Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Drug Delivery and Disposition Lab, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, O&N II Herestraat 49-Bus 921, 3000 Leuven, Belgium.
Int J Mol Sci. 2024 Oct 25;25(21):11454. doi: 10.3390/ijms252111454.
It is currently impossible to perform an evidence-based risk assessment for medication use during breastfeeding. The ConcePTION project aims to provide information about the use of medicines during lactation. The study aimed to develop and characterize an in vitro model of the blood-milk barrier to determine the extent of the milk transfer of xenobiotics, relying on either on human mammary epithelial cells (hMECs) or immortalized cell lines derived from breast tissue. The hMECs were cultured and characterized for epithelial markers; further, the ability to form an epithelial barrier was investigated. Drug transporter functionality in the cultured hMECs was analyzed with specific probe substrates. The hMECs showed an epithelial morphology and the expression of epithelial markers and tight junctions. They formed a reproducible tight barrier with a transepithelial electrical resistance greater than 400 Ωcm, unlike immortalized cell lines. Different levels of mRNA expression were detected for 81 genes of membrane transporters. Functional assays showed no evidence for the transporter-mediated secretion of medicines across the hMECs. Nevertheless, the hMEC-based in vitro model covered a 50-fold range of permeability values, differentiating between passive transcellular and paracellular-mediated transport. The cultured hMECs proved to be a promising in vitro model for biorelevance; the wide characterization of hMECs makes them useful for studying medicine partitioning in milk.
目前,对于母乳喂养期间药物使用进行基于证据的风险评估是不可能的。 ConcePTION 项目旨在提供哺乳期用药信息。该研究旨在开发和表征血乳屏障的体外模型,以确定外源性物质通过乳汁的转移程度,该模型依赖于人乳腺上皮细胞(hMEC)或源自乳腺组织的永生化细胞系。hMEC 被培养和表型标志物进行了特征分析;此外,还研究了形成上皮屏障的能力。用特定的探针底物分析了培养的 hMEC 中的药物转运蛋白功能。hMEC 呈现出上皮形态和上皮标志物及紧密连接的表达。与永生化细胞系不同,它们形成了一种具有大于 400 Ωcm 的可重复紧密屏障的紧密屏障。检测到 81 个膜转运蛋白基因的 mRNA 表达水平不同。功能测定表明,hMEC 不具有跨 hMEC 分泌药物的转运体介导作用。尽管如此,基于 hMEC 的体外模型涵盖了 50 倍的通透性值范围,区分了被动跨细胞和细胞旁介导的转运。培养的 hMEC 被证明是一种有前途的生物相关性体外模型;hMEC 的广泛特征分析使其成为研究药物在乳中分配的有用工具。