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在可渗透支持物上进行静态原代单层培养的未成熟大鼠附睾上皮细胞。I. 向量分泌

Immature rat epididymal epithelial cells grown in static primary monolayer culture on permeable supports. I. Vectorial secretion.

作者信息

Cooper T G, Yeung C H, Meyer R

机构信息

Max Planck Clinical Research Unit for Reproductive Medicine, University of Münster, Federal Republic of Germany.

出版信息

Cell Tissue Res. 1989 Jun;256(3):567-72. doi: 10.1007/BF00225605.

Abstract

A cell culture system is characterized for monolayers of immature rat epididymal epithelial cells grown on permeable supports. Cover of the filters was achieved by days 4-5 and was maintained for 9-12 days. The secretion of acid phosphatase (ACP), alkaline phosphatase (AKP) and N-acetylglucosaminidase (NAG) into apical and basal compartments of culture chambers was monitored with time in culture for cells from the proximal and distal epididymis of 37-day-old animals. There was independent secretion of the three enzymes: secretion of NAG and AKP was mainly apical, that of ACP basal; daily secretion of ACP and AKP was constant throughout culture, that of NAG declined; there was greater secretion of NAG and AKP by cells from the proximal than the distal region. The initial high apical secretion of NAG is thought to reflect loss of enzyme from unattached cells, whereas the later AKP secretion is truly directional. Secretion was not influenced by the enzymes used in cell preparation. The cytotoxic agent Thimerosal inhibited secretion of all enzymes when placed beneath the cultures, indicating that secretion depended on viable cells, but initially stimulated release of AKP when applied above the cells possibly reflecting release from the cell membrane.

摘要

一种细胞培养系统的特征在于,未成熟大鼠附睾上皮细胞单层生长在可渗透支持物上。在第4 - 5天实现滤器覆盖,并维持9 - 12天。监测来自37日龄动物近端和远端附睾的细胞在培养过程中,酸性磷酸酶(ACP)、碱性磷酸酶(AKP)和N - 乙酰氨基葡萄糖苷酶(NAG)向培养室顶端和基底隔室的分泌随时间的变化。这三种酶的分泌是独立的:NAG和AKP的分泌主要是顶端分泌,ACP是基底分泌;在整个培养过程中,ACP和AKP的每日分泌量恒定,NAG的分泌量下降;近端区域细胞分泌的NAG和AKP比远端区域更多。NAG最初较高的顶端分泌被认为反映了未附着细胞中酶的流失,而后期AKP的分泌是真正的定向分泌。分泌不受细胞制备中使用的酶的影响。细胞毒性剂硫柳汞置于培养物下方时会抑制所有酶的分泌,表明分泌依赖于活细胞,但当应用于细胞上方时最初会刺激AKP的释放,这可能反映了从细胞膜的释放。

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