva et al 2002), two square (2.0×2.0 cm) fullthickness excision wounds, removing scales, epidermis, dermis, hypoderm and most of the perimysium, were inflicted on both sides of the dorsal-lateral anterior region in each of the 21 fishes. Three fish were used as normal skin controls.…”
Section: Fish Maintenance and Wound Inductionmentioning
confidence: 99%