Continuous Production of Highly Functional Vascularized Hepatobiliary Organoids from Human Pluripotent Stem Cells using a Scalable Microfluidic Platform

Author:

Abbasalizadeh Saeed1234,Babaee Sahab456,Kowsari‐Esfahan Reza2,Mazidi Zahra1,Shi Yichao5,Wainer Jake4,Cabral Joaquim M. S.3,Langer Robert45,Traverso Giovanni456,Baharvand Hossein17ORCID

Affiliation:

1. Department of Stem Cells and Developmental Biology Cell Science Research Center Royan Institute for Stem Cell Biology and Technology ACECR Tehran 16635‐148 Iran

2. Department of Cell Engineering Cell Science Research Center Royan Institute for Stem Cell Biology and Technology ACECR Tehran 16635‐148 Iran

3. Department of Bioengineering and iBB – Institute for Bioengineering and Biosciences Institute Superior Técnico Universidade de Lisboa 1049‐001 Lisboa Portugal

4. Department of Chemical Engineering and Koch Institute for Integrative Cancer Research Massachusetts Institute of Technology Cambridge MA 02139 USA

5. Department of Mechanical Engineering Massachusetts Institute of Technology Cambridge MA 02139 USA

6. Division of Gastroenterology Brigham and Women's Hospital Harvard Medical School Boston MA 02115 USA

7. Department of Developmental Biology School of Basic Sciences and Advanced Technologies in Biology University of Science and Culture Tehran 16635‐148 Iran

Abstract

Abstract“Organoid medicine” has rapidly progressed over the past decade as a new class of therapeutics with high functionality and complexity for addressing unmet medical needs such as effective treatment of patients suffering from chronic liver disease using liver organoids. Here, scalable and xeno‐free integrated differentiation platforms are established to generate hepatic progenitors, mesenchymal stromal cells, and endothelial cells using individual human pluripotent stem cell lines as starting cell types for vascularized liver organoids generation. A scalable microfluidic system is developed to continuously generate cells‐loaded microcapsules with self‐biodegradable 4‐arm‐PEG‐MMP1‐sensitive peptide hydrogel as shell material, to support cells proliferation, self‐condensation, and liver organoids generation through self‐organization. Self‐organized vascularized hepatobiliary organoids (VHOs) containing interconnected biliary networks and vascular structures are generated after optimizing the co‐culture conditions inside hydrogel microcapsules and transferring the organoids to 3D dynamic suspension culture for further maturation. The VHOs show key functional features similar to the fetal and adult liver tissue including the expression of liver‐specific marker genes, the ability to perform main liver metabolic functions, and inducing drug metabolism. The established platforms can be beneficial to the mass production of human liver organoids for liver organoid medicine and the development of safe, effective, and personalized drugs.

Funder

Academic Center for Education, Culture and Research

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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