1960
DOI: 10.1177/8.3.200
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Esterase Activity in Leukocytes Demonstrated by the Use of Naphthol as-D Chloroacetate Substrate

Abstract: Gouuiori (4) in 1953 pointed out that the substrate uuaphutiiol AS chboro:ocetate gave entirely olifferemut histochuemuuio'al pictures of estertose activity itu tissuo's thuauu the regulttr naphuthol aoetates, anb with this substrate hue miO)t('(l strikimug staining reaotions in normal and leukemic iueutrophuihie leukocyto's. Recently * This ituVe-sIigtotio)tt us-its uipporteol IIy a research grtomut (AI-30-l) 1571 from the Atomic Euuergy Conunuuis-siolnu tomud NIH granul C.Y. 4724. t Part lv sumtlllolrtcoh hI… Show more

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Cited by 363 publications
(103 citation statements)
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“…Frozen sections from normal and rheumatoid synovial tissue and cytocentrifuge preparations of cells obtained from normal and rheumatoid synovial specimens were investigated for the presence of acid alpha-naphtyl acetate esterase (ANAE) (22), naphthol AS-D acetate esterase (NASDAE), inhibitable by sodium fluoride (NaF) (23,24), and naphthol AS-D chloroacetate esterase (NASDCAE) (25). ATPase staining was performed on normal suspended synoviocytes (26).…”
Section: Sources Of Tissuementioning
confidence: 99%
“…Frozen sections from normal and rheumatoid synovial tissue and cytocentrifuge preparations of cells obtained from normal and rheumatoid synovial specimens were investigated for the presence of acid alpha-naphtyl acetate esterase (ANAE) (22), naphthol AS-D acetate esterase (NASDAE), inhibitable by sodium fluoride (NaF) (23,24), and naphthol AS-D chloroacetate esterase (NASDCAE) (25). ATPase staining was performed on normal suspended synoviocytes (26).…”
Section: Sources Of Tissuementioning
confidence: 99%
“…To visualize mast cells, frozen sections were air-dried for ϳ30 min, post-fixed in ice-cold acetone for 10 min, rinsed in PBS, and then stained in either Toluidine blue (a metachromatic dye for mast cells, made up as 0.1% Toluidine blue O (Sigma) in 1% sodium chloride, pH 2.3), Csaba stain (Alcian blue/Safranin O, an amine/heparin stain for mast cells, made up as 0.36% Alcian blue (Sigma), 0.018% Safranin O (Sigma) in acetate buffer, pH 1.42), or by using an enzymatic reaction with naphthol AS-D chloroacetate esterase (Sigma) to detect chymase activity (16), then counterstained with Gill's hematoxylin or DAPI. For inhibitor-localization, frozen sections were prepared as above, then incubated overnight with 50 nM ecotinPKal (10) biotinylated with Sulfo-NHS-LC-LC biotin (EZ-Link, Pierce), followed by 1-h incubation with Alexa 488-conjugated streptavidin (Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…Plasma Kallikrein Specifically Localizes to Mast Cell Granules-To determine the subcellular localization of ecotinPKal in mast cells, we co-stained cells for chymase activity using naphthol chloroacetate esterase, a marker of mast cell granule chymase that appears red in both brightfield and fluorescent microscopy (16). PKal localized to the cytoplasmic granules of mast cells in wild-type mice (Fig.…”
Section: Ecotin-pkal Is Specific For Human and Mouse Plasmamentioning
confidence: 99%
“…Histochemical stain for the chloroacetate esterase (Leder) stain was performed. 30 Immunohistochemical stains were performed for CD3, CD20, myeloperoxidase (DAKO) and CD34 (Navocastra) on the above-mentioned selected slides. The immunoperoxidase technique with microwave antigen retrieval was used.…”
Section: Methodsmentioning
confidence: 99%