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氯喹对培养的未成熟大鼠支持细胞紧密连接形成的影响。

Effect of chloroquine on the formation of tight junctions in cultured immature rat Sertoli cells.

作者信息

Okanlawon A, Dym M

机构信息

Department of Cell Biology, Georgetown University Medical Center, Washington, D.C. 20007, USA.

出版信息

J Androl. 1996 May-Jun;17(3):249-55.

PMID:8792215
Abstract

Adjoining immature Sertoli cells in the seminiferous epithelium form a tight junctional complex leading to the development of the blood-testis barrier. Protease and antiprotease activities have been implicated in the process of formation of tight junctions. Here, we report the effect of chloroquine, an antimalarial drug with antiprotease activity, on the development of intercellular tight junctions in cultured immature rat Sertoli cells. For positive control, the classical lysosomotropic agent ammonium chloride was used. Sertoli cells were seeded in serum-free defined medium at a density of 3 x 10(6) cells/0.64-cm2 well on Matrigel-covered Millicell-HA filters. Chloroquine at concentrations ranging from 25 to 100 microM was added to the outer chamber of the bicameral system on either day 1 or 7 of the culture. The formation of the tight junction was monitored by the measurement of the transepithelial resistance (TER) at 24-hour intervals using an impedance meter. TER in untreated controls was 50 ohms/cm2 on day 1; it increased progressively to 80 ohms/cm2 by day 7 and plateaued until day 12. The cells treated from day 1 with chloroquine also showed a dose-dependent progressive increase in TER until day 9, reaching 225 ohms/cm2 in cells treated with the 100 microM concentration. In comparison to controls, the increase in TER was significantly higher. In cells treated with chloroquine starting from day 7 of culture onwards, there was no observable difference in TER from the untreated control. These observations demonstrate that chloroquine and ammonium chloride increase the TER of immature Sertoli cells in the bicameral chamber.

摘要

生精上皮中相邻的未成熟支持细胞形成紧密连接复合体,导致血睾屏障的发育。蛋白酶和抗蛋白酶活性与紧密连接的形成过程有关。在此,我们报告氯喹(一种具有抗蛋白酶活性的抗疟药物)对培养的未成熟大鼠支持细胞间紧密连接发育的影响。作为阳性对照,使用了经典的溶酶体促渗剂氯化铵。将支持细胞以3×10⁶个细胞/0.64平方厘米孔的密度接种在覆盖有基质胶的Millicell-HA滤器上的无血清限定培养基中。在培养的第1天或第7天,将浓度范围为25至100微摩尔的氯喹添加到双室系统的外室中。使用阻抗仪每隔24小时测量跨上皮电阻(TER)来监测紧密连接的形成。未处理的对照在第1天的TER为50欧姆/平方厘米;到第7天逐渐增加到80欧姆/平方厘米,并在第12天之前保持稳定。从第1天开始用氯喹处理的细胞,其TER也呈剂量依赖性逐渐增加,直到第9天,用100微摩尔浓度处理的细胞达到225欧姆/平方厘米。与对照相比,TER的增加明显更高。从培养第7天开始用氯喹处理的细胞,其TER与未处理的对照没有可观察到的差异。这些观察结果表明,氯喹和氯化铵增加了双室培养中未成熟支持细胞的TER。

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