Please use this identifier to cite or link to this item: https://repositorio.uca.edu.ar/handle/123456789/8705
Título : TRPC proteins contribute to development of diabetic retinopathy and regulate glyoxalase 1 activity and methylglyoxal accumulation
Autor : Sachdeva, Robin 
Schlotterer, Andrea 
Schumacher, Dagmar 
Matka, Christin 
Mathar, Ilka 
Dietrich, Nadine 
Medert, Rebekka 
Kriebs, Ulrich 
Lin, Jihong 
Nawroth, Peter 
Birnbaumer, Lutz 
Fleming, Thomas 
Hammes, Hans-Peter 
Freichel, Marc 
Palabras clave : RETINOPATIA DIABETICAENFERMEDADES METABOLICASHIPERGLUCEMIA
Fecha de publicación : 2018
Editorial : Elsevier
Cita : Sachdeva R, Schlotterer A, Schumacher D, et al. TRPC proteins contribute to development of diabetic retinopathy and regulate glyoxalase 1 activity and methylglyoxal accumulation [en línea]. Molecular Metabolism. 2018;9:156-167. doi:10.1016/j.molmet.2018.01.003 Disponible en:
Resumen : Objective Diabetic retinopathy (DR) is induced by an accumulation of reactive metabolites such as ROS, RNS, and RCS species, which were reported to modulate the activity of cation channels of the TRPC family. In this study, we use Trpc1/4/5/6−/− compound knockout mice to analyze the contribution of these TRPC proteins to diabetic retinopathy. Methods We used Nanostring- and qPCR-based analysis to determine mRNA levels of TRPC channels in control and diabetic retinae and retinal cell types. Chronic hyperglycemia was induced by Streptozotocin (STZ) treatment. To assess the development of diabetic retinopathy, vasoregression, pericyte loss, and thickness of individual retinal layers were analyzed. Plasma and cellular methylglyoxal (MG) levels, as well as Glyoxalase 1 (GLO1) enzyme activity and protein expression, were measured in WT and Trpc1/4/5/6−/− cells or tissues. MG-evoked toxicity in cells of both genotypes was compared by MTT assay. Results: We find that Trpc1/4/5/6−/− mice are protected from hyperglycemia-evoked vasoregression determined by the formation of acellular capillaries and pericyte drop-out. In addition, Trpc1/4/5/6−/− mice are resistant to the STZ-induced reduction in retinal layer thickness. The RCS metabolite methylglyoxal, which represents a key mediator for the development of diabetic retinopathy, was significantly reduced in plasma and red blood cells (RBCs) of STZ-treated Trpc1/4/5/6−/− mice compared to controls. GLO1 is the major MG detoxifying enzyme, and its activity and protein expression were significantly elevated in Trpc1/4/5/6-deficient cells, which led to significantly increased resistance to MG toxicity. GLO1 activity was also increased in retinal extracts from Trpc1/4/5/6−/− mice. The TRPCs investigated here are expressed at different levels in endothelial and glial cells of the retina. Conclusion The protective phenotype in diabetic retinopathy observed in Trpc1/4/5/6−/− mice is suggestive of a predominant action of TRPCs in Müller cells and microglia because of their central position in the retention of a proper homoeostasis of the neurovascular unit.
URI : https://repositorio.uca.edu.ar/handle/123456789/8705
ISSN : 2212-8778
DOI: 10.1016/j.molmet.2018.01.003
Derechos: Atribución-NoComercial-CompartirIgual 4.0 Internacional
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