首页> 外文期刊>Biochemistry and Cell Biology >Drug resistance is affected by colocalization of P-glycoproteins in raft-like structures unexpected in eggshells of the nematode Haemonchus contortus.
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Drug resistance is affected by colocalization of P-glycoproteins in raft-like structures unexpected in eggshells of the nematode Haemonchus contortus.

机译:耐药性受线虫Haemonchus contortus卵壳中意外的筏状结构中P-糖蛋白共定位的影响。

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摘要

In nematodes as in other eukaryotes, there is increasing evidence that drug resistance depends on both changes in the drug cellular targets and in nonspecific mechanisms, involving cellular detoxification by efflux pumps. In vertebrates, P-glycoproteins (Pgp) are membrane efflux pumps responsible for the elimination of xenobiotic agents, especially drugs. We previously reported the presence of Pgp pumps in eggshells and cuticles of the nematode Haemonchus contortus. Eggshells and cuticles are different from cell membranes, in particular they include a chitin layer. Nevertheless these structures present some common biological features with cell membranes and play a role in xenobiotic transport. Pgp activity has been shown to depend on the lipid environment and, in particular, on the cholesterol content in both vertebrate and nematode models. In vertebrates, Pgp is in part located in membrane cholesterol-enriched microdomains, the rafts. We describe here, for the first time, lipid microdomains in eggshells that could correspond with raft-like structures (RLSs). Moreover, a large proportion of the Pgp was shown to colocalize with these RLSs. The functional consequences of the colocalization for xenobiotic transport and thus drug resistance in nematodes were analyzed and compared with results obtained in vertebrates. An understanding of such mechanisms is crucial in overcoming the failure of drug treatments due to the development of resistance.
机译:与其他真核生物一样,在线虫中,越来越多的证据表明耐药性既取决于药物细胞靶标的变化,也取决于非特异性机制的变化,包括外排泵对细胞的​​排毒作用。在脊椎动物中,P-糖蛋白(Pgp)是膜外排泵,负责消除异种药物,尤其是药物。我们先前曾报道过线虫Haemonchus contortus的蛋壳和角质层中存在Pgp泵。蛋壳和角质层与细胞膜不同,特别是它们包括几丁质层。然而,这些结构在细胞膜上表现出一些共同的生物学特征,并在异源生物运输中起作用。已经显示出Pgp活性取决于脂质环境,尤其取决于脊椎动物和线虫模型中的胆固醇含量。在脊椎动物中,Pgp部分位于富含膜胆固醇的微区中,即筏子中。我们在这里首次描述了可能与筏状结构(RLSs)相对应的蛋壳中的脂质微区。此外,大部分Pgp与这些RLS共定位。分析了共定位对异种生物运输的功能后果,从而分析了线虫的耐药性,并将其与在脊椎动物中获得的结果进行了比较。对这种机制的理解对于克服由于耐药性的发展而导致药物治疗失败至关重要。

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