Krishnamurthy P, Schuetz J D
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Annu Rev Pharmacol Toxicol. 2006;46:381-410. doi: 10.1146/annurev.pharmtox.46.120604.141238.
The protein variously named ABCG2/BCRP/MXR/ABCP is a recently described ATP-binding cassette (ABC) transporter originally identified by its ability to confer drug resistance that is independent of Mrp1 (multidrug-resistance protein 1) and Pgp (P-glycoprotein). Unlike Mrp1 and Pgp, ABCG2 is a half-transporter that must homodimerize to acquire transport activity. ABCG2 is found in a variety of stem cells and may protect them from exogenous and endogenous toxins. ABCG2 expression is upregulated under low-oxygen conditions, consistent with its high expression in tissues exposed to low-oxygen environments. ABCG2 interacts with heme and other porphyrins and protects cells and/or tissues from protoporphyrin accumulation under hypoxic conditions. Individuals who carry ABCG2 alleles that have impaired function may be more susceptible to porphyrin-induced toxicity. Abcg2 knock-out models have allowed in vivo studies of Abcg2 function in host and cellular defense. In combination with immunohistochemical analyses, these studies have revealed how ABCG2 influences the absorption, distribution, and excretion of drugs and cytotoxins.
这种有多种命名的蛋白质,即ABCG2/BCRP/MXR/ABCP,是一种最近被描述的ATP结合盒(ABC)转运蛋白,最初是因其具有赋予与Mrp1(多药耐药蛋白1)和Pgp(P-糖蛋白)无关的耐药性的能力而被鉴定出来的。与Mrp1和Pgp不同,ABCG2是一种半转运蛋白,必须形成同源二聚体才能获得转运活性。ABCG2存在于多种干细胞中,可能保护它们免受外源性和内源性毒素的侵害。在低氧条件下,ABCG2的表达会上调,这与其在暴露于低氧环境的组织中的高表达一致。ABCG2与血红素和其他卟啉相互作用,并在缺氧条件下保护细胞和/或组织免受原卟啉积累的影响。携带功能受损的ABCG2等位基因的个体可能更容易受到卟啉诱导的毒性作用。ABCG2基因敲除模型使得在体内研究ABCG2在宿主和细胞防御中的功能成为可能。结合免疫组织化学分析,这些研究揭示了ABCG2如何影响药物和细胞毒素的吸收、分布和排泄。