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Programmed synthesis of 3D tissues
Reconstituting tissues from their cellular building blocks facilitates the modeling of morphogenesis, homeostasis, and disease in vitro. Here, we describe DNA Programmed Assembly of Cells (DPAC) to reconstitute the multicellular organization of tissues having programmed size, shape, composition, and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589502/ https://www.ncbi.nlm.nih.gov/pubmed/26322836 http://dx.doi.org/10.1038/nmeth.3553 |
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author | Todhunter, Michael E Jee, Noel Y Hughes, Alex J Coyle, Maxwell C Cerchiari, Alec Farlow, Justin Garbe, James C LaBarge, Mark A Desai, Tejal A Gartner, Zev J |
author_facet | Todhunter, Michael E Jee, Noel Y Hughes, Alex J Coyle, Maxwell C Cerchiari, Alec Farlow, Justin Garbe, James C LaBarge, Mark A Desai, Tejal A Gartner, Zev J |
author_sort | Todhunter, Michael E |
collection | PubMed |
description | Reconstituting tissues from their cellular building blocks facilitates the modeling of morphogenesis, homeostasis, and disease in vitro. Here, we describe DNA Programmed Assembly of Cells (DPAC) to reconstitute the multicellular organization of tissues having programmed size, shape, composition, and spatial heterogeneity. DPAC uses dissociated cells that are chemically functionalized with degradable oligonucleotide “velcro,” allowing rapid, specific, and reversible cell adhesion to other surfaces coated with complementary DNA sequences. DNA-patterned substrates function as removable and adhesive templates, and layer-by-layer DNA-programmed assembly builds arrays of tissues into the third dimension above the template. DNase releases completed arrays of microtissues from the template concomitant with full embedding in a variety of extracellular matrix (ECM) gels. DPAC positions subpopulations of cells with single-cell spatial resolution and generates cultures several centimeters long. We used DPAC to explore the impact of ECM composition, heterotypic cell-cell interactions, and patterns of signaling heterogeneity on collective cell behaviors. |
format | Online Article Text |
id | pubmed-4589502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-45895022016-04-01 Programmed synthesis of 3D tissues Todhunter, Michael E Jee, Noel Y Hughes, Alex J Coyle, Maxwell C Cerchiari, Alec Farlow, Justin Garbe, James C LaBarge, Mark A Desai, Tejal A Gartner, Zev J Nat Methods Article Reconstituting tissues from their cellular building blocks facilitates the modeling of morphogenesis, homeostasis, and disease in vitro. Here, we describe DNA Programmed Assembly of Cells (DPAC) to reconstitute the multicellular organization of tissues having programmed size, shape, composition, and spatial heterogeneity. DPAC uses dissociated cells that are chemically functionalized with degradable oligonucleotide “velcro,” allowing rapid, specific, and reversible cell adhesion to other surfaces coated with complementary DNA sequences. DNA-patterned substrates function as removable and adhesive templates, and layer-by-layer DNA-programmed assembly builds arrays of tissues into the third dimension above the template. DNase releases completed arrays of microtissues from the template concomitant with full embedding in a variety of extracellular matrix (ECM) gels. DPAC positions subpopulations of cells with single-cell spatial resolution and generates cultures several centimeters long. We used DPAC to explore the impact of ECM composition, heterotypic cell-cell interactions, and patterns of signaling heterogeneity on collective cell behaviors. 2015-08-31 2015-10 /pmc/articles/PMC4589502/ /pubmed/26322836 http://dx.doi.org/10.1038/nmeth.3553 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Todhunter, Michael E Jee, Noel Y Hughes, Alex J Coyle, Maxwell C Cerchiari, Alec Farlow, Justin Garbe, James C LaBarge, Mark A Desai, Tejal A Gartner, Zev J Programmed synthesis of 3D tissues |
title | Programmed synthesis of 3D tissues |
title_full | Programmed synthesis of 3D tissues |
title_fullStr | Programmed synthesis of 3D tissues |
title_full_unstemmed | Programmed synthesis of 3D tissues |
title_short | Programmed synthesis of 3D tissues |
title_sort | programmed synthesis of 3d tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589502/ https://www.ncbi.nlm.nih.gov/pubmed/26322836 http://dx.doi.org/10.1038/nmeth.3553 |
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