Bacteriophage-based biomaterials for tissue regeneration.

Adv Drug Deliv Rev

Department of Chemistry & Biochemistry, Stephenson Life Science Research Center, Institute for Biomedical Engineering, Science and Technology, University of Oklahoma, 101 Stephenson Parkway, Norman, OK 73019, United States; School of Materials Science and Engineering, Zhejiang University, Hangzhou, Zhejiang 310027, China. Electronic address:

Published: May 2019

AI Article Synopsis

  • Bacteriophages, or phages, are safe viruses that specifically target bacteria and are made up of proteins and nucleic acids.
  • Filamentous phages are particularly notable in tissue regeneration research due to their nanofiber-like structure, which allows for error-free production and self-assembly into functional scaffolds.
  • These phages can guide stem cell differentiation for various tissue regeneration applications, such as bone, nerves, and skin, and the review will cover recent advancements and future prospects in this area.

Article Abstract

Bacteriophage, also called phage, is a human-safe bacteria-specific virus. It is a monodisperse biological nanostructure made of proteins (forming the outside surface) and nucleic acids (encased in the protein capsid). Among different types of phages, filamentous phages have received great attention in tissue regeneration research due to their unique nanofiber-like morphology. They can be produced in an error-free format, self-assemble into ordered scaffolds, display multiple signaling peptides site-specifically, and serve as a platform for identifying novel signaling or homing peptides. They can direct stem cell differentiation into specific cell types when they are organized into proper patterns or display suitable peptides. These unusual features have allowed scientists to employ them to regenerate a variety of tissues, including bone, nerves, cartilage, skin, and heart. This review will summarize the progress in the field of phage-based tissue regeneration and the future directions in this field.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522342PMC
http://dx.doi.org/10.1016/j.addr.2018.11.004DOI Listing

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