Mahmood A, Yamagishi F, Eliakim R, DeSchryver-Kecskemeti K, Gramlich T L, Alpers D H
Gastroenterology Division, Washington University School of Medicine, St. Louis, Missouri 63110.
J Clin Invest. 1994 Jan;93(1):70-80. doi: 10.1172/JCI116986.
To further examine whether surfactant-like particles (DeSchryver-Kecskemeti, K., R. Eliakim, S. Carroll, W. F. Stenson, M. A. Moxley, and D. H. Alpers. 1989. J. Clin. Invest. 84:1355-1361) were involved in the transepithelial transport of lipid, alkaline phosphatase activity and surfactant-like particle content were measured in apical mucosal scrapings, enterocytes, lamina propria, and serum after inhibition of chylomicron transport. Serum triacylglycerol levels were decreased 60-76% by Pluronic L-81, fenfluramine, and choline deficiency compared with fat-fed controls. 5 h after triacylglycerol feed, alkaline phosphatase activity in all three experimental groups was decreased compared with controls by 52-69% in mucosal scrapings and by 33-72% in serum. A parallel decline (60%) in alkaline phosphatase activity occurred in the lamina propria of Pluronic-treated animals. Total particle content (measured by an ELISA using antiserum against purified particle) after Pluronic treatment was decreased in mucosal scrapings, lamina propria, and serum by 16, 22, and 29% at 3 h and by 33, 40, and 8%, respectively, at 5 h after fat feeding. In contrast, particle content was increased in enterocytes by 29% 3 h and by 8% 5 h after fat feeding. By electron microscopy, enterocytes from Pluronic- and fenfluramine-treated animals exhibited a two- to threefold increase in large intracellular cytoplasmic lipid globules and the appearance of lamellae in apposition, with a marked decrease in the number of surfactant-like particles overlying the brush border. These changes, produced by inhibition of chylomicron transport, in the distribution of surfactant-like particles and particle-bound alkaline phosphatase are consistent with a role for these particles in transepithelial triacylglycerol transport across and out of the enterocyte.
为了进一步研究表面活性剂样颗粒(DeSchryver-Kecskemeti, K., R. Eliakim, S. Carroll, W. F. Stenson, M. A. Moxley, and D. H. Alpers. 1989. J. Clin. Invest. 84:1355 - 1361)是否参与脂质的跨上皮转运,在抑制乳糜微粒转运后,测量了顶端黏膜刮片、肠上皮细胞、固有层和血清中的碱性磷酸酶活性及表面活性剂样颗粒含量。与喂食脂肪的对照组相比,普流罗尼克L - 81、芬氟拉明和胆碱缺乏使血清三酰甘油水平降低了60% - 76%。喂食三酰甘油5小时后,所有三个实验组的黏膜刮片中碱性磷酸酶活性与对照组相比降低了52% - 69%,血清中降低了33% - 72%。在普流罗尼克处理的动物固有层中,碱性磷酸酶活性也出现了平行下降(60%)。普流罗尼克处理后,黏膜刮片、固有层和血清中的总颗粒含量(通过使用抗纯化颗粒抗血清的酶联免疫吸附测定法测量)在喂食脂肪后3小时分别降低了16%、22%和29%,5小时分别降低了33%、40%和8%。相比之下,喂食脂肪后3小时肠上皮细胞中的颗粒含量增加了29%,5小时增加了8%。通过电子显微镜观察,普流罗尼克和芬氟拉明处理动物的肠上皮细胞中,大的细胞内细胞质脂质球增加了两到三倍,出现了并列的板层结构,刷状缘上覆盖的表面活性剂样颗粒数量明显减少。由乳糜微粒转运抑制所产生的这些表面活性剂样颗粒和颗粒结合碱性磷酸酶分布的变化,与这些颗粒在三酰甘油跨肠上皮细胞转运并排出肠上皮细胞过程中的作用是一致的。