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首页> 外文期刊>Biological & pharmaceutical bulletin >Asiatic Acid, Corosolic Acid, and Maslinic Acid Interfere with Intracellular Trafficking and N-Linked Glycosylation of Intercellular Adhesion Molecule-1
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Asiatic Acid, Corosolic Acid, and Maslinic Acid Interfere with Intracellular Trafficking and N-Linked Glycosylation of Intercellular Adhesion Molecule-1

机译:亚洲酸,凝纹酸和唾液酸干扰细胞内运输和细胞间粘附分子-1的n键合糖基化

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摘要

The pentacyclic triterpenoid ursolic acid was previously shown to inhibit the intracellular trafficking of intercellular adhesion molecule-1 (ICAM-1) from the endoplasmic reticulum (ER) to the Golgi apparatus. In the present study, we further investigated the biological activities of three pentacyclic triterpenoids closely related to ursolic acid on the interleukin 1 alpha-induced expression and intracellular trafficking of ICAM-1. In human lung adenocarcinoma A549 cells, asiatic acid, corosolic acid, and maslinic acid interfered with the intracellular transport of ICAM-1 to the cell surface. Endoglycosidase H-sensitive glycans were linked to ICAM-1 in asiatic acid-, corosolic acid-, and maslinic acid-treated cells. Unlike corosolic acid, asiatic acid and maslinic acid increased the amount of the ICAM-1 protein. Moreover, asiatic acid increased the co-localization of ICAM-1 with calnexin (an ER marker), but not GM130 (a cis-Golgi marker). Asiatic acid, corosolic acid, and maslinic acid inhibited yeast alpha-glucosidase activity, but not Jack bean alpha-mannosidase activity. These results indicate that asiatic acid, corosolic acid, and maslinic acid interfere with the intracellular transport of ICAM-1 to the cell surface and cause the accumulation of ICAM-1 linked to endoglycosidase H-sensitive glycans.
机译:先前所示,戊氰酸丙二萜胶酸尿酸尿酸抑制来自内质网(ER)的细胞间粘附分子-1(ICAM-1)到GOLGI装置。在本研究中,我们进一步研究了三个五胞苷三萜类化合物与白细胞介素1α-诱导的表达和细胞内运输密切相关的三种五胞苷三萜类化合物的生物学活性。在人肺腺癌A549细胞中,亚氨酸,凝胶酸和唾液酸干扰了ICAM-1的细胞内传输到细胞表面。内皮糖苷酶H敏感聚糖与Asianic酸 - ,凝胶酸 - 和唾液酸处理的细胞中的ICAM-1连接。与凝胶酸,亚洲酸和唾液酸不同,增加了ICAM-1蛋白的量。此外,亚洲酸增加了Calnexin(ER标记)的ICAM-1的共定位,但不是GM130(CIS-GOLGI标记)。亚洲酸,凝胶酸和唾液酸抑制酵母α-葡糖苷酶活性,但不是千烷豆α-甘露糖苷酶活性。这些结果表明,亚氨酸,凝纹酸和唾液酸干扰了ICAM-1的细胞内传输到细胞表面,并导致ICAM-1与内甘油糖苷酶H敏化聚糖的积累进行了累积。

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