Abstract

The biliary tree is an essential component of transplantable human liver tissue. Despite recent advances in liver tissue engineering, attempts at re-creating the intrahepatic biliary tree have not progressed significantly. The finer branches of the biliary tree are structurally and functionally complex and heterogeneous and require harnessing innate developmental processes for their regrowth. Here we demonstrate the ability of decellularized liver extracellular matrix (dECM) hydrogels to induce the in vitro formation of complex biliary networks using encapsulated immortalized mouse small biliary epithelial cells (cholangiocytes). This phenomenon is not observed using immortalized mouse large cholangiocytes, or with purified collagen 1 gels or Matrigel. We also show phenotypic stability via immunostaining for specific cholangiocyte markers. Moreover, tight junction formation and maturation was observed to occur between cholangiocytes, exhibiting polarization and transporter activity. To better define the mechanism of duct formation, we utilized three fluorescently labeled, but otherwise identical populations of cholangiocytes. The cells, in a proximity dependent manner, either branch out clonally, radiating from a single nucleation point, or assemble into multi-colored structures arising from separate populations. These findings present liver dECM as a promising biomaterial for intrahepatic bile duct tissue engineering and as a tool to study duct remodeling in vitro.

Details

Title
Complex bile duct network formation within liver decellularized extracellular matrix hydrogels
Author
Lewis, Phillip L. 1 ; Su, Jimmy 1   VIAFID ORCID Logo  ; Yan, Ming 1 ; Meng, Fanyin 2 ; Glaser, Shannon S. 3 ; Alpini, Gianfranco D. 3 ; Green, Richard M. 4 ; Sosa-Pineda, Beatriz 5 ; Shah, Ramille N. 6 

 Biomedical Engineering, Northwestern University, Evanston, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Simpson Querrey Institute, Northwestern University, Chicago, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Research Central Texas Veterans Health Care System, Temple, TX, USA (GRID:grid.413775.3) (ISNI:0000 0004 0420 5847); Baylor Scott & White Health Digestive Disease Research Center, Temple, TX, USA (GRID:grid.486749.0) (ISNI:0000 0004 4685 2620) 
 Research Central Texas Veterans Health Care System, Temple, TX, USA (GRID:grid.413775.3) (ISNI:0000 0004 0420 5847); Baylor Scott & White Health Digestive Disease Research Center, Temple, TX, USA (GRID:grid.486749.0) (ISNI:0000 0004 4685 2620); Medical Physiology, Texas A&M University College of Medicine, Temple, TX, USA (GRID:grid.264756.4) (ISNI:0000 0004 4687 2082) 
 Division of Gastroenterology and Hepatology, Northwestern University, Chicago, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Nephrology, Northwestern University, Chicago, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Simpson Querrey Institute, Northwestern University, Chicago, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Materials Science and Engineering, Northwestern University, Evanston, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Surgery (Transplant Division), Northwestern University, Chicago, IL, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
Pages
12220
Publication year
2018
Publication date
2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2766281245
Copyright
© The Author(s) 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.