Phillips A D, Brown A, Hicks S, Schüller S, Murch S H, Walker-Smith J A, Swallow D M
Centre for Paediatric Gastroenterology, Department of Paediatrics and Child Health, Royal Free Hospital, Pond St, London NW3 2QG, UK.
Gut. 2004 Dec;53(12):1764-71. doi: 10.1136/gut.2004.041954.
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.
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.
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.
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.
微绒毛萎缩是婴儿期难治性腹泻的一种疾病,其特征为肠上皮细胞异常,表现为顶端细胞质内周期性酸-希夫(PAS)阳性分泌颗粒异常积聚以及微绒毛包涵体的存在。PAS阳性物质的性质尚不清楚,本文旨在进一步研究其组成。
用甲醛固定切片,用阿尔辛蓝/PAS染色以确定该物质的酸性或中性性质,采用苯肼阻断法特异性染色唾液酸,皂化反应确定唾液酸乙酰化的存在。用稀硫酸消化测试唾液酸染色的特异性。通过免疫化学方法检测血型相关抗原的表达。
阿尔辛蓝/PAS染色显示对照组中原本中性(PAS阳性)的刷状缘上有一层紧密相邻的酸性物质。在微绒毛萎缩中,可见三层结构,外层为酸性层,中间为未染色的刷状缘区域,上皮内积聚一种含有乙酰化唾液酸的中性糖物质。对照组中在刷状缘、黏液和杯状细胞内检测到血型抗原。在微绒毛萎缩中,它们还在上皮细胞的顶端细胞质内表达,与PAS异常情况相似。免疫电子显微镜将表达定位到分泌颗粒。
微绒毛萎缩时,一种含有乙酰化唾液酸的中性、血型抗原阳性的糖物质在上皮内积聚。先前的研究表明,在这种疾病中直接和间接组成途径是完整的,推测异常染色模式反映了糖萼相关物质的积聚。