首页> 美国卫生研究院文献>Biochemical Journal >Effects of preincubation of primary monolayer cultures of rat hepatocytes with low- and high-density lipoproteins on the subsequent binding and metabolism of human low-density lipoprotein.
【2h】

Effects of preincubation of primary monolayer cultures of rat hepatocytes with low- and high-density lipoproteins on the subsequent binding and metabolism of human low-density lipoprotein.

机译:低密度脂蛋白和高密度脂蛋白对大鼠肝细胞原代单层培养物的预孵育对人低密度脂蛋白随后结合和代谢的影响。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

1. There are two distinct binding sites (Site 1 and Site 2) for human low-density lipoprotein (LDL) on rat hepatocytes in monolayer culture [Salter, Saxton & Brindley (1986) Biochem. J. 240, 549-557]. 2. Binding of 125I-LDL to Site 1, but not to Site 2, is up-regulated between 20 and 44 h in culture by preincubation of the cells with human high-density lipoprotein 3 (HDL3). 3. A similar preincubation with HDL2 had no significant effect on binding to either site. 4. Preincubation with human LDL led to a partial down-regulation of subsequent binding of 125I-LDL to Site 1. Since binding after incubation with LDL was measured at 37 degrees C, binding to Site 2 could not be distinguished from LDL that had been internalized by the cells. 5. Hepatocytes were shown to degrade 125I-LDL, resulting in the accumulation of [125I]iodotyrosine in the medium. Evidence was found that iodotyrosine may be further degraded by deiodinase produced by the cells. 6. Regulation of binding to Site 1 by preincubation with LDL or HDL3 was found to lead to a parallel regulation of LDL degradation. 7. It is concluded that rat hepatocytes not only bind but also metabolize human LDL and that these processes are under metabolic regulation.
机译:1.在单层培养中,大鼠肝细胞上的人类低密度脂蛋白(LDL)有两个不同的结合位点(位点1和位点2)[Salter,Saxton&Brindley(1986)Biochem。Chem。,第2期,第1期。 J. 240,549-557]。 2.通过将细胞与人高密度脂蛋白3(HDL3)预孵育,可在培养20到44 h之间将125I-LDL与位点1的结合而不是位点2的结合上调。 3.与HDL2的类似预温育对结合至任一位点均无明显影响。 4.与人LDL的预孵育导致125I-LDL与位点1的后续结合的部分下调。由于在37°C下测量了与LDL孵育后的结合,因此无法区分与位点2的结合。被细胞内在化。 5.显示肝细胞降解125I-LDL,导致[125I]碘酪氨酸在培养基中积累。有证据表明,碘酪氨酸可能会被细胞产生的脱碘酶进一步降解。 6.发现通过与LDL或HDL3预孵育来调节与位点1的结合导致平行调节LDL降解。 7.得出的结论是,大鼠肝细胞不仅会结合而且会代谢人LDL,并且这些过程处于代谢调节之下。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号