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用于确定牛磺胆酸盐在三明治培养大鼠肝细胞中肝胆处置的培养条件优化

Optimization of culture conditions for determining hepatobiliary disposition of taurocholate in sandwich-cultured rat hepatocytes.

作者信息

Chandra P, Lecluyse E L, Brouwer K L

机构信息

Division of Drug Delivery and Disposition, University of North Carolina at Chapel Hill, 27599, USA.

出版信息

In Vitro Cell Dev Biol Anim. 2001 Jun;37(6):380-5. doi: 10.1007/BF02577575.

Abstract

This study was undertaken to examine the influence of time and volume of collagen overlay, type of media, and media additives on taurocholate (TC) accumulation and biliary excretion in hepatocytes cultured in a collagen-sandwich configuration. Hepatocytes were isolated from male Wistar rats by in situ perfusion with collagenase, seeded onto collagen-coated 60-mm dishes, overlaid with gelled collagen, and cultured for 4 d. Experiments to examine the influence of time and volume of collagen overlay were conducted in Dulbecco's modified Eagle's medium (DMEM) + 1.0 microM dexamethasone (DEX) + 5% fetal bovine serum (FBS). Hepatocytes were overlaid at 0 h with 0.1 or 0.2 ml collagen, or at 24 h with 0.1 or 0.2 ml collagen. The influence of media type and additives was examined in hepatocytes overlaid at 0 h with 0.2 ml collagen and incubated in DMEM + 0.1 microM DEX, DMEM +/- 0.1 microM DEX + 5% FBS, Williams' medium E + 0.1 microM DEX + 1% ITS+, DMEM + 1.0 microM DEX, DMEM + 1.0 microM DEX + 5% FBS, or modified Chee's medium (MCM) + 0.1 microM DEX + 1% ITS+. [3H] TC accumulation by hepatocytes in Hank's balanced salt solution (HBSS) and Ca2+-free HBSS was measured, and the biliary-exeretion index (BEI: percentage of accumulated TC localized in the canalicular compartment) was calculated. Light microscopy and carboxydichlorofluorescein fluorescence were employed to examine the cellular and canalicular morphologies. The volume of collagen used for both the substratum and the overlay did not affect TC accumulation or biliary excretion. The BEI tended to be higher in cells overlaid at 24 h (BEI = 0.649 [0.1 ml collagen]; BEI = 0.659 [0.2 ml collagen]) compared with those overlaid at 0 h after seeding (BEI = 0.538 [0.1 ml collagen]; BEI = 0.517 [0.2 ml collagen]), although the differences were not statistically significant. Hepatocytes cultured in MCM produced consistently the lowest BEI of TC (BEI = 0.396). Differing DEX concentrations (0.1 microM versus 1.0 microM) with or without 5% FBS did not appear to have a significant effect on the BEI of TC.

摘要

本研究旨在探讨胶原蛋白覆盖的时间和体积、培养基类型以及培养基添加剂对以胶原蛋白夹心结构培养的肝细胞中牛磺胆酸盐(TC)积累和胆汁排泄的影响。通过用胶原酶原位灌注从雄性Wistar大鼠分离肝细胞,接种到胶原包被的60毫米培养皿上,覆盖凝胶化的胶原蛋白,并培养4天。在杜尔贝科改良伊格尔培养基(DMEM)+1.0微摩尔地塞米松(DEX)+5%胎牛血清(FBS)中进行实验,以研究胶原蛋白覆盖时间和体积的影响。肝细胞在0小时时用0.1或0.2毫升胶原蛋白覆盖,或在24小时时用0.1或0.2毫升胶原蛋白覆盖。在0小时时用0.2毫升胶原蛋白覆盖并在DMEM +0.1微摩尔DEX、DMEM +/-0.1微摩尔DEX +5%FBS、威廉姆斯培养基E +0.1微摩尔DEX +1%ITS +、DMEM +1.0微摩尔DEX、DMEM +1.0微摩尔DEX +5%FBS或改良Chee培养基(MCM)+0.1微摩尔DEX +1%ITS +中孵育的肝细胞中研究培养基类型和添加剂的影响。测量肝细胞在汉克平衡盐溶液(HBSS)和无钙HBSS中[3H]TC的积累,并计算胆汁排泄指数(BEI:积累的TC定位于胆小管区室的百分比)。采用光学显微镜和羧基二氯荧光素荧光检查细胞和胆小管形态。用于底层和覆盖层的胶原蛋白体积均不影响TC积累或胆汁排泄。与接种后0小时覆盖的细胞(BEI =0.538 [0.1毫升胶原蛋白];BEI =0.517 [0.2毫升胶原蛋白])相比,24小时覆盖的细胞中BEI倾向于更高(BEI =0.649 [0.1毫升胶原蛋白];BEI =0.659 [0.2毫升胶原蛋白]),尽管差异无统计学意义。在MCM中培养的肝细胞产生的TC的BEI始终最低(BEI =0.396)。有或没有5%FBS时不同的DEX浓度(0.1微摩尔对1.0微摩尔)似乎对TC的BEI没有显著影响。

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