image: The trans-omic network includes regulatory pathways that are specific to obese mice and those specific to healthy mice. Color coding highlights pathways that respond to glucose only in normal-weight mice (WT, blue), only obese mice (ob/ob, red), pathways in common (green), and pathways that react in opposite ways in obese and normal-weight mice (pink). view more
Credit: Toshiya Kokaji, CC-BY, first published in Science Signaling, DOI: 10.1126/scisignal.aaz1236
Healthy cells and cells with Type 2 diabetes use completely different pathways to manage blood sugar levels, according to results from a study in mice. Researchers used a trans-omic approach, combining data from genes (transcriptomics) and metabolites (metabolomics) to identify and connect the many separate processes involved in responding to glucose.
"Many regulatory pathways for diabetes are already well known. What we have done is map the total landscape of diabetes regulation," said Professor Shinya Kuroda, leader of the Systems Biology Lab at the University of Tokyo. Kuroda's team previously mapped the different cell signaling pathways activated in response to high or low concentrations of insulin.
"We expected only small differences between the healthy and diabetes regulatory network, but we found they were totally different," said Kuroda.
Obese mice lack most of the rapid response to glucose found in healthy metabolism, instead relying on much slower methods like changing gene expression.
Building a trans-omic network of glucose response
After eating a meal or sugary drink, insulin triggers cells to allow glucose molecules to move from the blood into cells, where glucose is broken down and converted into energy. In Type 2 diabetes, cells become insensitive to insulin, so glucose remains in the blood causing prolonged high blood sugar levels known as hyperglycemia.
Decades of diabetes research have revealed that many signaling pathways become active when glucose is inside the cell. Many of those paths involve enzymes and small molecules called metabolites, which are themselves products of metabolic pathways.
Kuroda's team studied healthy mice and a strain of mouse with a genetic mutation that causes the mice to overeat and develop diabetes in adulthood. All mice drank sugary water and then researchers waited between 20 minutes to four hours before taking blood samples and dissecting their liver. The liver is a major site of glucose metabolism in both mice and humans.
Researchers used a wide range of experiments to identify molecules that changed in response to glucose.
After collecting the data, researchers searched scientific databases for information about any glucose-responsive molecule they had identified in their measurements. Knowledge in the databases allowed researchers to connect these individual molecules to networks of intercellular signaling pathways.
Trans-omics allows researchers to turn a long list of discrete measurements into a wide web of knowledge about how cells reacted to glucose.
The analysis was complicated by the fact that scientific databases are highly specialized, with different databases dedicated to individual types of molecules. For example, a database about genes is not connected to a database about enzymes.
Project Research Associate Toshiya Kokaji, first author of the research publication, estimates that it took four years to complete the data analysis and construct the trans-omic network.
"Now that the pipeline is defined, we can complete the data analysis and trans-omic network construction in one to two years," said Kokaji.
Researchers built a five-layered trans-omic map with information about insulin signaling, transcription factors (types of proteins that regulate gene activity), enzymes, metabolic reactions and metabolites.
Mapping cells' different glucose responses
Color-coding the glucose-responsive molecules that were measured in healthy or obese mice revealed the vastly different signaling paths they use.
Healthy mice rapidly respond to glucose using enzymes and metabolites produced as byproducts of glucose metabolism, returning to normal blood sugar levels in about one hour.
Obese mice lack most of this rapid response, instead changing the expression of some genes over several hours and producing different molecules to cope with the glucose.
This slower and very different approach in obese mice fits the typical understanding of diabetes as the global impairment of metabolic control. Additionally, the approach used in obese mice requires cells to expend more energy compared to the specific and specialized paths activated in healthy cells.
Researchers hope that the data contained in the trans-omic network will allow the research community to find new cell signaling pathways to explore, both generally and for glucose-specific metabolism.
The research team plans to continue their trans-omic analysis of glucose response by adding additional layers of information to the network and studying glucose response in other cell types that consume large amounts of glucose, such as muscle cells.
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This research paper is a peer-reviewed experimental study using mice published in Science Signaling. Collaborators across Japan at RIKEN Center for Integrative Medical Sciences, Keio University, University of Tsukuba, Kanazawa University and Kyushu University also contributed to this research.
Research Article
Toshiya Kokaji, Atsushi Hatano, Yuki Ito, Katsuyuki Yugi, Miki Eto, Keigo Morita, Satoshi Ohno, Masashi Fujii, Ken-ichi Hironaka1, Riku Egami, Akira Terakawa, Takaho Tsuchiya, Haruka Ozaki, Hiroshi Inoue, Shinsuke Uda, Hiroyuki Kubota, Yutaka Suzuki, Kazutaka Ikeda, Makoto Arita, Masaki Matsumoto, Keiichi I. Nakayama, Akiyoshi Hirayama, Tomoyoshi Soga, and Shinya Kuroda. 1 Dec 2020. Trans-omic analysis reveals allosteric and gene regulation-axes for altered glucose-responsive liver metabolism associated with obesity. Science Signaling. DOI: 10.1126/scisignal.aaz1236
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Kuroda Lab: http://kurodalab.bs.s.u-tokyo.ac.jp/en/research_en/
Graduate School of Science: https://www.s.u-tokyo.ac.jp/en/index.html
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Professor Shinya Kuroda
Department of Biological Sciences, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 133-8654, JAPAN
Tel: 03-5841-4699
Email: skuroda@bs.s.u-tokyo.ac.jp
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Journal
Science Signaling