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Adult kidney explants is a physiologic model for studying diabetic nephropathy


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Título : Adult kidney explants is a physiologic model for studying diabetic nephropathy
Autor : Gómez Jaramillo, Laura
Cano Cano, Fátima
Campos Caro, Antonio
Alcalá Díaz-Mor, Martín
Álvarez Gallego, Fabiola
Aguilar Diosdado, Manuel
Arroba, Ana I.
Materias: Adult kidney explantsInflammationFibrosisEx vivo model diseaseDiabetic nephropathyCell signalling
Editorial : Elsevier
Citación : Laura Gómez-Jaramillo, Fátima Cano-Cano, Antonio Campos-Caro, Martín Álcala, Fabiola Álvarez-Gallego, Ana I. Arroba, Manuel Aguilar-Diosdado, Adult kidney explants is a physiologic model for studying diabetic nephropathy, Life Sciences, Volume 300, 2022, 120575, ISSN 0024-3205, https://doi.org/10.1016/j.lfs.2022.120575.
Resumen : Inflammatory processes play a central role in the pathogenesis of diabetic nephropathy (DN) in the early stages of the disease. In vitro approach using cell lines help to understand the mechanisms involves and allow the molecular and biochemical processes. Adult kidney (AK) explants remain an essential instrument for advancing our understanding of the molecular and cellular regulation of signalling pathways from an organotipic view with physiological system interaction integrated. AK explants from T1DM animal model (BB rat) are obtained by slicing central kidney area preserving the organ's cytoarchitecture and reproduce the classical events detected during the DN in an in vivo model such as inflammation, epithelial-mesenchymal transition (EMT) processes by the modulation of a-SMA and e-Cadherin among others which have been determined by qRT-PCR, western-blot and immunohistochemistry. In this regard, AK explants reproduce the signalling pathways involve in DN progression (proinflammatory NFkB and inflammasome complex). This work demonstrates AK explants is a physiological experimental approach for studying the development and progression of DN. Furthermore, the inflammatory processes in AK explants under a diabetic environment and/or BB rats could be modulated by potential treatments for DN.
URI : http://hdl.handle.net/10637/14534
Derechos: http://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
openAccess
ISSN : 0024-3205
Fecha de publicación : 25-abr-2022
Centro : Universidad San Pablo-CEU
Aparece en las colecciones: Facultad de Farmacia





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