Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells

Diabetes is caused by the loss or dysfunction of insulin-secreting β-cells in the pancreas. β-cells reduce their mass and lose insulin-producing ability in vitro, likely due to insufficient cell-cell and cell-extracellular matrix (ECM) interactions as β-cells lose their native microenvironment. Here...

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Main Authors: Lee, Samuel, Ma, Minglin, Kim, Soo Min, Guye, Patrick, Pancoast, James R., Weiss, Ron, Lee, Richard T., Anderson, Daniel Griffith, Hammond, Paula T, Li, W.
Other Authors: Harvard University--MIT Division of Health Sciences and Technology
Format: Article
Language:en_US
Published: Nature Publishing Group 2014
Online Access:http://hdl.handle.net/1721.1/85010
https://orcid.org/0000-0003-0396-2443
https://orcid.org/0000-0001-5629-4798
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author Lee, Samuel
Ma, Minglin
Kim, Soo Min
Guye, Patrick
Pancoast, James R.
Weiss, Ron
Lee, Richard T.
Anderson, Daniel Griffith
Hammond, Paula T
Li, W.
author2 Harvard University--MIT Division of Health Sciences and Technology
author_facet Harvard University--MIT Division of Health Sciences and Technology
Lee, Samuel
Ma, Minglin
Kim, Soo Min
Guye, Patrick
Pancoast, James R.
Weiss, Ron
Lee, Richard T.
Anderson, Daniel Griffith
Hammond, Paula T
Li, W.
author_sort Lee, Samuel
collection MIT
description Diabetes is caused by the loss or dysfunction of insulin-secreting β-cells in the pancreas. β-cells reduce their mass and lose insulin-producing ability in vitro, likely due to insufficient cell-cell and cell-extracellular matrix (ECM) interactions as β-cells lose their native microenvironment. Herein, we built an ex-vivo cell microenvironment by culturing primary β-cells in direct contact with ‘synthetic neighbors', cell-sized soft polymer microbeads that were modified with cell-cell signaling factors as well as components from pancreatic-tissue-specific ECMs. This biomimetic 3D microenvironment was able to promote native cell-cell and cell-ECM interactions. We obtained sustained maintenance of β-cell function in vitro enhanced cell viability from the few days usually observed in 2D culture to periods exceeding three weeks, with enhanced β-cell stability and insulin production. Our approach can be extended to create a general 3D culture platform for other cell types.
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spelling mit-1721.1/850102022-09-27T22:51:16Z Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells Lee, Samuel Ma, Minglin Kim, Soo Min Guye, Patrick Pancoast, James R. Weiss, Ron Lee, Richard T. Anderson, Daniel Griffith Hammond, Paula T Li, W. Harvard University--MIT Division of Health Sciences and Technology Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Chemical Engineering Koch Institute for Integrative Cancer Research at MIT Li, Wei Ma, Minglin Anderson, Daniel Griffith Hammond, Paula T. Guye, Patrick Weiss, Ron Diabetes is caused by the loss or dysfunction of insulin-secreting β-cells in the pancreas. β-cells reduce their mass and lose insulin-producing ability in vitro, likely due to insufficient cell-cell and cell-extracellular matrix (ECM) interactions as β-cells lose their native microenvironment. Herein, we built an ex-vivo cell microenvironment by culturing primary β-cells in direct contact with ‘synthetic neighbors', cell-sized soft polymer microbeads that were modified with cell-cell signaling factors as well as components from pancreatic-tissue-specific ECMs. This biomimetic 3D microenvironment was able to promote native cell-cell and cell-ECM interactions. We obtained sustained maintenance of β-cell function in vitro enhanced cell viability from the few days usually observed in 2D culture to periods exceeding three weeks, with enhanced β-cell stability and insulin production. Our approach can be extended to create a general 3D culture platform for other cell types. National Science Foundation (U.S.). Emergent Behaviors of Integrated Cellular Systems David H. Koch Institute for Integrative Cancer Research at MIT Massachusetts Institute of Technology. Institute for Soldier Nanotechnologies 2014-02-19T17:30:39Z 2014-02-19T17:30:39Z 2013-10 2013-08 Article http://purl.org/eprint/type/JournalArticle 2045-2322 http://hdl.handle.net/1721.1/85010 Li, Wei, Samuel Lee, Minglin Ma, Soo Min Kim, Patrick Guye, James R. Pancoast, Daniel G. Anderson, Ron Weiss, Richard T. Lee, and Paula T. Hammond. “Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells.” Scientific Reports 3 (October 4, 2013). https://orcid.org/0000-0003-0396-2443 https://orcid.org/0000-0001-5629-4798 en_US http://dx.doi.org/10.1038/srep02863 Scientific Reports http://creativecommons.org/licenses/by-nc-nd/3.0/ application/pdf Nature Publishing Group Nature Publishing Group
spellingShingle Lee, Samuel
Ma, Minglin
Kim, Soo Min
Guye, Patrick
Pancoast, James R.
Weiss, Ron
Lee, Richard T.
Anderson, Daniel Griffith
Hammond, Paula T
Li, W.
Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title_full Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title_fullStr Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title_full_unstemmed Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title_short Microbead-based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β-cells
title_sort microbead based biomimetic synthetic neighbors enhance survival and function of rat pancreatic β cells
url http://hdl.handle.net/1721.1/85010
https://orcid.org/0000-0003-0396-2443
https://orcid.org/0000-0001-5629-4798
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