Bioluminescent-based imaging and quantification of glucose uptake in vivo
Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold...
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Published in | Nature methods Vol. 16; no. 6; pp. 526 - 532 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.06.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1548-7091 1548-7105 1548-7105 |
DOI | 10.1038/s41592-019-0421-z |
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Abstract | Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used
18
F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development.
A bioluminescent glucose-uptake probe enables accurate, real-time, non-invasive longitudinal imaging of
d
-glucose absorption both in vitro and in vivo. |
---|---|
AbstractList | Glucose is a major source of energy for most living organisms and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited due to the lack of robust tools. To date, positron emission tomography (PET) imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in
in vivo
settings. Here we report the development of a novel bioluminescent glucose uptake probe (BiGluc) for real-time, non-invasive longitudinal imaging of glucose absorption both
in vitro
and
in vivo
. In addition, we demonstrate that the sensitivity of our method is comparable with commonly used
18
F-FDG-PET tracers and validate BiGluc as a tool for the identification of novel glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the field of metabolism and drug development. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used 18F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development.A bioluminescent glucose-uptake probe enables accurate, real-time, non-invasive longitudinal imaging of d-glucose absorption both in vitro and in vivo. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used .sup.18F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development. A bioluminescent glucose-uptake probe enables accurate, real-time, non-invasive longitudinal imaging of d-glucose absorption both in vitro and in vivo. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used 18F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development.Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used 18F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used .sup.18F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development. Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of disease-associated glucose flux is limited owing to the lack of robust tools. To date, positron-emission tomography imaging remains the gold standard for measuring glucose uptake, and no optical tools exist for non-invasive longitudinal imaging of this important metabolite in in vivo settings. Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-invasive longitudinal imaging of glucose absorption both in vitro and in vivo. In addition, we demonstrate that the sensitivity of our method is comparable with that of commonly used 18 F-FDG-positron-emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the identification of new glucose transport inhibitors. The new imaging reagent enables a wide range of applications in the fields of metabolism and drug development. A bioluminescent glucose-uptake probe enables accurate, real-time, non-invasive longitudinal imaging of d -glucose absorption both in vitro and in vivo. |
Audience | Academic |
Author | Jones, Anthony Bonhoure, Nicolas Mikhaylov, Georgy Sinisi, Riccardo Goun, Elena Abdelhady, Gihad Khodakivskyi, Pavlo Yevtodiyenko, Aleksey Shackelford, David Muhunthan, Vishaka Bazhin, Arkadiy Maric, Tamara |
AuthorAffiliation | 3 Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, USA 1 Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland 2 Nestlé Institute of Health Sciences SA, EPFL Innovation Park, Bâtiments G/H, Lausanne, Switzerland |
AuthorAffiliation_xml | – name: 2 Nestlé Institute of Health Sciences SA, EPFL Innovation Park, Bâtiments G/H, Lausanne, Switzerland – name: 3 Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, USA – name: 1 Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland |
Author_xml | – sequence: 1 givenname: Tamara orcidid: 0000-0002-2512-4371 surname: Maric fullname: Maric, Tamara organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) – sequence: 2 givenname: Georgy surname: Mikhaylov fullname: Mikhaylov, Georgy organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL), Jožef Stefan Institute – sequence: 3 givenname: Pavlo surname: Khodakivskyi fullname: Khodakivskyi, Pavlo organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) – sequence: 4 givenname: Arkadiy orcidid: 0000-0002-7929-9302 surname: Bazhin fullname: Bazhin, Arkadiy organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) – sequence: 5 givenname: Riccardo surname: Sinisi fullname: Sinisi, Riccardo organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) – sequence: 6 givenname: Nicolas surname: Bonhoure fullname: Bonhoure, Nicolas organization: Nestlé Institute of Health Sciences SA, EPFL Innovation Park, Bâtiments G/H – sequence: 7 givenname: Aleksey surname: Yevtodiyenko fullname: Yevtodiyenko, Aleksey organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) – sequence: 8 givenname: Anthony surname: Jones fullname: Jones, Anthony organization: Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California – sequence: 9 givenname: Vishaka surname: Muhunthan fullname: Muhunthan, Vishaka organization: Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California – sequence: 10 givenname: Gihad surname: Abdelhady fullname: Abdelhady, Gihad organization: Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California – sequence: 11 givenname: David surname: Shackelford fullname: Shackelford, David organization: Department of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California – sequence: 12 givenname: Elena orcidid: 0000-0002-4214-0656 surname: Goun fullname: Goun, Elena email: elena.goun@epfl.ch organization: Institute of Chemical Sciences and Engineering (ISIC), Swiss Federal Institute of Technology (EPFL) |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31086341$$D View this record in MEDLINE/PubMed |
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Snippet | Glucose is a major source of energy for most living organisms, and its aberrant uptake is linked to many pathological conditions. However, our understanding of... Glucose is a major source of energy for most living organisms and its aberrant uptake is linked to many pathological conditions. However, our understanding of... |
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Title | Bioluminescent-based imaging and quantification of glucose uptake in vivo |
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