| Acetylated sialic acid residues and blood group antigens localise within the epithelium in microvillous atrophy indicating internal accumulation of the glycocalyx. | |
| | |
MedLine Citation:
|
PMID: 15542511 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
BACKGROUND: Microvillous atrophy, a disorder of intractable diarrhoea in infancy, is characterised by the intestinal epithelial cell abnormalities of abnormal accumulation of periodic acid-Schiff (PAS) positive secretory granules within the apical cytoplasm and the presence of microvillous inclusions. The identity of the PAS positive material is not known, and the aim of this paper was to further investigate its composition. METHODS: Formaldehyde fixed sections were stained with alcian blue/PAS to identify the acidic or neutral nature of the material, phenylhydrazine blocking was employed to stain specifically for sialic acid, and saponification determined the presence of sialic acid acetylation. The specificity of sialic acid staining was tested by digestion with mild sulphuric acid. Expression of blood group related antigens was tested immunochemically. RESULTS: Alcian blue/PAS staining identified a closely apposed layer of acidic material on the otherwise neutral (PAS positive) brush border in controls. In microvillous atrophy, a triple layer was seen with an outer acidic layer, an unstained brush border region, and accumulation within the epithelium of a neutral glycosubstance that contained acetylated sialic acid. Blood group antigens were detected on the brush border, in mucus, and within goblet cells in controls. In microvillous atrophy they were additionally expressed within the apical cytoplasm of epithelial cells mirroring the PAS abnormality. Immuno electron microscopy localised expression to secretory granules. CONCLUSIONS: A neutral, blood group antigen positive, glycosubstance that contains acetylated sialic acid accumulates in the epithelium in microvillous atrophy. Previous studies have demonstrated that the direct and indirect constitutive pathways are intact in this disorder and it is speculated that the abnormal staining pattern reflects accumulation of glycocalyx related material. |
| | |
Authors:
|
A D Phillips; A Brown; S Hicks; S Schüller; S H Murch; J A Walker-Smith; D M Swallow |
Publication Detail:
|
Type: Journal Article |
Journal Detail:
|
Title: Gut Volume: 53 ISSN: 0017-5749 ISO Abbreviation: Gut Publication Date: 2004 Dec |
Date Detail:
|
Created Date: 2004-11-15 Completed Date: 2004-12-14 Revised Date: 2009-11-18 |
Medline Journal Info:
|
Nlm Unique ID: 2985108R Medline TA: Gut Country: England |
Other Details:
|
Languages: eng Pagination: 1764-71 Citation Subset: AIM; IM |
Affiliation:
|
Centre for Paediatric Gastroenterology, Department of Paediatrics and Child Health, Royal Free Hospital, Pond St, London NW3 2QG, UK. adphill@rfc.ucl.ac.uk |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
ABO Blood-Group System
/
metabolism Atrophy / congenital, metabolism Blood Group Antigens / metabolism* Child, Preschool Diarrhea / metabolism, pathology Female Glycocalyx / metabolism* Humans Infant Intestinal Mucosa / metabolism, pathology* Intestine, Small / metabolism, pathology Lewis Blood-Group System / metabolism Male Microscopy, Electron Microvilli / pathology Sialic Acids / metabolism* |
| Chemical | |
Reg. No./Substance:
|
0/ABO Blood-Group System; 0/Blood Group Antigens; 0/Lewis Blood-Group System; 0/Sialic Acids |
| Comments/Corrections | |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Helicobacter pylori test and eradicate versus prompt endoscopy for management of dyspeptic patients:...
Next Document: Depletion of intestinal resident macrophages prevents ischaemia reperfusion injury in gut.