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

Shuo Xiao(Northwestern University), Jonathan Coppeta(Draper Laboratory), Hunter B. Rogers(Northwestern University), Brett C. Isenberg(Draper Laboratory), Jie Zhu(Northwestern University), Susan Olalekan(Northwestern University), Kelly E. McKinnon(Northwestern University), Danijela Đokić(Northwestern University), Alexandra S. Rashedi(Northwestern University), Daniel J. Haisenleder(University of Virginia), Saurabh Malpani(Northwestern University), Chanel A. Arnold-Murray(Northwestern University), Kuan-Wei Chen(Northwestern University), Mingyang Jiang(Northwestern University), Lu Bai(Northwestern University), Catherine T. Nguyen(Northwestern University), Jiyang Zhang(Northwestern University), Monica M. Laronda(Northwestern University), Thomas J. Hope(Northwestern University), Kruti P. Maniar(Northwestern University), Mary Ellen Pavone(Northwestern University), Michael J. Avram(Northwestern University), Elizabeth C. Sefton(Northwestern University), Spiro Getsios(Northwestern University), Joanna E. Burdette(University of Illinois Chicago), Julie Kim(Northwestern University), Jeffrey T. Borenstein(Draper Laboratory), Teresa K. Woodruff(Northwestern University)
Nature Communications
March 28, 2017
Cited by 465Open Access
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Abstract

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.


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