Ion-Pair-Enhanced Double-Click Driven Cell Adhesion and Altered Expression of Related Genes.
Kohei KitagawaNao OkumaMoeka YoshinagaHitoshi TakemaeFumiya SatoShoma SatoSeiichiro NakabayashiHiroshi Y YoshikawaMasami SuganumaNathan W LuedtkeTakahisa MatsuzakiMasayuki TeraPublished in: Bioconjugate chemistry (2023)
Bio-orthogonal ligations that crosslink living cells with a substrate or other cells require high stability and rapid kinetics to maintain the nature of target cells. In this study, we report water-soluble cyclooctadiyne (WS-CODY) derivatives that undergo an ion-pair enhanced double-click reaction. The cationic side chain of WS-CODY accelerated the kinetics on the azide-modified cell surface due to proximity effect. Cationic WS-CODY was able to crosslink azide-modified, poorly adherent human lung cancer PC-9 cells not only to azide-grafted glass substrates but also to other cells within 5-30 min. We discovered that cell-substrate crosslinking induced the ITGA5 gene expression, whereas cell-cell crosslinking induced the CTNNA1 gene, according to the adhesion partner. Ion-pair-enhanced WS-CODY can be applied to a wide range of cells with established azide modifications and is expected to provide a powerful tool to regulate cell-substrate and cell-cell interactions.
Keyphrases
- single cell
- induced apoptosis
- gene expression
- cell therapy
- cell cycle arrest
- living cells
- cell adhesion
- endothelial cells
- signaling pathway
- dna methylation
- cell death
- staphylococcus aureus
- genome wide
- stem cells
- transcription factor
- escherichia coli
- single molecule
- mesenchymal stem cells
- poor prognosis
- cell proliferation
- pseudomonas aeruginosa
- cell surface
- cystic fibrosis
- stress induced
- copy number
- drug induced
- induced pluripotent stem cells