Investigation of Collagen Network Microstructure and Vascular Sprouting On-Chip Using Non-enzymatic Glycation

Non-enzymatic glycation of collagen, a post-translational modificationprocess, creates extra crosslinks between collagen molecules. The accumulation of advanced glycation end-product crosslinks is one of the main phenomena observed in connective tissue of subjects with diabetes and aging, and many s...

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Published inBiochip journal Vol. 19; no. 2; pp. 301 - 312
Main Authors Choi, BongHwan, Ahn, Jinchul, Choi, Dong-Hee, Oh, Dongwoo, Shin, Seung-cheol, Yang, Ji Hun, Jang, Hwanseok, Chung, Seok
Format Journal Article
LanguageEnglish
Published Seoul The Korean BioChip Society (KBCS) 01.06.2025
Springer Nature B.V
한국바이오칩학회
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Abstract Non-enzymatic glycation of collagen, a post-translational modificationprocess, creates extra crosslinks between collagen molecules. The accumulation of advanced glycation end-product crosslinks is one of the main phenomena observed in connective tissue of subjects with diabetes and aging, and many studies showed the alteration of microstructure of collagen network by these glycation-mediated crosslinks. However, the effects of the glycation-induced collagen network changes on adjacent cells, particularly in growth and tissue formation, remain largely unexplored. Here, we present a microfluidic model to investigate vascular sprouting in glycated collagen networks under well-controlled conditions. Using scanning electron microscopy, fluorescence labeling microscopy (NHS-ester), and label-free microscopy (second harmonic generation microscopy), we characterized the microstructure of collagen networks across different ribose concentrations. Three-dimensional vascular sprouting analysis revealed that the higher ribose concentrations resulted in longer and thicker vascular sprouts. Finally, we investigated the alteration of gene expressions in endothelial cells by glycated collagen hydrogels with VEGF gradients. This study enhances our understanding of how glycation-induced changes in collagen affect vascular growth, providing insights into tissue formation in pathological conditions.
AbstractList Non-enzymatic glycation of collagen, a post-translational modificationprocess, creates extra crosslinks between collagen molecules. The accumulation of advanced glycation end-product crosslinks is one of the main phenomena observed in connective tissue of subjects with diabetes and aging, and many studies showed the alteration of microstructure of collagen network by these glycation-mediated crosslinks. However, the effects of the glycation-induced collagen network changes on adjacent cells, particularly in growth and tissue formation, remain largely unexplored. Here, we present a microfluidic model to investigate vascular sprouting in glycated collagen networks under well-controlled conditions. Using scanning electron microscopy, fluorescence labeling microscopy (NHS-ester), and label-free microscopy (second harmonic generation microscopy), we characterized the microstructure of collagen networks across different ribose concentrations. Three-dimensional vascular sprouting analysis revealed that the higher ribose concentrations resulted in longer and thicker vascular sprouts. Finally, we investigated the alteration of gene expressions in endothelial cells by glycated collagen hydrogels with VEGF gradients. This study enhances our understanding of how glycation-induced changes in collagen affect vascular growth, providing insights into tissue formation in pathological conditions.
Non-enzymatic glycation of collagen, a post-translational modificationprocess, creates extra crosslinks between collagen molecules. The accumulation of advanced glycation end-product crosslinks is one of the main phenomena observed in con-nective tissue of subjects with diabetes and aging, and many studies showed the alteration of microstructure of collagen network by these glycation-mediated crosslinks. However, the effects of the glycation-induced collagen network changes on adjacent cells, particularly in growth and tissue formation, remain largely unexplored. Here, we present a microfluidic model to investigate vascular sprouting in glycated collagen networks under well-controlled conditions. Using scanning electron microscopy, fluorescence labeling microscopy (NHS-ester), and label-free microscopy (second harmonic generation micros-copy), we characterized the microstructure of collagen networks across different ribose concentrations. Three-dimensional vascular sprouting analysis revealed that the higher ribose concentrations resulted in longer and thicker vascular sprouts. Finally, we investigated the alteration of gene expressions in endothelial cells by glycated collagen hydrogels with VEGF gradients. This study enhances our understanding of how glycation-induced changes in collagen affect vascular growth, providing insights into tissue formation in pathological conditions. KCI Citation Count: 0
Author Ahn, Jinchul
Chung, Seok
Jang, Hwanseok
Choi, Dong-Hee
Oh, Dongwoo
Choi, BongHwan
Shin, Seung-cheol
Yang, Ji Hun
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Keywords Microfluidic chip
Non-enzymatic glycation
Angiogenesis
Collagen network
Vascular sprouting
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Snippet Non-enzymatic glycation of collagen, a post-translational modificationprocess, creates extra crosslinks between collagen molecules. The accumulation of...
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SubjectTerms Angiogenesis
Biomedical Engineering and Bioengineering
Biotechnology
Chemistry
Chemistry and Materials Science
Collagen
Connective tissues
Controlled conditions
Cross-linking
Crosslinking
Diabetes mellitus
Endothelial cells
Frequency distribution
Glycosylation
Hydrogels
Labels
Microfluidics
Microscopy
Microstructure
Original Article
Pore size
Post-translation
Ribose
Scanning electron microscopy
Second harmonic generation
Three dimensional analysis
Vascular endothelial growth factor
생물공학
Title Investigation of Collagen Network Microstructure and Vascular Sprouting On-Chip Using Non-enzymatic Glycation
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