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人十二指肠黏膜中肠激酶的亚细胞定位

Subcellular localization of enterokinase in human duodenal mucosa.

作者信息

Lobley R W, Franks R, Holmes R

出版信息

Clin Sci Mol Med. 1977 Dec;53(6):551-62. doi: 10.1042/cs0530551.

Abstract
  1. Specimens of human duodenal mucosa were obtained at duodenotomy. Superficial mucosal scrapings were homogenized in isotonic sucrose solution and fractionated by differential centrifugation. The distribution of organelles among the subcellular fractions was monitored by assay of suitable marker enzymes. 2. Enterokinase was recovered predominantly in the nuclear+brush-border fraction and 80% of the total activity was found to be particulate; approximately 20% of the enzyme was present in the soluble fraction, compared with 1% of the brush-border markers sucrase and alkaline phosphatase. 3. The brush-border-containing fraction was subfractionated by treatment with hypertonic Tris followed by differential and density gradient centrifugation. Enterokinase was distributed among the subfractions in parallel with brush-border markers and was concentrated in a subfraction which was highly enriched in microvillous membranes. 4. It was concluded that enterokinase is localized primarily to the microvillous membrane of the epithelial cell brush border in man, but that in addition a proportion of the enzyme may be present in a soluble or easily released form in the duodenal mucosa.
摘要
  1. 在十二指肠切开术中获取人十二指肠黏膜标本。将表层黏膜刮片在等渗蔗糖溶液中匀浆,然后通过差速离心进行分级分离。通过测定合适的标志酶来监测细胞器在亚细胞组分中的分布。2. 肠激酶主要在细胞核 + 刷状缘组分中回收,发现总活性的80%为颗粒状;与刷状缘标志物蔗糖酶和碱性磷酸酶的1%相比,约20%的酶存在于可溶性组分中。3. 通过用高渗Tris处理,然后进行差速和密度梯度离心,对含刷状缘的组分进行进一步分级分离。肠激酶与刷状缘标志物平行分布在各亚组分中,并集中在一个高度富含微绒毛膜的亚组分中。4. 得出的结论是,在人类中,肠激酶主要定位于上皮细胞刷状缘的微绒毛膜,但此外,一部分酶可能以可溶性或易于释放的形式存在于十二指肠黏膜中。

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