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有机阴离子转运多肽1B1和1B3蛋白在小儿肝脏中的表达模式

Expression Patterns of Organic Anion Transporting Polypeptides 1B1 and 1B3 Protein in Human Pediatric Liver.

作者信息

Thomson Margaret M S, Hines Ronald N, Schuetz Erin G, Meibohm Bernd

机构信息

Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee (M.M.S.T., B.M.); Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin (R.N.H.); and Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital Memphis, Tennessee (E.G.S.).

Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee (M.M.S.T., B.M.); Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin (R.N.H.); and Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital Memphis, Tennessee (E.G.S.)

出版信息

Drug Metab Dispos. 2016 Jul;44(7):999-1004. doi: 10.1124/dmd.115.069252. Epub 2016 Apr 20.

Abstract

Determining appropriate pharmacotherapy in young children can be challenging due to uncertainties in the development of drug disposition pathways. With knowledge of the ontogeny of drug-metabolizing enzymes and an emerging focus on drug transporters, the developmental pattern of the uptake transporters organic anion transporting polypeptide (OATP) 1B1 and 1B3 was assessed by relative protein quantification using Western blotting in 80 human pediatric liver specimens covering an age range from 9 days to 12 years. OATP1B3 exhibited high expression at birth, which declined over the first months of life, and then increased again in the preadolescent period. In comparison with children 6-12 years of age, the relative protein expression of highly glycosylated (total) OATP1B3 was 235% (357%) in children <3 months of age, 33% (64%) in the age group from 3 months to 2 years, and 50% (59%) in children 2-6 years of age. The fraction of highly glycosylated to total OATP1B3 increased with age, indicating ontogenic processes not only at the transcriptional level but also at the post-translational level. Similar to OATP1B3, OATP1B1 showed high interindividual variability in relative protein expression but no statistically significant difference among the studied age groups.

摘要

由于药物处置途径发育的不确定性,确定年幼儿童的适当药物治疗可能具有挑战性。随着对药物代谢酶个体发生的了解以及对药物转运体的日益关注,通过蛋白质免疫印迹法对相对蛋白质进行定量,评估了80份覆盖9天至12岁年龄范围的人类儿科肝脏标本中摄取转运体有机阴离子转运多肽(OATP)1B1和1B3的发育模式。OATP1B3在出生时表达较高,在生命的最初几个月下降,然后在青春期前再次增加。与6至12岁儿童相比,高度糖基化(总)OATP1B3的相对蛋白表达在3个月龄以下儿童中为235%(357%),在3个月至2岁年龄组中为33%(64%),在2至6岁儿童中为50%(59%)。高度糖基化的OATP1B3占总OATP1B3的比例随年龄增加,表明不仅在转录水平而且在翻译后水平都存在个体发育过程。与OATP1B3相似,OATP1B1在相对蛋白表达上表现出较高的个体间变异性,但在所研究的年龄组之间没有统计学上的显著差异。

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