4.7 Article

A Bioprinted Tubular Intestine Model Using a Colon-Specific Extracellular Matrix Bioink

Journal

ADVANCED HEALTHCARE MATERIALS
Volume 11, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/adhm.202101768

Keywords

3D bioprinting; intestinal morphogenesis; material-guided cell maturation; tissue-specific bioinks; tubular intestine models

Funding

  1. MSIT (Ministry of Science and ICT), South Korea, under the ICT Creative Consilience program [IITP-2020-2011-1-00783]
  2. National Research Foundation of South Korea (NRF) - MSIT [2021R1A2C2004981, 2020R1A2B5B03002154]
  3. Leona M. & Harry B. Helmsley Charitable Trust [1912-03604]
  4. National Research Foundation of Korea [2021R1A2C2004981] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A physiologically relevant intestinal model with a 3D hollow tubular structure using 3D bioprinting strategy has been developed, utilizing colon-derived decellularized extracellular matrix as a tissue-specific biomaterial. Bioprinted intestinal tissue models demonstrate the spontaneous 3D morphogenesis of human intestinal epithelium, forming multicellular aggregates and cysts, and differentiating into various types of enterocytes, establishing junctional networks.
Tremendous advances have been made toward accurate recapitulation of the human intestinal system in vitro to understand its developmental process, and disease progression. However, current in vitro models are often confined to 2D or 2.5D microarchitectures, which is difficult to mimic the systemic level of complexity of the native tissue. To overcome this problem, physiologically relevant intestinal models are developed with a 3D hollow tubular structure using 3D bioprinting strategy. A tissue-specific biomaterial, colon-derived decellularized extracellular matrix (Colon dECM) is developed and it provides significant maturation-guiding potential to human intestinal cells. To fabricate a perfusable tubular model, a simultaneous printing process of multiple materials through concentrically assembled nozzles is developed and a light-activated Colon dECM bioink is employed by supplementing with ruthenium/sodium persulfate as a photoinitiator. The bioprinted intestinal tissue models show spontaneous 3D morphogenesis of the human intestinal epithelium without any external stimuli. In consequence, the printed cells form multicellular aggregates and cysts and then differentiate into several types of enterocytes, building junctional networks. This system can serve as a platform to evaluate the effects of potential drug-induced toxicity on the human intestinal tissue and create a coculture model with commensal microbes and immune cells for future therapeutics.

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