Integrin-assisted T‑cell activation on nanostructured hydrogels
| Autor: | Jennifer Diemer, Judith Guasch, Joachim P. Spatz, Christine Anna Muth, Hossein Riahinezhad |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Integrins Nanostructure Materials science T-Lymphocytes T cell Integrin Biocompatible Materials Bioengineering Nanotechnology 02 engineering and technology Polyethylene glycol Lymphocyte Activation Peptides Cyclic Polyethylene Glycols Cell therapy 03 medical and health sciences chemistry.chemical_compound PEG ratio Cell Adhesion medicine Humans General Materials Science Cells Cultured Cell Proliferation biology Mechanical Engineering Hydrogels General Chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics medicine.disease Fibronectins Nanostructures Leukemia Immobilized Proteins 030104 developmental biology medicine.anatomical_structure chemistry Self-healing hydrogels Biophysics biology.protein 0210 nano-technology Oligopeptides |
| Zdroj: | Nano Letters |
| Popis: | Adoptive cell therapy (ACT) has shown very promising results as treatment for cancer in a few clinical trials, such as the complete remissions of otherwise terminal leukemia patients. Nevertheless, the introduction of ACT into clinics requires overcoming not only medical but also technical challenges, such as the ex vivo expansion of large amounts of specific T-cells. Nanostructured surfaces represent a novel T-cell stimulation technique that enables us to fine-tune the density and orientation of activating molecules presented to the cells. In this work, we studied the influence of integrin-mediated cell-adhesion on T-cell activation, proliferation, and differentiation using nanostructured surfaces, which provide a well-defined system at the nanoscale compared with standard cultures. Specifically, we synthesized a polymeric polyethylene glycol (PEG) hydrogel cross-linked with two fibronectin-derived peptides, cyclic Arg-Gly-Asp (cRGD) and cyclic Leu-Asp-Val (cLDV), that are known to activate different integrins. Moreover, the hydrogels were decorated with a quasi-hexagonal array of gold nanoparticles (AuNPs) functionalized with the activating antibody CD3 to initiate T-cell activation. Both cLDV and cRGD hydrogels showed higher T-cell activation (CD69 expression and IL-2 secretion) than nonfunctionalized PEG hydrogels. However, only the cRGD hydrogels clearly supported proliferation giving a higher proportion of cells with memory (CD4+CD45RO+) than naı̈ve (CD4+CD45RA+) phenotypes when interparticle distances smaller than 150 nm were used. Thus, T-cell proliferation can be enhanced by the activation of integrins through the RGD sequence. |
| Databáze: | OpenAIRE |
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