1992
DOI: 10.1177/40.3.1552177
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Lectin cytochemistry in the gastrointestinal tract with special reference to glycosylation in the Golgi apparatus of Brunner's gland cells.

Abstract: Two hydrophilic, low temperature-embedding resins, Lowia y 1 K4hf and LR White, were compared in lectin cytochemistry. Post-embedding staining of colloidal gold-labeled G a onia symplicZolia agglutinin II (GSA-11) resulted in staining of the Golgi apparatus and mucous granules of mucous neck cells in the gastric fundic gland, pylorocytes, and Brunner's gland cells embedded in either resin, although it was much easier to make ultra-thin sections with LR White-embedded mate-rial than with the other. Post-furatio… Show more

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Cited by 31 publications
(26 citation statements)
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References 18 publications
(28 reference statements)
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“…This conclusion is based on the fact that three mucous neck cell markers (TFF2/GSII/MUC6, as shown here and previously [26][27][28][29] ), but not Cdx2, labeled this expanded compartment in both animal models. Previously, gastric mucosal changes with histological features of Brunner's gland cells were designated as metaplastic.…”
Section: Discussionsupporting
confidence: 79%
“…This conclusion is based on the fact that three mucous neck cell markers (TFF2/GSII/MUC6, as shown here and previously [26][27][28][29] ), but not Cdx2, labeled this expanded compartment in both animal models. Previously, gastric mucosal changes with histological features of Brunner's gland cells were designated as metaplastic.…”
Section: Discussionsupporting
confidence: 79%
“…Immunoelectron microscopy was performed essentially as described by Suzuki and Kataoka (1992) and Tomoyasu et al (1993b), except that the leaves were cut into 1 Ï« 1-mm pieces and fixed with 0.1% glutaraldehyde and 4% paraformaldehyde in sodium cacodylate, pH 7.4, under vacuum conditions. The tissues were embedded in London Resin White (London Resin Co., London, UK) at ÏȘ20ЊC.…”
Section: Immunoelectron Microscopymentioning
confidence: 99%
“…After 5 rain, the ceils were harvested and resuspended in the same fixative solution buffered with 50 mM sodium eacodylate (pH 7.2) for 1 h. The cells were dehydrated with an ethanol series and embedded in London Resin white (Suzaki et al 1992). Ultrathin sections were mounted on uncoated gold grids and used for immunostaining and in situ hybridization.…”
Section: Sample Preparation For Electron Microscopymentioning
confidence: 99%