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Thermofluidic heat exchangers for actuation of transcription in artificial tissues.
Corbett, Daniel C; Fabyan, Wesley B; Grigoryan, Bagrat; O'Connor, Colleen E; Johansson, Fredrik; Batalov, Ivan; Regier, Mary C; DeForest, Cole A; Miller, Jordan S; Stevens, Kelly R.
Afiliação
  • Corbett DC; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Fabyan WB; Institute for Stem Cell and Regenerative Medicine, Seattle, WA 98195, USA.
  • Grigoryan B; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • O'Connor CE; Institute for Stem Cell and Regenerative Medicine, Seattle, WA 98195, USA.
  • Johansson F; Department of Bioengineering, Rice University, Houston, TX 77005, USA.
  • Batalov I; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Regier MC; Institute for Stem Cell and Regenerative Medicine, Seattle, WA 98195, USA.
  • DeForest CA; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Miller JS; Institute for Stem Cell and Regenerative Medicine, Seattle, WA 98195, USA.
  • Stevens KR; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Sci Adv ; 6(40)2020 09.
Article em En | MEDLINE | ID: mdl-32998880
ABSTRACT
Spatial patterns of gene expression in living organisms orchestrate cell decisions in development, homeostasis, and disease. However, most methods for reconstructing gene patterning in 3D cell culture and artificial tissues are restricted by patterning depth and scale. We introduce a depth- and scale-flexible method to direct volumetric gene expression patterning in 3D artificial tissues, which we call "heat exchangers for actuation of transcription" (HEAT). This approach leverages fluid-based heat transfer from printed networks in the tissues to activate heat-inducible transgenes expressed by embedded cells. We show that gene expression patterning can be tuned both spatially and dynamically by varying channel network architecture, fluid temperature, fluid flow direction, and stimulation timing in a user-defined manner and maintained in vivo. We apply this approach to activate the 3D positional expression of Wnt ligands and Wnt/ß-catenin pathway regulators, which are major regulators of development, homeostasis, regeneration, and cancer throughout the animal kingdom.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Via de Sinalização Wnt / Temperatura Alta Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Via de Sinalização Wnt / Temperatura Alta Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article