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GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice

Skeletal muscle insulin resistance is a main defect in type 2 diabetes (T2D), which is associated with impaired function and content of glucose transporter type 4 (GLUT4). GLUT4 overexpression in skeletal muscle tissue can improve glucose homeostasis. Therefore, we created an engineered muscle const...

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Autores principales: Beckerman, Margarita, Harel, Chava, Michael, Inbal, Klip, Amira, Bilan, Philip J., Gallagher, Emily J., LeRoith, Derek, Lewis, Eli C., Karnieli, Eddy, Levenberg, Shulamit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514095/
https://www.ncbi.nlm.nih.gov/pubmed/34644106
http://dx.doi.org/10.1126/sciadv.abg3947
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author Beckerman, Margarita
Harel, Chava
Michael, Inbal
Klip, Amira
Bilan, Philip J.
Gallagher, Emily J.
LeRoith, Derek
Lewis, Eli C.
Karnieli, Eddy
Levenberg, Shulamit
author_facet Beckerman, Margarita
Harel, Chava
Michael, Inbal
Klip, Amira
Bilan, Philip J.
Gallagher, Emily J.
LeRoith, Derek
Lewis, Eli C.
Karnieli, Eddy
Levenberg, Shulamit
author_sort Beckerman, Margarita
collection PubMed
description Skeletal muscle insulin resistance is a main defect in type 2 diabetes (T2D), which is associated with impaired function and content of glucose transporter type 4 (GLUT4). GLUT4 overexpression in skeletal muscle tissue can improve glucose homeostasis. Therefore, we created an engineered muscle construct (EMC) composed of GLUT4-overexpressing (OEG4) cells. The ability of the engineered implants to reduce fasting glucose levels was tested in diet-induced obesity mice. Decrease and stabilization of basal glucose levels were apparent up to 4 months after implantation. Analysis of the retrieved constructs showed elevated expression of myokines and proteins related to metabolic processes. In addition, we validated the efficiency of OEG4-EMCs in insulin-resistant mice. Following high glucose load administration, mice showed improved glucose tolerance. Our data indicate that OEG4-EMC implant is an efficient mode for restoring insulin sensitivity and improving glucose homeostasis in diabetic mice. Such procedure is a potential innovative modality for T2D therapy.
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spelling pubmed-85140952021-10-22 GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice Beckerman, Margarita Harel, Chava Michael, Inbal Klip, Amira Bilan, Philip J. Gallagher, Emily J. LeRoith, Derek Lewis, Eli C. Karnieli, Eddy Levenberg, Shulamit Sci Adv Biomedicine and Life Sciences Skeletal muscle insulin resistance is a main defect in type 2 diabetes (T2D), which is associated with impaired function and content of glucose transporter type 4 (GLUT4). GLUT4 overexpression in skeletal muscle tissue can improve glucose homeostasis. Therefore, we created an engineered muscle construct (EMC) composed of GLUT4-overexpressing (OEG4) cells. The ability of the engineered implants to reduce fasting glucose levels was tested in diet-induced obesity mice. Decrease and stabilization of basal glucose levels were apparent up to 4 months after implantation. Analysis of the retrieved constructs showed elevated expression of myokines and proteins related to metabolic processes. In addition, we validated the efficiency of OEG4-EMCs in insulin-resistant mice. Following high glucose load administration, mice showed improved glucose tolerance. Our data indicate that OEG4-EMC implant is an efficient mode for restoring insulin sensitivity and improving glucose homeostasis in diabetic mice. Such procedure is a potential innovative modality for T2D therapy. American Association for the Advancement of Science 2021-10-13 /pmc/articles/PMC8514095/ /pubmed/34644106 http://dx.doi.org/10.1126/sciadv.abg3947 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Beckerman, Margarita
Harel, Chava
Michael, Inbal
Klip, Amira
Bilan, Philip J.
Gallagher, Emily J.
LeRoith, Derek
Lewis, Eli C.
Karnieli, Eddy
Levenberg, Shulamit
GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title_full GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title_fullStr GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title_full_unstemmed GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title_short GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
title_sort glut4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514095/
https://www.ncbi.nlm.nih.gov/pubmed/34644106
http://dx.doi.org/10.1126/sciadv.abg3947
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