4.7 Article

Air-loaded Gas Vesicle Nanoparticles Promote Cell Growth in Three-dimensional Bioprinted Tissue Constructs

期刊

INTERNATIONAL JOURNAL OF BIOPRINTING
卷 8, 期 3, 页码 69-81

出版社

WHIOCE PUBL PTE LTD
DOI: 10.18063/ijb.v8i3.489

关键词

Three-dimensional bioprinting; Gas vesicles; Halobacterium; Haloferax; Tissue engineering

资金

  1. King Abdullah University of Science and Technology
  2. University of Jeddah

向作者/读者索取更多资源

Three-dimensional bioprinting is a promising method for tissue and organ engineering. However, the development of bioink materials and the diffusion barrier in scaffold materials limit its widespread use. In this study, genetically encoded gas vesicles derived from haloarchaea were used to promote oxygen diffusion in printed constructs. The results showed that cells printed with gas vesicles had increased activity and proliferation, suggesting that gas vesicles can overcome the diffusion barrier and increase oxygen availability in bioprinted constructs. The biodegradable nature of gas vesicle proteins makes them a potential oxygen-promoting material in biological samples.
Three-dimensional (3D) bioprinting has emerged as a promising method for the engineering of tissues and organs. Still, it faces challenges in its widespread use due to issues with the development of bioink materials and the nutrient diffusion barrier inherent to these scaffold materials. Herein, we introduce a method to promote oxygen diffusion throughout the printed constructs using genetically encoded gas vesicles derived from haloarchaea. These hollow nanostructures are composed of a protein shell that allows gases to permeate freely while excluding the water flow. After printing cells with gas vesicles of various concentrations, the cells were observed to have increased activity and proliferation. These results suggest that air-filled gas vesicles can help overcome the diffusion barrier throughout the 3D bioprinted constructs by increasing oxygen availability to cells within the center of the construct. The biodegradable nature of the gas vesicle proteins combined with our promising results encourage their potential use as oxygen-promoting materials in biological samples.

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