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Verfasst von:Garcia Cortizo, Fabiola [VerfasserIn]   i
 Pfaff, Daniel [VerfasserIn]   i
 Wirth, Angela [VerfasserIn]   i
 Schlotterer, Andrea [VerfasserIn]   i
 Medert, Rebekka [VerfasserIn]   i
 Morgenstern, Jakob [VerfasserIn]   i
 Weber, Tobias [VerfasserIn]   i
 Hammes, Hans-Peter [VerfasserIn]   i
 Fleming, Thomas [VerfasserIn]   i
 Nawroth, Peter Paul [VerfasserIn]   i
 Freichel, Marc [VerfasserIn]   i
 Teleman, Aurelio A. [VerfasserIn]   i
Titel:The activity of glyoxylase 1 is regulated by glucose-responsive phosphorylation on Tyr136
Verf.angabe:Fabiola Garcia Cortizo, Daniel Pfaff, Angela Wirth, Andrea Schlotterer, Rebekka Medert, Jakob Morgenstern, Tobias Weber, Hans-Peter Hammes, Thomas Fleming, Peter Paul Nawroth, Marc Freichel, Aurelio A. Teleman
Jahr:2022
Umfang:11 S.
Fussnoten:Available online 25 November 2021 ; Gesehen am 13.09.2022
Titel Quelle:Enthalten in: Molecular metabolism
Ort Quelle:Oxford [u.a.] : Elsevier, 2012
Jahr Quelle:2022
Band/Heft Quelle:55(2022) vom: Jan., Artikel-ID 101406, Seite 1-11
ISSN Quelle:2212-8778
Abstract:Objective - Methylglyoxal (MG) is a highly reactive α-oxoaldehyde that glycates proteins. MG has been linked to the development of diabetic complications: MG is the major precursor of advanced glycation end products (AGEs), a risk marker for diabetic complications in humans. Furthermore, flies and fish with elevated MG develop insulin resistance, obesity, and hyperglycemia. MG is detoxified in large part through the glyoxalase system, whose rate-limiting enzyme is glyoxalase I (Glo1). Hence, we aimed to study how Glo1 activity is regulated. - Methods - We studied the regulation and effect of post-translational modifications of Glo1 in tissue culture and in mouse models of diabetes. - Results - We show that Glo1 activity is promoted by phosphorylation on Tyrosine 136 via multiple kinases. We find that Glo1 Y136 phosphorylation responds in a bimodal fashion to glucose levels, increasing in cell culture from 0 mM to 5 mM (physiological) glucose, and then decreasing at higher glucose concentrations, both in cell culture and in mouse models of hyperglycemia. - Conclusions - These data, together with published findings that elevated MG leads to hyperglycemia, suggest the existence of a deleterious positive feedback loop whereby hyperglycemia leads to reduced Glo1 activity, contributing to elevated MG levels, which in turn promote hyperglycemia. Hence, perturbations elevating either glucose or MG have the potential to start an auto-amplifying feedback loop contributing to diabetic complications.
DOI:doi:10.1016/j.molmet.2021.101406
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.molmet.2021.101406
 Volltext: https://www.sciencedirect.com/science/article/pii/S2212877821002647
 DOI: https://doi.org/10.1016/j.molmet.2021.101406
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Diabetes
 Glyoxalase
 Phosphorylation
K10plus-PPN:1816505064
Verknüpfungen:→ Zeitschrift

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