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普通可变免疫缺陷肠病的空肠黏膜酶活性、调节肽及细胞器病理学

Jejunal mucosal enzyme activities, regulatory peptides and organelle pathology of the enteropathy of common variable immunodeficiency.

作者信息

Dawson J, Bryant M G, Bloom S R, Peters T J

出版信息

Gut. 1986 Mar;27(3):273-7. doi: 10.1136/gut.27.3.273.

Abstract

Jejunal biopsies from six patients having the small bowel enteropathy associated with common variable immunodeficiency have been subjected to analytical subcellular fractionation and enzymic and regulatory peptide microassay to define the organelle pathology of this syndrome. Compared with normal subjects, the immunodeficient patients had decreased activities of the three brush border enzymes: alkaline phosphatase, gamma-glutamyl transferase and alpha-glucosidase. The other organelle marker enzyme activities and all the regulatory peptide concentrations did not differ from the controls. Density gradient experiments showed a complete loss of particulate beta-glucosidase (lactase) with activity entirely located in the cytosol. The integrity of other organelles was normal. These data indicate that the enteropathy of common variable immunodeficiency is associated with abnormalities in the jejunal brush border analogous to those present in tropical malabsorption syndrome.

摘要

对6例患有与常见可变免疫缺陷相关的小肠肠病患者的空肠活检组织进行了亚细胞分级分离分析以及酶和调节肽微量测定,以确定该综合征的细胞器病理学特征。与正常受试者相比,免疫缺陷患者的三种刷状缘酶(碱性磷酸酶、γ-谷氨酰转移酶和α-葡萄糖苷酶)活性降低。其他细胞器标记酶活性和所有调节肽浓度与对照组无差异。密度梯度实验显示颗粒状β-葡萄糖苷酶(乳糖酶)完全缺失,其活性完全位于胞质溶胶中。其他细胞器的完整性正常。这些数据表明,常见可变免疫缺陷的肠病与空肠刷状缘异常有关,类似于热带吸收不良综合征中出现的异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e731/1433437/fee5c3d0e42d/gut00363-0050-a.jpg

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