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The case for applying tissue engineering methodologies to instruct human organoid morphogenesis.

Carlos R Marti-Figueroa1, Randolph S Ashton1

  • 1Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53706, United States; Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI 53715, United States.

Acta Biomaterialia
|March 20, 2017
PubMed
Summary
This summary is machine-generated.

Tissue engineering can guide human pluripotent stem cell (hPSC)-derived organoid development. This approach aims to create standardized, biomimetic 3D organoids for research and potential transplantation.

Keywords:
3-D printingBioprintingClick chemistryHydrogelsMorphogen gradientsOrganoid morphogenesisPhotochemistrySacrificial moldingTissue cytoarchitectureTissue morphology

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Area of Science:

  • Biomedical Engineering
  • Developmental Biology
  • Stem Cell Biology

Background:

  • Human pluripotent stem cell (hPSC)-derived 3D organoids offer biomimetic in vitro models for studying development and disease.
  • Current organoid protocols rely on spontaneous morphogenesis, leading to macroscale inconsistencies in morphology, cytoarchitecture, and cellular composition.
  • These limitations hinder the standardization and application of organoids for research and potential therapeutic uses.

Purpose of the Study:

  • To review tissue engineering methodologies for instructing multiscale, 3D organoid morphogenesis.
  • To explore how integrating tissue engineering with organoid derivation can overcome current limitations.
  • To harness organoid morphogenesis for engineering functional human tissues with biomimetic anatomy and physiology.

Main Methods:

  • Review of existing tissue engineering strategies applicable to organoid development.
  • Discussion of methods to control microscale morphogenesis for macroscale biomimicry.
  • Exploration of technological mergers between tissue engineering and organoid derivation protocols.

Main Results:

  • Tissue engineering approaches offer potential for precise control over organoid morphogenesis at multiple scales.
  • Standardized in vitro morphogenesis can yield organoids with improved biomimicry in morphology, cytoarchitecture, and cellular composition.
  • This integration is crucial for advancing organoid technology towards functional tissue engineering.

Conclusions:

  • Integrating tissue engineering with hPSC-derived organoid protocols is essential for achieving controlled, biomimetic morphogenesis.
  • This synergy will enable the development of 'next-generation' organoids for advanced research and potential organ transplantation.
  • Harnessing these methodologies will unlock the full potential of organoids in creating anatomically correct and physiologically relevant human tissue models.