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Related Concept Videos

Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...

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Updated: Jul 19, 2026

Tissue Engineering of the Intestine in a Murine Model
08:45

Tissue Engineering of the Intestine in a Murine Model

Published on: December 1, 2012

Tissue engineering of small intestine--current status.

Ashish Gupta1, Anupam Dixit, Kevin M Sales

  • 1Biomaterials and Tissue Engineering Centre, Academic Division of Surgery and Interventional Sciences, University College London, London NW3 2PF, United Kingdom.

Biomacromolecules
|October 10, 2006
PubMed
Summary

Tissue engineering offers a promising alternative for short bowel syndrome (SBS). Researchers are developing artificial intestines using stem cells and biodegradable materials to increase intestinal surface area for patients with intestinal failure.

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Area of Science:

  • Biomedical Engineering
  • Regenerative Medicine
  • Gastroenterology

Background:

  • Short bowel syndrome (SBS) presents significant morbidity and mortality, with current treatments like parenteral nutrition (PN) and transplantation having limitations.
  • PN is associated with sepsis and liver failure, while transplantation faces donor organ scarcity and graft rejection issues.
  • Existing therapeutic options for SBS are not permanent solutions, highlighting the need for alternative treatments.

Purpose of the Study:

  • To review the current progress in small intestinal tissue engineering.
  • To explore potential cell sources and scaffold materials for artificial intestine development.
  • To discuss the promise of tissue-engineered intestines as a novel therapy for SBS.

Main Methods:

  • Review of existing literature on small intestinal tissue engineering techniques.
  • Analysis of studies involving seeding of intestinal epithelial organoids onto biodegradable polymers.
  • Examination of advancements in cultured stem cell and polymer technologies.

Main Results:

  • Successful generation of intestinal neomucosa in animal models using seeded organoid units on biodegradable polymers.
  • Demonstration of potential for engineered intestinal tissue to increase absorptive surface area.
  • Identification of cultured stem cells and advanced polymer technology as key components for future development.

Conclusions:

  • Small intestinal tissue engineering holds significant promise for developing an 'off-the-shelf' artificial intestine.
  • Continued research in cell sources and scaffold materials is crucial for advancing this novel therapy.
  • Tissue-engineered intestines could offer a viable, potentially permanent solution for patients suffering from intestinal failure due to SBS.