4.7 Article

Complex bile duct network formation within liver decellularized extracellular matrix hydrogels

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SCIENTIFIC REPORTS
卷 8, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-018-30433-6

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资金

  1. NCI CCSG [P30 CA060553]
  2. U.S. Army Research Office
  3. U.S. Army Medical Research and Materiel Command
  4. Northwestern University
  5. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF NNCI-1542205]
  6. Northwestern University -Flow Cytometry Core Facility
  7. Cancer Center Support Grant [NCI CA060553]
  8. NIH [1S10OD011996-01, DK076898]
  9. National Institutes of Health [1K01DK099454]
  10. Primary Sclerosing Cholangitis (PSC) Partners Seeking a Cure grant [7280909288FF]
  11. Northwestern University's Biotechnology Training Program Cluster Award
  12. National Institutes of Health Predoctoral Biotechnology Training Program [NIGMS T32 GM008449]
  13. Ruth L. Kirschstein National Research Service Award Individual Predoctoral Fellowship [NRSA F31 NIDDK 1F31DK108544-01A1]
  14. Dr. Nicholas C. Hightower Centennial Chair of Gastroenterology from Scott White
  15. VA Research Career Scientist Award from the United States (U.S.) Department of Veterans Affairs Biomedical Laboratory Research and Development Service
  16. VA Merit Award from the United States (U.S.) Department of Veterans Affairs Biomedical Laboratory Research and Development Service [1I01BX001724, 5I01BX000574, 5I01BX002192]

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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.

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