Author
Listed:
- Monica M. Laronda
(Feinberg School of Medicine, Northwestern University
Center for Reproductive Science, Northwestern University
Oncofertility Consortium, Northwestern University)
- Alexandra L. Rutz
(Simpson Querrey Institute for BioNanotechnology, Northwestern University
Northwestern University)
- Shuo Xiao
(Feinberg School of Medicine, Northwestern University
Center for Reproductive Science, Northwestern University
Oncofertility Consortium, Northwestern University)
- Kelly A. Whelan
(Feinberg School of Medicine, Northwestern University
Center for Reproductive Science, Northwestern University
Oncofertility Consortium, Northwestern University)
- Francesca E. Duncan
(Feinberg School of Medicine, Northwestern University
Center for Reproductive Science, Northwestern University
Oncofertility Consortium, Northwestern University
University of Kansas Medical Center)
- Eric W. Roth
(Northwestern University Atomic and Nanoscale Characterization Experimental Center, Northwestern University)
- Teresa K. Woodruff
(Feinberg School of Medicine, Northwestern University
Center for Reproductive Science, Northwestern University
Oncofertility Consortium, Northwestern University)
- Ramille N. Shah
(Simpson Querrey Institute for BioNanotechnology, Northwestern University
Northwestern University
Northwestern University
Feinberg School of Medicine, Northwestern University)
Abstract
Emerging additive manufacturing techniques enable investigation of the effects of pore geometry on cell behavior and function. Here, we 3D print microporous hydrogel scaffolds to test how varying pore geometry, accomplished by manipulating the advancing angle between printed layers, affects the survival of ovarian follicles. 30° and 60° scaffolds provide corners that surround follicles on multiple sides while 90° scaffolds have an open porosity that limits follicle–scaffold interaction. As the amount of scaffold interaction increases, follicle spreading is limited and survival increases. Follicle-seeded scaffolds become highly vascularized and ovarian function is fully restored when implanted in surgically sterilized mice. Moreover, pups are born through natural mating and thrive through maternal lactation. These findings present an in vivo functional ovarian implant designed with 3D printing, and indicate that scaffold pore architecture is a critical variable in additively manufactured scaffold design for functional tissue engineering.
Suggested Citation
Monica M. Laronda & Alexandra L. Rutz & Shuo Xiao & Kelly A. Whelan & Francesca E. Duncan & Eric W. Roth & Teresa K. Woodruff & Ramille N. Shah, 2017.
"A bioprosthetic ovary created using 3D printed microporous scaffolds restores ovarian function in sterilized mice,"
Nature Communications, Nature, vol. 8(1), pages 1-10, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15261
DOI: 10.1038/ncomms15261
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