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Flexibility in Organ Research

Flexibility in Organ Research

Dagmar Brislinger (ORCID: 0000-0002-7319-5377)
  • Grant DOI 10.55776/PIR7
  • Funding program Partnership in Research
  • Status ended
  • Start February 1, 2017
  • End January 31, 2021
  • Funding amount € 252,050

Disciplines

Biology (30%); Medical-Theoretical Sciences, Pharmacy (70%)

Keywords

    3D cell culture, Perfused Cell Culture, Tissue Culture, Electrospinning

Abstract

In many cases promising results of cell culture experiments lead to a disappointing outcome when transferred to animal experiments or human clinical studies. The reason therefore is obvious. The gap between a two-dimensional cell culture experiment and a complete organism is difficult to bridge, thus results can hardly be related. Aim of this project is the establishment of a 3D Organ Lab Model which helps to investigate the biochemical processes and their pathologies in complete organs. Each organ, based on its function, is composed of specialized cells and has special needs, which are incorporated in this system. This model consists of a scaffold composed of fibers which enable different types of cells the arrangement of a three-dimensional structure similar to the human anatomy, histology, and physiology. These structures can be sectioned in defined regions, where cells are applied to conditions appropriate to their function and requirements (e.g. flow, different nutrition, or oxygen concentration). If needed the 3D Organ Lab Model can be additionally adapted if the cells get in direct cell-to-cell contact or communicate by biochemical factors. Results received from conventional two-dimensional cell culture could be proofed and extended within this system which then will be expanded in animal experiments and clinical studies on patients. Further, animal experiments and time (and money) consuming clinical studies could be reduced by eliminating results of two-dimensional experiments which could not be confirmed in the 3D Organ Lab Model. This project aims in the establishment of a human blood vessel model, a placenta model, and a model of the gut by the use of the 3D Organ Lab Model. Already available systems lack flexibility and do not respond to the needs of specialized cells in a three-dimensional network. This model has following advantages: 1) Different cell types are composed 2) in a three-dimensional network and could be cultivated 3) under diverse physical and chemical conditions 4) in defined regions, wherein 5) direct cell contact can be promoted or avoided. This model consists of an autoclavable und therefore re-usable cartridge and a flexible matrix for one-time use only. Therefore this project addresses companies dealing with manufacturing of cell culture lab ware, but additionally companies developing membranes, fibers, and polymers for medical needs.

Research institution(s)
  • Medizinische Universität Graz - 100%
International project participants
  • Marc Müller, Leibniz Universität Hannover - Germany

Research Output

  • 45 Citations
  • 3 Publications
Publications
  • 2018
    Title Histological processing of un-/cellularized thermosensitive electrospun scaffolds
    DOI 10.1007/s00418-018-1757-7
    Type Journal Article
    Author Fuchs J
    Journal Histochemistry and Cell Biology
    Pages 343-356
    Link Publication
  • 2021
    Title Quantification of increased MUC5AC expression in airway mucus of smoker using an automated image-based approach
    DOI 10.1002/jemt.23879
    Type Journal Article
    Author Groiss S
    Journal Microscopy Research and Technique
    Pages 5-18
  • 2020
    Title Electrospun PCL/PLA Scaffolds Are More Suitable Carriers of Placental Mesenchymal Stromal Cells Than Collagen/Elastin Scaffolds and Prevent Wound Contraction in a Mouse Model of Wound Healing
    DOI 10.3389/fbioe.2020.604123
    Type Journal Article
    Author Vonbrunn E
    Journal Frontiers in Bioengineering and Biotechnology
    Pages 604123
    Link Publication

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