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A microfluidic culture model of the human reproductive tract and 28-day menstrual cycle.

Shuo XiaoJonathan R CoppetaHunter B RogersBrett C IsenbergJie ZhuSusan A OlalekanKelly E McKinnonDanijela DokicAlexandra S RashediDaniel J HaisenlederSaurabh S MalpaniChanel A Arnold-MurrayKuanwei ChenMingyang JiangLu BaiCatherine T NguyenJiyang ZhangMonica M LarondaThomas J HopeKruti P ManiarMary Ellen PavoneMichael J AvramElizabeth C SeftonSpiro GetsiosJoanna E BurdetteJ Julie KimJeffrey T BorensteinTeresa K Woodruff
Published in: Nature communications (2017)
The endocrine system dynamically controls tissue differentiation and homeostasis, but has not been studied using dynamic tissue culture paradigms. Here we show that a microfluidic system supports murine ovarian follicles to produce the human 28-day menstrual cycle hormone profile, which controls human female reproductive tract and peripheral tissue dynamics in single, dual and multiple unit microfluidic platforms (Solo-MFP, Duet-MFP and Quintet-MPF, respectively). These systems simulate the in vivo female reproductive tract and the endocrine loops between organ modules for the ovary, fallopian tube, uterus, cervix and liver, with a sustained circulating flow between all tissues. The reproductive tract tissues and peripheral organs integrated into a microfluidic platform, termed EVATAR, represents a powerful new in vitro tool that allows organ-organ integration of hormonal signalling as a phenocopy of menstrual cycle and pregnancy-like endocrine loops and has great potential to be used in drug discovery and toxicology studies.
Keyphrases
  • endothelial cells
  • high throughput
  • circulating tumor cells
  • single cell
  • drug discovery
  • induced pluripotent stem cells
  • gene expression
  • adipose tissue
  • pregnant women
  • insulin resistance
  • human health
  • solid state