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Electron Microscopy for 3D Scaffolds-Cell Biointerface Characterization. | LitMetric

AI Article Synopsis

  • Cell fate is influenced by how cells interact with their microenvironment, making it essential to study these interactions for advancing tissue engineering.
  • Current tools for studying cell-material interactions work well in 2D cultures, but there's a need for better methods in 3D environments that mimic real living tissues.
  • This study introduces a new technique using scanning electron microscopy and focused ion beam to analyze cell interactions with 3D scaffolds, revealing important details about cell adhesion that could improve tissue-engineering strategies.

Article Abstract

Cell fate is largely determined by interactions that occur at the interface between cells and their surrounding microenvironment. For this reason, especially in the field of tissue-engineering, there is a growing interest in developing techniques that allow evaluating cell-material interaction at the nanoscale, particularly focusing on cell adhesion processes. While for 2D culturing systems a consolidated series of tools already satisfy this need, in 3D environments, more closely recapitulating complex in vivo structures, there is still a lack of procedures furthering the comprehension of cell-material interactions. Here, the use of scanning electron microscopy coupled with a focused ion beam (SEM/FIB) for the characterization of cell interactions with 3D scaffolds obtained by different fabrication techniques is reported for the first time. The results clearly show the capability of the developed approach to preserve and finely resolve scaffold-cell interfaces highlighting details such as plasma membrane arrangement, extracellular matrix architecture and composition, and cellular structures playing a role in cell adhesion to the surface. It is anticipated that the developed approach will be relevant for the design of efficient cell-instructive platforms in the study of cellular guidance strategies for tissue-engineering applications as well as for in vitro 3D models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340848PMC
http://dx.doi.org/10.1002/adbi.201800103DOI Listing

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