IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v8y2017i1d10.1038_ncomms15261.html
   My bibliography  Save this article

A bioprosthetic ovary created using 3D printed microporous scaffolds restores ovarian function in sterilized mice

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
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms15261
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms15261?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Conghui Tian & Lingxiao Shen & Chenjia Gong & Yunxia Cao & Qinghua Shi & Gang Zhao, 2022. "Microencapsulation and nanowarming enables vitrification cryopreservation of mouse preantral follicles," Nature Communications, Nature, vol. 13(1), pages 1-16, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15261. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.