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Nonimmune cells equipped with T-cell-receptor-like signaling for cancer cell ablation.
Kojima, Ryosuke; Scheller, Leo; Fussenegger, Martin.
Afiliação
  • Kojima R; ETH Zurich, Department of Biosystems Science and Engineering, Basel, Switzerland.
  • Scheller L; ETH Zurich, Department of Biosystems Science and Engineering, Basel, Switzerland.
  • Fussenegger M; ETH Zurich, Department of Biosystems Science and Engineering, Basel, Switzerland.
Nat Chem Biol ; 14(1): 42-49, 2018 Jan.
Article em En | MEDLINE | ID: mdl-29131143
ABSTRACT
The ability to engineer custom cell-contact-sensing output devices into human nonimmune cells would be useful for extending the applicability of cell-based cancer therapies and for avoiding risks associated with engineered immune cells. Here we have developed a new class of synthetic T-cell receptor-like signal-transduction device that functions efficiently in human nonimmune cells and triggers release of output molecules specifically upon sensing contact with a target cell. This device employs an interleukin signaling cascade, whose OFF/ON switching is controlled by biophysical segregation of a transmembrane signal-inhibitory protein from the sensor cell-target cell interface. We further show that designer nonimmune cells equipped with this device driving expression of a membrane-penetrator/prodrug-activating enzyme construct could specifically kill target cells in the presence of the prodrug, indicating its potential usefulness for target-cell-specific, cell-based enzyme-prodrug cancer therapy. Our study also contributes to the advancement of synthetic biology by extending available design principles to transmit extracellular information to cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Transdução de Sinais / Células-Tronco Mesenquimais / Engenharia Celular / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T / Transdução de Sinais / Células-Tronco Mesenquimais / Engenharia Celular / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article