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Droplet Microfluidic Technology for the Early and Label-Free Isolation of Highly-Glycolytic, Activated T-Cells.
Zielke, Claudia; Gutierrez Ramirez, Adriana J; Voss, Kelsey; Ryan, Maya S; Gholizadeh, Azam; Rathmell, Jeffrey C; Abbyad, Paul.
Afiliación
  • Zielke C; Department of Chemistry and Biochemistry, Santa Clara University, Santa Clara, CA 95053, USA.
  • Gutierrez Ramirez AJ; Department of Chemistry and Biochemistry, Santa Clara University, Santa Clara, CA 95053, USA.
  • Voss K; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Ryan MS; Department of Chemistry and Biochemistry, Santa Clara University, Santa Clara, CA 95053, USA.
  • Gholizadeh A; Department of Chemistry and Biochemistry, Santa Clara University, Santa Clara, CA 95053, USA.
  • Rathmell JC; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Abbyad P; Vanderbilt Center for Immunobiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Micromachines (Basel) ; 13(9)2022 Sep 01.
Article en En | MEDLINE | ID: mdl-36144067
ABSTRACT
A label-free, fixation-free and passive sorting method is presented to isolate activated T-cells shortly after activation and prior to the display of activation surface markers. It uses a recently developed sorting platform dubbed "Sorting by Interfacial Tension" (SIFT) that sorts droplets based on pH. After polyclonal (anti-CD3/CD28 bead) activation and a brief incubation on chip, droplets containing activated T-cells display a lower pH than those containing naive cells due to increased glycolysis. Under specific surfactant conditions, a change in pH can lead to a concurrent increase in droplet interfacial tension. The isolation of activated T-cells on chip is hence achieved as flattened droplets are displaced as they encounter a micro-fabricated trench oriented diagonally with respect to the direction of flow. This technique leads to an enrichment of activated primary CD4+ T-cells to over 95% from an initial mixed population of naive cells and cells activated for as little as 15 min. Moreover, since the pH change is correlated to successful activation, the technique allows the isolation of T-cells with the earliest activation and highest glycolysis, an important feature for the testing of T-cell activation modulators and to determine regulators and predictors of differentiation outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Micromachines (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Micromachines (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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