Microphysiological systems of the placental barrier

被引:52
作者
Arumugasaamy, Navein [1 ]
Rock, Kylie D. [2 ]
Kuo, Che-Ying [3 ]
Bale, Tracy L. [2 ]
Fisher, John P. [4 ,5 ]
机构
[1] GlaxoSmithKline, Prot Cellular & Struct Sci, 1250 S Collegeville Rd, Collegeville, PA 19426 USA
[2] Univ Maryland, Sch Med, Dept Pharmacol, Baltimore, MD 21201 USA
[3] Formlabs, Mat Engn, Somerville, MA USA
[4] Univ Maryland, Ctr Engn Complex Tissues, College Pk, MD 20742 USA
[5] Univ Maryland, Fischell Dept Bioengn, 4102A Clark Hall,8278 Paint Branch Dr, College Pk, MD 20742 USA
关键词
Placental biology; Transport; Metabolism; Microphysiological; Bioreactor; Hydrogel; Organ on a chip; Bioprinting; LOADED POLYMERIC NANOPARTICLES; IN-VITRO SIMULATION; EXTRAVILLOUS TROPHOBLASTS; VILLOUS CYTOTROPHOBLAST; EXTRACELLULAR VESICLES; MEMBRANE TRANSPORTERS; ENDOCRINE FUNCTION; ENDOTHELIAL-CELLS; EXPRESSION; MODEL;
D O I
10.1016/j.addr.2020.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methods to evaluate maternal-fetal transport across the placental barrier have generally involved clinical observations after-the-fact, ex vivo perfused placenta studies, or in vitro Transwell assays. Given the ethical and technical limitations in these approaches, and the drive to understand fetal development through the lens of transport-induced injury, such as with the examples of thalidomide and Zika Virus, efforts to develop novel approaches to study these phenomena have expanded in recent years. Notably, within the past 10 years, placental barrier models have been developed using hydrogel, bioreactor, organ-on-a-chip, and bioprinting approaches. In this review, we discuss the biology of the placental barrier and endeavors to recapitulate this barrier in vitro using these approaches. We also provide analysis of current limitations to drug discovery in this context, and end with a future outlook. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 175
页数:15
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