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An overview of post transplantation events of decellularized scaffolds. | LitMetric

An overview of post transplantation events of decellularized scaffolds.

Transpl Immunol

Tissue engineering lab, Anatomy Department, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address:

Published: October 2022

AI Article Synopsis

  • Regenerative medicine and tissue engineering offer potential alternatives to organ transplantation by using decellularized tissues for repairing damaged tissues.
  • The decellularization process retains key components of the extracellular matrix, creating 3D scaffolds that possess favorable mechanical properties and biocompatibility.
  • The review addresses post-transplantation events like cell migration, blood vessel formation (angiogenesis), and interactions with immune cells in decellularized scaffolds.

Article Abstract

Regenerative medicine and tissue engineering are reasonable techniques for repairing failed tissues and could be a suitable alternative to organ transplantation. One of the most widely used methods for preparing bioscaffolds is the decellularization procedure. Although cell debris and DNA are removed from the decellularized tissues, important compositions of the extracellular matrix including proteins, proteoglycans, and glycoproteins are nearly preserved. Moreover, the obtained scaffolds have a 3-dimensional (3D) structure, appropriate naïve mechanical properties, and good biocompatibility. After transplantation, different types of host cells migrate to the decellularized tissues. Histological and immunohistochemical assessment of the different bioscaffolds after implantation reveals the migration of parenchymal cells, angiogenesis, as well as the invasion of inflammatory and giant foreign cells. In this review, the events after transplantation including angiogenesis, scaffold degradation, and the presence of immune and tissue-specific progenitor cells in the decellularized scaffolds in various hosts, are discussed.

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Source
http://dx.doi.org/10.1016/j.trim.2022.101640DOI Listing

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