Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability
Transplantation of immuno-isolated islets is a promising strategy to restore insulin-secreting function in patients with Type 1 diabetes. However, the clinical translation of this treatment approach remains elusive due to the loss of islet viability resulting from hypoxia at the avascular transpl...
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sg-ntu-dr.10356-1618572023-06-21T08:38:59Z Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability Chen, Yang Nguyen, Dang Tri Kokil, Ganesh Rajendra Wong, Yun Xuan Dang, Tram Thuy School of Chemical and Biomedical Engineering School of Chemistry, Chemical Engineering and Biotechnology Engineering::Chemical engineering Islet-Like Microtissue Toroid Microtissue Geometry Encapsulation Diabetes Cellular Viability Transplantation of immuno-isolated islets is a promising strategy to restore insulin-secreting function in patients with Type 1 diabetes. However, the clinical translation of this treatment approach remains elusive due to the loss of islet viability resulting from hypoxia at the avascular transplantation site. To address this challenge, we designed non-spherical islet-like microtissues and investigated the effect of their geometries on cellular viability. Insulinsecreting microtissues with different shapes were fabricated by assembly of monodispersed rat insulinoma beta cells on micromolded nonadhesive hydrogels. Our study quantitatively demonstrated that toroid microtissues exhibited enhanced cellular viability and metabolic activity compared to rod and spheroid microtissues with the same volume. At a similar level of cellular viability, toroid geometry facilitated efficient packing of more cells into each microtissue than rod and spheroid geometries. In addition, toroid microtissues maintained the characteristic glucose-responsive insulin secretion of rat-derived beta cells. Furthermore, toroid microtissues preserved their geometry and structural integrity following their microencapsulation in immuno-isolatory alginate hydrogel. Our study suggests that adopting toroid geometry in designing therapeutic microtissues potentially reduces mass loss of cellular grafts and thereby may improve the performance of transplanted islets towards a clinically viable cure for Type 1 diabetes. Ministry of Education (MOE) Nanyang Technological University Submitted/Accepted version This work was supported by the Start-up Grant (M4081759.120) from Nanyang Technological University and the Singapore Ministry of Education Academic Research Fund Tier 1 (M4012023.120 RG51/18). 2022-09-22T04:36:30Z 2022-09-22T04:36:30Z 2019 Journal Article Chen, Y., Nguyen, D. T., Kokil, G. R., Wong, Y. X. & Dang, T. T. (2019). Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability. Acta Biomaterialia, 97, 260-271. https://dx.doi.org/10.1016/j.actbio.2019.08.018 1742-7061 https://hdl.handle.net/10356/161857 10.1016/j.actbio.2019.08.018 97 260 271 en M4081759.120 M4012023.120-RG51/18 Acta Biomaterialia © 2019 Acta Materialia Inc. All rights reserved. This paper was published by Elsevier Ltd in Acta Biomaterialia and is made available with permission of Acta Materialia Inc. application/pdf |
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Engineering::Chemical engineering Islet-Like Microtissue Toroid Microtissue Geometry Encapsulation Diabetes Cellular Viability |
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Engineering::Chemical engineering Islet-Like Microtissue Toroid Microtissue Geometry Encapsulation Diabetes Cellular Viability Chen, Yang Nguyen, Dang Tri Kokil, Ganesh Rajendra Wong, Yun Xuan Dang, Tram Thuy Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
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Transplantation of immuno-isolated islets is a promising strategy to restore insulin-secreting
function in patients with Type 1 diabetes. However, the clinical translation of this treatment
approach remains elusive due to the loss of islet viability resulting from hypoxia at the
avascular transplantation site. To address this challenge, we designed non-spherical islet-like
microtissues and investigated the effect of their geometries on cellular viability. Insulinsecreting microtissues with different shapes were fabricated by assembly of monodispersed
rat insulinoma beta cells on micromolded nonadhesive hydrogels. Our study quantitatively
demonstrated that toroid microtissues exhibited enhanced cellular viability and metabolic
activity compared to rod and spheroid microtissues with the same volume. At a similar level
of cellular viability, toroid geometry facilitated efficient packing of more cells into each
microtissue than rod and spheroid geometries. In addition, toroid microtissues maintained the
characteristic glucose-responsive insulin secretion of rat-derived beta cells. Furthermore,
toroid microtissues preserved their geometry and structural integrity following their
microencapsulation in immuno-isolatory alginate hydrogel. Our study suggests that adopting
toroid geometry in designing therapeutic microtissues potentially reduces mass loss of
cellular grafts and thereby may improve the performance of transplanted islets towards a
clinically viable cure for Type 1 diabetes. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Chen, Yang Nguyen, Dang Tri Kokil, Ganesh Rajendra Wong, Yun Xuan Dang, Tram Thuy |
format |
Article |
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Chen, Yang Nguyen, Dang Tri Kokil, Ganesh Rajendra Wong, Yun Xuan Dang, Tram Thuy |
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Chen, Yang |
title |
Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
title_short |
Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
title_full |
Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
title_fullStr |
Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
title_full_unstemmed |
Microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
title_sort |
microencapsulated islet-like microtissues with toroid geometry for enhanced cellular viability |
publishDate |
2022 |
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https://hdl.handle.net/10356/161857 |
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