TY - JOUR
T1 - Microphysiologic systems in female reproductive biology
AU - Young, Alexandria N.
AU - Moyle-Heyrman, Georgette
AU - Kim, J. Julie
AU - Burdette, Joanna E.
N1 - Funding Information:
The authors wish to acknowledge financial support through grant UH3 TR001207 from the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Bethesda, Maryland.
Publisher Copyright:
© 2017, © 2017 by the Society for Experimental Biology and Medicine.
PY - 2017/11/1
Y1 - 2017/11/1
N2 - Microphysiologic systems (MPS), including new organ-on-a-chip technologies, recapitulate tissue microenvironments by employing specially designed tissue or cell culturing techniques and microfluidic flow. Such systems are designed to incorporate physiologic factors that conventional 2D or even 3D systems cannot, such as the multicellular dynamics of a tissue–tissue interface or physical forces like fluid sheer stress. The female reproductive system is a series of interconnected organs that are necessary to produce eggs, support embryo development and female health, and impact the functioning of non-reproductive tissues throughout the body. Despite its importance, the human reproductive tract has received less attention than other organ systems, such as the liver and kidney, in terms of modeling with MPS. In this review, we discuss current gaps in the field and areas for technological advancement through the application of MPS. We explore current MPS research in female reproductive biology, including fertilization, pregnancy, and female reproductive tract diseases, with a focus on their clinical applications. Impact statement: This review discusses existing microphysiologic systems technology that may be applied to study of the female reproductive tract, and those currently in development to specifically investigate gametes, fertilization, embryo development, pregnancy, and diseases of the female reproductive tract. We focus on the clinical applicability of these new technologies in fields such as assisted reproductive technologies, drug testing, disease diagnostics, and personalized medicine.
AB - Microphysiologic systems (MPS), including new organ-on-a-chip technologies, recapitulate tissue microenvironments by employing specially designed tissue or cell culturing techniques and microfluidic flow. Such systems are designed to incorporate physiologic factors that conventional 2D or even 3D systems cannot, such as the multicellular dynamics of a tissue–tissue interface or physical forces like fluid sheer stress. The female reproductive system is a series of interconnected organs that are necessary to produce eggs, support embryo development and female health, and impact the functioning of non-reproductive tissues throughout the body. Despite its importance, the human reproductive tract has received less attention than other organ systems, such as the liver and kidney, in terms of modeling with MPS. In this review, we discuss current gaps in the field and areas for technological advancement through the application of MPS. We explore current MPS research in female reproductive biology, including fertilization, pregnancy, and female reproductive tract diseases, with a focus on their clinical applications. Impact statement: This review discusses existing microphysiologic systems technology that may be applied to study of the female reproductive tract, and those currently in development to specifically investigate gametes, fertilization, embryo development, pregnancy, and diseases of the female reproductive tract. We focus on the clinical applicability of these new technologies in fields such as assisted reproductive technologies, drug testing, disease diagnostics, and personalized medicine.
KW - Microphysiologic systems
KW - female reproductive tract
KW - microfluidic systems
KW - organ on a chip
KW - personalized medicine
KW - reproductive biology
UR - http://www.scopus.com/inward/record.url?scp=85032354690&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85032354690&partnerID=8YFLogxK
U2 - 10.1177/1535370217697386
DO - 10.1177/1535370217697386
M3 - Review article
C2 - 29065798
AN - SCOPUS:85032354690
SN - 1535-3702
VL - 242
SP - 1690
EP - 1700
JO - Experimental Biology and Medicine
JF - Experimental Biology and Medicine
IS - 17
ER -