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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。

Characterization of isolated villus and crypt cells from the small intestine of the adult mouse.

作者信息

Pothier P, Hugon J S

出版信息

Cell Tissue Res. 1980;211(3):405-18. doi: 10.1007/BF00234396.

Abstract

Suspensions of sequentially isolated villus and crypt cells were obtained in order to study certain biochemical changes associated with differentiation of epithelial cells in the small intestine of the mouse. Microscopic observation of the various cell fractions reveals that the epithelial cells detach as individual cells or small sheets of epithelium from the tip to the base of the villus, whereas cells in the crypt regions are separated as entire crypt units. The isolated cells retain their ultrastructural integrity as judged by electron miscroscopy. Chemical characterization of the various fractions shows that the total cellular protein content, expressed in activity per cell, remains relatively constant throughout the villus region followed by a noticeable drop in the crypt zone. On the other hand, sharp variations in values of cell DNA content are observed in the crypt zone depending on the reference of activity being used. Activity profiles of several brush border enzymes confirm the biochemical changes that occur during the migration of cells from the crypt to the villus tip, as observed in other species, with maximum activity of sucrase in the mid-villus region, of glucoamylase, trehalase, lactase and maltase in the upper third region, and of alkaline phosphatase at the villus tip. Forty-eight-hour suspension cultures of cell fractions corresponding to cells at the base of the villus and crypt zones show a moderate decrease in protein and enzyme activities to approximately 70% of their original value, with DNA content remaining stable throughout the incubation period. The use of biochemical activities as indicators of cellular integrity during cell culture is discussed.

摘要

为了研究与小鼠小肠上皮细胞分化相关的某些生化变化,制备了依次分离的绒毛细胞和隐窝细胞悬液。对各种细胞组分的显微镜观察显示,上皮细胞从绒毛顶端到基部以单个细胞或小上皮片的形式脱离,而隐窝区域的细胞则作为完整的隐窝单元分离。通过电子显微镜判断,分离的细胞保持其超微结构完整性。对各种组分的化学表征表明,以每细胞活性表示的总细胞蛋白含量在整个绒毛区域保持相对恒定,随后在隐窝区域明显下降。另一方面,根据所使用的活性参考,在隐窝区域观察到细胞DNA含量值的急剧变化。几种刷状缘酶的活性谱证实了细胞从隐窝迁移到绒毛顶端过程中发生的生化变化,正如在其他物种中观察到的那样,蔗糖酶在绒毛中部区域活性最高,葡糖淀粉酶、海藻糖酶、乳糖酶和麦芽糖酶在上三分之一区域活性最高,碱性磷酸酶在绒毛顶端活性最高。对绒毛基部和隐窝区域细胞对应的细胞组分进行48小时的悬浮培养,结果显示蛋白质和酶活性适度下降至其原始值的约70%,而DNA含量在整个培养期间保持稳定。本文讨论了在细胞培养过程中使用生化活性作为细胞完整性指标的问题。

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