Bernardini Chiara, La Mantia Debora, Salaroli Roberta, Zannoni Augusta, Nauwelaerts Nina, Deferm Neel, Ventrella Domenico, Bacci Maria Laura, Sarli Giuseppe, Bouisset-Leonard Michele, Annaert Pieter, Forni Monica
Department of Veterinary Medical Sciences, University of Bologna, Ozzano dell'Emilia, 40064 Bologna, Italy.
Health Sciences and Technologies-Interdepartmental Center for Industrial Research (CIRI-SDV), Alma Mater Studiorum-University of Bologna, 40126 Bologna, Italy.
Animals (Basel). 2021 Jul 5;11(7):2012. doi: 10.3390/ani11072012.
The ConcePTION project aims at generating further knowledge about the risks related to the use of medication during breastfeeding, as this information is lacking for most commonly used drugs. Taking into consideration multiple aspects, the pig model has been considered by the consortium as the most appropriate choice. The present research was planned to develop an efficient method for the isolation and culture of porcine Mammary Epithelial Cells (pMECs) to study the mammary epithelial barrier in vitro. Mammary gland tissues were collected at a local slaughterhouse, dissociated and the selected cellular population was cultured, expanded and characterized by morphology, cell cycle analysis and immunophenotyping. Their ability to create a barrier was tested by TEER measurement and sodium fluorescein transport activity. Expression of 84 genes related to drug transporters was evaluated by a PCR array. Our results show that primary cells express epithelial cell markers: CKs, CK18, E-Cad and tight junctions molecules ZO-1 and OCL. All the three pMEC cellular lines were able to create a tight barrier, although with different strengths and kinetics, and express the main ABC and SLC drug transporters. In conclusion, in the present paper we have reported an efficient method to obtain primary pMEC lines to study epithelial barrier function in the pig model.
“概念”项目旨在获取更多关于母乳喂养期间用药风险的知识,因为大多数常用药物都缺乏此类信息。考虑到多个方面,该联盟认为猪模型是最合适的选择。本研究旨在开发一种高效的方法,用于分离和培养猪乳腺上皮细胞(pMECs),以便在体外研究乳腺上皮屏障。在当地屠宰场收集乳腺组织,进行解离,然后对所选细胞群体进行培养、扩增,并通过形态学、细胞周期分析和免疫表型分析进行表征。通过跨上皮电阻(TEER)测量和荧光素钠转运活性测试它们形成屏障的能力。通过PCR阵列评估84个与药物转运体相关基因的表达。我们的结果表明,原代细胞表达上皮细胞标志物:细胞角蛋白(CKs)、CK18、E-钙黏蛋白(E-Cad)以及紧密连接分子闭合蛋白1(ZO-1)和紧密连接蛋白(OCL)。所有三种pMEC细胞系都能够形成紧密屏障,尽管强度和动力学有所不同,并且表达主要的ATP结合盒(ABC)和溶质载体(SLC)药物转运体。总之,在本文中我们报告了一种高效的方法,可获得原代pMEC细胞系,用于在猪模型中研究上皮屏障功能。