| Literature DB >> 30058274 |
Heinz P Janke1, Nihan Güvener2,3, Weiqiang Dou4,5, Dorien M Tiemessen1, Anglita YantiSetiasti1,6, Jozef G O Cremers2,3, Paul J A Borm3, Wout F J Feitz1,7, Arend Heerschap4, Fabian Kiessling2, Egbert Oosterwijk1.
Abstract
In vivo monitoring of tissue-engineered constructs is important to assess their integrity, remodeling, and degradation. However, this is challenging when the contrast with neighboring tissues is low, necessitating labeling with contrast agents (CAs), but current CAs have limitations (i.e., toxicity, negative contrast, label instability, and/or inappropriate size). Therefore, a naturally derived hemin-L-lysine (HL) complex is used as a potential CA to label collagen-based templates for magnetic resonance imaging (MRI). Labeling does not change the basic characteristics of the collagen templates. When hybrid templates composed of collagen type I reinforced with degradable polymers are subcutaneously implanted in mice, longitudinal visualization by MRI is possible with good contrast and in correlation with template remodeling. In contrast, unlabeled collagen templates are hardly detectable and the fate of these templates cannot be monitored by MRI. Interestingly, tissue remodeling and vascularization are enhanced within HL-labeled templates. Thus, HL labeling is presented as a promising universal imaging marker to label tissue-engineered implants for MRI, which additionally seems to accelerate tissue regeneration.Entities:
Keywords: collagen type I; contrast agents; hemin-L-lysine; magnetic resonance imaging; tissue engineering
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Year: 2018 PMID: 30058274 DOI: 10.1002/adhm.201800605
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933