| Literature DB >> 24700601 |
Kari Gabrielse1, Amit Gangar, Nigam Kumar, Jae Chul Lee, Adrian Fegan, Jing Jing Shen, Qing Li, Daniel Vallera, Carston R Wagner.
Abstract
The ability to engineer and re-program the surfaces of cells would provide an enabling synthetic biological method for the design of cell- and tissue-based therapies. A new cell surface-engineering strategy is described that uses lipid-chemically self-assembled nanorings (lipid-CSANs) that can be used for the stable and reversible modification of any cell surface with a molecular reporter or targeting ligand. In the presence of a non-toxic FDA-approved drug, the nanorings were quickly disassembled and the cell-cell interactions reversed. Similar to T-cells genetically engineered to express chimeric antigen receptors (CARS), when activated peripheral blood mononuclear cells (PBMCs) were functionalized with the anti-EpCAM-lipid-CSANs, they were shown to selectively kill antigen-positive cancer cells. Taken together, these results demonstrate that lipid-CSANs have the potential to be a rapid, stable, and general method for the reversible engineering of cell surfaces and cell-cell interactions.Entities:
Keywords: cell-cell interactions; chimeric antigen receptors; nanoparticles; oligomerization; self-assembly
Mesh:
Year: 2014 PMID: 24700601 DOI: 10.1002/anie.201310645
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336