Stirling C E, Schneider A J, Wong M D, Kinter W B
J Clin Invest. 1972 Feb;51(2):438-51. doi: 10.1172/JCI106830.
Both galactose accumulation and phlorizin binding by columnar epithelial cells have been investigated in vitro with a recently developed technique for high-resolution, plastic-section radioautography which is particularly suited to small quantities of biopsy tissue. Grain density analysis of the radioautographs provides definitive support for the view that the cellular mechanisms underlying glucose-galactose absorption in laboratory animals are fully applicable to the small intestine of man. Even the number of sugar carriers at the microvillar membrane appears similar and the major quantitative difference, lower affinity for phlorizin in man, correlates with the finding that phlorizin is also a less potent inhibitor of uphill, galactose transport at the microvilli. In addition, radioautographs of biopsies taken 2 yr apart from a patient with glucose-galactose malabsorption provide evidence that the cellular defect in this inborn error of transport is a persistent reduction in the number of functioning sugar carriers at the microvillar membrane.
利用一种最近开发的高分辨率塑料切片放射自显影技术,已在体外对柱状上皮细胞中半乳糖积累和根皮苷结合情况进行了研究,该技术特别适用于少量活检组织。放射自显影片的颗粒密度分析为以下观点提供了确凿支持:实验动物中葡萄糖 - 半乳糖吸收的细胞机制完全适用于人类小肠。甚至微绒毛膜上糖载体的数量看起来也相似,主要的定量差异在于人类对根皮苷的亲和力较低,这与根皮苷也是微绒毛上半乳糖逆向转运的较弱抑制剂这一发现相关。此外,对一名葡萄糖 - 半乳糖吸收不良患者相隔两年所取活检组织的放射自显影片显示,这种先天性转运缺陷中的细胞缺陷是微绒毛膜上功能性糖载体数量持续减少。