Age-Specific ADME Gene Expression in Infant Intestinal Enteroids.

IF 5.4 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
ACS Applied Energy Materials Pub Date : 2024-09-02 Epub Date: 2024-08-09 DOI:10.1021/acs.molpharmaceut.4c00302
Eva J Streekstra, Tom Scheer-Weijers, Michael Bscheider, Sabine Fuerst-Recktenwald, Adrian Roth, Sven C D van Ijzendoorn, Sanne Botden, Willem de Boode, Martijn W J Stommel, Rick Greupink, Frans G M Russel, Evita van de Steeg, Saskia N de Wildt
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Abstract

In childhood, developmental changes and environmental interactions highly affect orally dosed drug disposition across the age range. To optimize dosing regimens and ensure safe use of drugs in pediatric patients, understanding this age-dependent biology is necessary. In this proof-of-concept study, we aimed to culture age-specific enteroids from infant tissue which represent its original donor material, specifically for drug transport and metabolism. Enteroid lines from fresh infant tissues (n = 8, age range: 0.3-45 postnatal weeks) and adult tissues (n = 3) were established and expanded to 3D self-organizing enteroids. The gene expression of drug transporters P-gp (ABCB1), BCRP (ABCG2), MRP2 (ABCC2), and PEPT1 (SLC15A1) and drug metabolizing enzymes CYP3A4, CYP2C18, and UGT1A1 was determined with RT-qPCR in fresh tissue and its derivative differentiated enteroids. Expression levels of P-gp, BCRP, MRP2, and CYP3A4 were similar between tissues and enteroids. PEPT1 and CYP2C18 expression was lower in enteroids compared to that in the tissue. The expression of UGT1A1 in the tissue was lower than that in enteroids. The gene expression did not change with the enteroid passage number for all genes studied. Similar maturational patterns in tissues and enteroids were visually observed for P-gp, PEPT1, MRP2, CYP3A4, CYP2C18, and VIL1. In this explorative study, interpatient variability was high, likely due to the diverse patient characteristics of the sampled population (e.g., disease, age, and treatment). To summarize, maturational patterns of clinically relevant ADME genes in tissue were maintained in enteroids. These findings are an important step toward the potential use of pediatric enteroids in pediatric drug development, which in the future may lead to improved pediatric safety predictions during drug development. We reason that such an approach can contribute to a potential age-specific platform to study and predict drug exposure and intestinal safety in pediatrics.

Abstract Image

婴儿肠内 ADME 基因表达的年龄特异性
在儿童时期,发育变化和环境相互作用会对各年龄段口服药物的处置产生很大影响。为了优化给药方案,确保儿科患者安全用药,了解这种与年龄相关的生物学特性十分必要。在这项概念验证研究中,我们的目标是从婴儿组织中培养特定年龄的肠球菌,这些肠球菌代表了药物转运和代谢的原始供体材料。我们建立了来自新鲜婴儿组织(n = 8,年龄范围:出生后 0.3-45 周)和成人组织(n = 3)的肠球菌系,并将其扩增为三维自组织肠球菌。采用 RT-qPCR 方法测定了新鲜组织及其衍生物分化肠组织中药物转运体 P-gp (ABCB1)、BCRP (ABCG2)、MRP2 (ABCC2) 和 PEPT1 (SLC15A1) 以及药物代谢酶 CYP3A4、CYP2C18 和 UGT1A1 的基因表达。P-gp、BCRP、MRP2 和 CYP3A4 的表达水平在不同组织和肠组织中相似。与组织相比,PEPT1 和 CYP2C18 在肠组织中的表达较低。组织中 UGT1A1 的表达低于肠内。所研究的所有基因的表达量并不随肠球菌的通过数而变化。肉眼观察到 P-gp、PEPT1、MRP2、CYP3A4、CYP2C18 和 VIL1 在组织和肠道中的成熟模式相似。在这项探索性研究中,患者之间的差异很大,这可能是由于取样人群的患者特征各不相同(如疾病、年龄和治疗)。总之,组织中与临床相关的 ADME 基因的成熟模式在肠液中得以保持。这些发现是在儿科药物开发中潜在使用儿科肠道组织的重要一步,将来可能会改善药物开发过程中的儿科安全性预测。我们认为,这种方法有助于建立一个潜在的特定年龄平台,用于研究和预测儿科药物暴露和肠道安全性。
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来源期刊
ACS Applied Energy Materials
ACS Applied Energy Materials Materials Science-Materials Chemistry
CiteScore
10.30
自引率
6.20%
发文量
1368
期刊介绍: ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.
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