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Erschienen in: Journal of Diabetes & Metabolic Disorders 2/2020

18.06.2020 | Research article

Mechanistic dissection of diabetic retinopathy using the protein-metabolite interactome

verfasst von: Ambrose Teru Patrick, Weilue He, Joshua Madu, Srinivas R. Sripathi, Seulggie Choi, Kook Lee, Faith Pwaniyibo Samson, Folami L. Powell, Manuela Bartoli, Donghyun Jee, Diana R. Gutsaeva, Wan Jin Jahng

Erschienen in: Journal of Diabetes & Metabolic Disorders | Ausgabe 2/2020

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Abstract

Purpose

The current study aims to determine the molecular mechanisms of diabetic retinopathy (DR) using the protein-protein interactome and metabolome map. We examined the protein network of novel biomarkers of DR for direct (physical) and indirect (functional) interactions using clinical target proteins in different models.

Methods

We used proteomic tools including 2-dimensional gel electrophoresis, mass spectrometry analysis, and database search for biomarker identification using in vivo murine and human model of diabetic retinopathy and in vitro model of oxidative stress. For the protein interactome and metabolome mapping, various bioinformatic tools that include STRING and OmicsNet were used.

Results

We uncovered new diabetic biomarkers including prohibitin (PHB), dynamin 1, microtubule-actin crosslinking factor 1, Toll-like receptor (TLR 7), complement activation, as well as hypothetical proteins that include a disintegrin and metalloproteinase (ADAM18), vimentin III, and calcium-binding C2 domain-containing phospholipid-binding switch (CAC2PBS) using a proteomic approach. Proteome networks of protein interactions with diabetic biomarkers were established using known DR-related proteome data. DR metabolites were interconnected to establish the metabolome map. Our results showed that mitochondrial protein interactions were changed during hyperglycemic conditions in the streptozotocin-treated murine model and diabetic human tissue.

Conclusions

Our interactome mapping suggests that mitochondrial dysfunction could be tightly linked to various phases of DR pathogenesis including altered visual cycle, cytoskeletal remodeling, altered lipid concentration, inflammation, PHB depletion, tubulin phosphorylation, and altered energy metabolism. The protein-metabolite interactions in the current network demonstrate the etiology of retinal degeneration and suggest the potential therapeutic approach to treat DR.
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Metadaten
Titel
Mechanistic dissection of diabetic retinopathy using the protein-metabolite interactome
verfasst von
Ambrose Teru Patrick
Weilue He
Joshua Madu
Srinivas R. Sripathi
Seulggie Choi
Kook Lee
Faith Pwaniyibo Samson
Folami L. Powell
Manuela Bartoli
Donghyun Jee
Diana R. Gutsaeva
Wan Jin Jahng
Publikationsdatum
18.06.2020
Verlag
Springer International Publishing
Erschienen in
Journal of Diabetes & Metabolic Disorders / Ausgabe 2/2020
Elektronische ISSN: 2251-6581
DOI
https://doi.org/10.1007/s40200-020-00570-9

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