Intrinsic Vascularization of Recombinant eADF4(C16) Spider Silk Matrices in the Arteriovenous Loop Model

2019 ◽  
Vol 25 (21-22) ◽  
pp. 1504-1513 ◽  
Author(s):  
Dominik Steiner ◽  
Gregor Lang ◽  
Laura Fischer ◽  
Sophie Winkler ◽  
Tobias Fey ◽  
...  
2021 ◽  
Author(s):  
Dominik Steiner ◽  
Sophie Winkler ◽  
Stefanie Heltmann-Meyer ◽  
Vanessa Trossmann ◽  
Tobias Fey ◽  
...  

Author(s):  
Jan W. Robering ◽  
Majida Al-Abboodi ◽  
Adriana Titzmann ◽  
Inge Horn ◽  
Justus P. Beier ◽  
...  

2011 ◽  
Vol 46 (3) ◽  
pp. 148-155 ◽  
Author(s):  
J.P. Beier ◽  
A. Hess ◽  
J. Loew ◽  
J. Heinrich ◽  
A.M. Boos ◽  
...  

2012 ◽  
Vol 7 (8) ◽  
pp. 654-664 ◽  
Author(s):  
Anja M. Boos ◽  
Johanna S. Loew ◽  
Annika Weigand ◽  
Gloria Deschler ◽  
Dorothee Klumpp ◽  
...  

2010 ◽  
Vol 27 (01) ◽  
pp. 011-018 ◽  
Author(s):  
Elias Polykandriotis ◽  
Dimitris Drakotos ◽  
Andreas Arkudas ◽  
Galyna Pryymachuk ◽  
Subha Rath ◽  
...  

2013 ◽  
Vol 19 (6) ◽  
pp. 479-486 ◽  
Author(s):  
Andreas Arkudas ◽  
Amelie Balzer ◽  
Gregor Buehrer ◽  
Isabel Arnold ◽  
Alexander Hoppe ◽  
...  

2016 ◽  
Vol 2 (1) ◽  
Author(s):  
Gregor Bührer ◽  
Ulrike Rottensteiner ◽  
Alexander Hoppe ◽  
Rainer Detsch ◽  
Diana Dafinova ◽  
...  

Abstracteffects of 3D scaffolds made from 45S5 bioactive glass (BG) doped with 1 wt. % copper ions in the arteriovenous loop model of the rat.Materials and Methods: An arteriovenous loop was built in the groin of 10 rats and inserted in 1% copper doped 45S5 BG scaffolds and fibrin. The scaffold and the AV loop were inserted in Teflon isolation chambers and explanted 3 weeks after implantation. Afterwards the scaffolds were analyzed by Micro-CT and histology regarding vascularization. Results were compared to plain 45S5 BG-based scaffolds from a previous study.Results: Micro-CT and histological evaluation showed consistent vascularization of the constructs. A tendency towards an increased vascularization in the copper doped BG group compared to plain BG constructs could be observed. However, therewas no significant difference in statistical analysis between both groups.Conclusions: This study shows results that support an increased angiogenetic effect of 1% copper doped 45S5 BG compared to regular 45S5 BG scaffolds in the rat arteriovenous loop model although these tendencies are not backed by statistical evidence. Maybe higher copper doses could lead to a statistically significant angiogenetic effect.


2016 ◽  
Vol 79 (10) ◽  
pp. 899-907 ◽  
Author(s):  
Hannes Seuss ◽  
Andreas Arkudas ◽  
Matthias Hammon ◽  
Oliver Bleiziffer ◽  
Michael Uder ◽  
...  

2014 ◽  
Vol 56 ◽  
pp. 207-219 ◽  
Author(s):  
Chi L.L. Pham ◽  
Ann H. Kwan ◽  
Margaret Sunde

Amyloids are insoluble fibrillar protein deposits with an underlying cross-β structure initially discovered in the context of human diseases. However, it is now clear that the same fibrillar structure is used by many organisms, from bacteria to humans, in order to achieve a diverse range of biological functions. These functions include structure and protection (e.g. curli and chorion proteins, and insect and spider silk proteins), aiding interface transitions and cell–cell recognition (e.g. chaplins, rodlins and hydrophobins), protein control and storage (e.g. Microcin E492, modulins and PMEL), and epigenetic inheritance and memory [e.g. Sup35, Ure2p, HET-s and CPEB (cytoplasmic polyadenylation element-binding protein)]. As more examples of functional amyloid come to light, the list of roles associated with functional amyloids has continued to expand. More recently, amyloids have also been implicated in signal transduction [e.g. RIP1/RIP3 (receptor-interacting protein)] and perhaps in host defence [e.g. aDrs (anionic dermaseptin) peptide]. The present chapter discusses in detail functional amyloids that are used in Nature by micro-organisms, non-mammalian animals and mammals, including the biological roles that they play, their molecular composition and how they assemble, as well as the coping strategies that organisms have evolved to avoid the potential toxicity of functional amyloid.


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