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  3. In Vivo Biocompatibility of Synechococcus sp. PCC 7002-Integrated Scaffolds for Skin Regeneration.
 

In Vivo Biocompatibility of Synechococcus sp. PCC 7002-Integrated Scaffolds for Skin Regeneration.

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BORIS DOI
10.48620/77192
Date of Publication
October 3, 2024
Publication Type
Article
Division/Institute

Institute of Anatomy

Author
Fuchs, Benedikt
Mert, Sinan
Kuhlmann, Constanze
Birt, Alexandra
Hofmann, Daniel
Wiggenhauser, Paul Severin
Giunta, Riccardo E
Chavez, Myra N.
Institute of Anatomy
Nickelsen, Jörg
Schenck, Thilo Ludwig
Moellhoff, Nicholas
Subject(s)

600 - Technology::610...

Series
Journal of Functional Biomaterials
ISSN or ISBN (if monograph)
2079-4983
Publisher
MDPI
Language
English
Publisher DOI
10.3390/jfb15100295
PubMed ID
39452593
Uncontrolled Keywords

Synechococcus sp. PCC...

biocompatibility

biomaterials

cyanobacteria

scaffolds

tissue engineering

Description
Cyanobacteria, commonly known as blue-green algae, are prevalent in freshwater systems and have gained interest for their potential in medical applications, particularly in skin regeneration. Among these, Synechococcus sp. strain PCC 7002 stands out because of its rapid proliferation and capacity to be genetically modified to produce growth factors. This study investigates the safety of Synechococcus sp. PCC 7002 when used in scaffolds for skin regeneration, focusing on systemic inflammatory responses in a murine model. We evaluated the following three groups: scaffolds colonized with genetically engineered bacteria producing hyaluronic acid, scaffolds with wild-type bacteria, and control scaffolds without bacteria. After seven days, we assessed systemic inflammation by measuring changes in cytokine profiles and lymphatic organ sizes. The results showed no significant differences in spleen, thymus, and lymph node weights, indicating a lack of overt systemic toxicity. Blood cytokine analysis revealed elevated levels of IL-6 and IL-1β in scaffolds with bacteria, suggesting a systemic inflammatory response, while TNF-α levels remained unaffected. Proteome profiling identified distinct cytokine patterns associated with bacterial colonization, including elevated inflammatory proteins and products, indicative of acute inflammation. Conversely, control scaffolds exhibited protein profiles suggestive of a rejection response, characterized by increased levels of cytokines involved in T and B cell activation. Our findings suggest that Synechococcus sp. PCC 7002 does not appear to cause significant systemic toxicity, supporting its potential use in biomedical applications. Further research is necessary to explore the long-term effects and clinical implications of these responses.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/189450
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