Abstract

Organoid technology holds great promise for regenerative medicine. Recent studies show feasibility for bile duct tissue repair in humans by successfully transplanting cholangiocyte organoids in liver grafts during perfusion. Large-scale expansion of cholangiocytes is essential for extending these regenerative medicine applications. Human cholangiocyte organoids have a high and stable proliferation capacity, making them an attractive source of cholangiocytes. Commercially available basement membrane extract (BME) is used to expand the organoids. BME allows the cells to self-organize into 3D structures and stimulates cell proliferation. However, the use of BME is limiting the clinical applications of the organoids. There is a need for alternative tissue-specific and clinically relevant culture substrates capable of supporting organoid proliferation. Hydrogels prepared from decellularized and solubilized native livers are an attractive alternative for BME. These hydrogels can be used for the culture and expansion of cholangiocyte organoids in a clinically relevant manner. Moreover, the liver-derived hydrogels retain tissue-specific aspects of the extracellular microenvironment. They are composed of a complex mixture of bioactive and biodegradable extracellular matrix (ECM) components and can support the growth of various hepatobiliary cells. In this review, we provide an overview of the clinical potential of native liver ECM-based hydrogels for applications with human cholangiocyte organoids. We discuss the current limitations of BME for the clinical applications of organoids and how native ECM hydrogels can potentially overcome these problems in an effort to unlock the full regenerative clinical potential of the organoids.

Highlights

  • The aim of this review is to discuss the potential of native human liver extracellular matrix (ECM) for the clinical grade applications of cholangiocyte organoids for regenerative medicine in patients

  • Cholangiocyte organoids can be initiated from liver tissue biopsies different sources of organoids

  • Giobbe et al showed that different endodermal organoids can be cultured in non-tissue-specific ECM-derived hydrogels derived from decellularized porcine small intestinal submucosa (SIS) [119]

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Summary

Introduction with regard to jurisdictional claims in

The shortage of donor organs is a central theme in the field of liver transplantation, which still is the only curative treatment option for patients suffering from end-stage liver failure. Cholangiocytes form an active barrier between the cytotoxic bile and surrounding tissue [7] They are sensitive to ischemia, and the extra period of warm ischemia in DCD transplantation can cause deficits in the biliary epithelium, such as non-anastomotic strictures [4,8,9]. Eshmuminov et al recently showed that it is feasible to maintain human livers on the pump for up to 7 days [10] These improvements in the field of organ preservation could open up a window of opportunity for ex vivo organ repair. The aim of this review is to discuss the potential of native human liver extracellular matrix (ECM) for the clinical grade applications of cholangiocyte organoids for regenerative medicine in patients. We will discuss how liver ECM hydrogels provide an alternative culture substrate and why the use of decellularized liver tissue can unlock the full clinical potential of cholangiocyte organoids

The Potential of Organoids in Tissue Regeneration
Schematic
Repairing
Basement Membrane Extract as Culture Substrates
Tissue-Specific Alternative Culture Substrates
Hydrogels as an ECM Mimic
ECM-Based Hydrogels
Applications of Liver ECM Extracts
Finding a Suitable Source of Liver ECM
Unlocking the Future Clinical Potential of Cholangiocyte Organoids
Tissue Engineering the Biliary Tree
Potential
Findings
Summary
Full Text
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