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小鼠小肠隐窝细胞的分离

Crypt cell isolation in the small intestine of the mouse.

作者信息

Kremski V C, Varani L, DeSaive C, Miller P, Nicolini C

出版信息

J Histochem Cytochem. 1977 Jul;25(7):554-9. doi: 10.1177/25.7.894003.

DOI:10.1177/25.7.894003
PMID:894003
Abstract

A successful method has been developed for isolating viable single cell suspensions of intestinal crypt cells from the small bowel of the mouse. The lumen of the intestine was perfused with a 0.2% trypsin solution that dissociated the lining epithelial cells. Crypt cell isolation, which proves to be extremely critical, occurred under optimal mechanical and chemical configurations about 75 min after the beginning of the procedure.

摘要

已开发出一种成功的方法,用于从小鼠小肠中分离出具有活性的肠隐窝细胞单细胞悬液。用0.2%的胰蛋白酶溶液灌注肠腔,以使内衬上皮细胞解离。隐窝细胞的分离在该程序开始约75分钟后,在最佳的机械和化学条件下进行,这一过程被证明极为关键。

相似文献

1
Crypt cell isolation in the small intestine of the mouse.小鼠小肠隐窝细胞的分离
J Histochem Cytochem. 1977 Jul;25(7):554-9. doi: 10.1177/25.7.894003.
2
A novel alkaline phosphatase-based isolation method allows characterization of intraepithelial lymphocytes from villi tip and crypt regions of murine small intestine.一种基于碱性磷酸酶的新型分离方法能够对来自小鼠小肠绒毛顶端和隐窝区域的上皮内淋巴细胞进行表征。
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Characterization of isolated epithelial cells from rat small intestine.
Am J Physiol. 1982 Feb;242(2):G147-55. doi: 10.1152/ajpgi.1982.242.2.G147.
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Comparative viabilities of rat intestinal epithelial cells prepared by mechanical, enzymatic and chelating methods.通过机械、酶解和螯合方法制备的大鼠肠上皮细胞的比较活力。
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Improved isolation methods for mucosal leukocytes from small and large intestines in rats.大鼠小肠和大肠黏膜白细胞的改良分离方法。
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Isolation of intestinal villus and crypt cells suitable for 'in vitro' studies [proceedings].适合“体外”研究的肠绒毛和隐窝细胞的分离[会议论文集]
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Characterization of isolated villus and crypt cells from the small intestine of the adult mouse.
成年小鼠小肠中分离出的绒毛细胞和隐窝细胞的特性分析。
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Stability of enterocytes and certain enzymatic activities in suspensions of cells from the villous tip to the crypt of Lieberkühn of the mouse small intestine.小鼠小肠从绒毛顶端到利伯kühn隐窝的细胞悬液中肠上皮细胞的稳定性和某些酶活性
Appl Environ Microbiol. 1988 Oct;54(10):2398-404. doi: 10.1128/aem.54.10.2398-2404.1988.