4.8 Article

Bioorthogonal Click Chemistry-Based Synthetic Cell Glue

Journal

SMALL
Volume 11, Issue 48, Pages 6458-6466

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201502972

Keywords

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Funding

  1. US National Science Foundation [ECCS-1264356]
  2. Department of Defense [FA9550-11-1-0331]
  3. National Research Foundation of Korea [2012R1A2A2A06045773]
  4. National IT Industry Promotion Agency (IT Consilience Creative Program) [NIPA-2014-H0201-14-1001]
  5. Medical Discovery Postdoctoral Fellowship Award from MGH
  6. Ministry of Science, ICT & Future Planning, Republic of Korea [IBS-R015-D1-2015-A00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [2012R1A2A2A06045773] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. Directorate For Engineering [1264356] Funding Source: National Science Foundation
  9. Div Of Chem, Bioeng, Env, & Transp Sys [1264356] Funding Source: National Science Foundation

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Artificial methods of cell adhesion can be effective in building functional cell complexes in vitro, but methods for in vivo use are currently lacking. Here, a chemical cell glue based on bioorthogonal click chemistry with high stability and robustness is introduced. Tetrazine (Tz) and trans-cyclooctene (TCO) conjugated to the cell surface form covalent bonds between cells within 10 min in aqueous conditions. Glued, homogeneous, or heterogeneous cell pairs remain viable and stably attached in a microfluidic flow channel at a shear stress of 20 dyn cm(-2). Upon intravenous injection of assembled Jurkat T cells into live mice, fluorescence microscopy shows the trafficking of cell pairs in circulation and their infiltration into lung tissues. These results demonstrate the promising potential of chemically glued cell pairs for various applications ranging from delivering therapeutic cells to studying cell-cell interactions in vivo.

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