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oai:uvadoc.uva.es:10324/662742025-09-05T11:48:01Zcom_10324_1134com_10324_931com_10324_894col_10324_1213

Nakamura, Toshifumi c7053d49-8f93-4689-a851-fc153e385180 500 Bonnard, Benjamin 88ef42ed-e38a-460a-bbe4-c07fdf21be44 500 Palacios Ramírez, Roberto d302972e9219ab41 600 0000-0002-0867-1277 Fernández-Celis, Amaya 0c1a8922-55f7-4035-9339-7613ab3218ad 500 Jaisser, Frédéric d8a5843f-d23d-4659-885e-5a125202ace1 500 López-Andrés, Natalia 65f26d7a-7495-40bd-90dc-a5c6dfc02c45 500 2024-02-15T12:48:42Z 2024-02-15T12:48:42Z 2022 Int J Mol Sci. 2022 Jun 15 1422-0067 https://uvadoc.uva.es/handle/10324/66274 10.3390/ijms23126680 6680 12 International Journal of Molecular Sciences 23 1422-0067 Producción Científica The beneficial effects of mineralocorticoid receptor (MR) antagonists (MRAs) for various kidney diseases are established. However, the underlying mechanisms of kidney injury induced by MR activation remain to be elucidated. We recently reported aldosterone-induced enhancement of proteoglycan expression in mitral valve interstitial cells and its association with fibromyxomatous valvular disorder. As the expression of certain proteoglycans is elevated in several kidney diseases, we hypothesized that proteoglycans mediate kidney injury in the context of aldosterone/MR pathway activation. We evaluated the proteoglycan expression and tissue injury in the kidney and isolated glomeruli of uninephrectomy/aldosterone/salt (NAS) mice. The MRA eplerenone was administered to assess the role of the MR pathway. We investigated the direct effects of biglycan, one of the proteoglycans, on macrophages using isolated macrophages. The kidney samples from NAS-treated mice showed enhanced fibrosis and increased expression of biglycan accompanying glomerular macrophage infiltration and enhanced expression of TNF-α, iNOS, Nox2, CCL3 (C-C motif chemokine ligand 3), and phosphorylated NF-κB. Eplerenone blunted these changes. Purified biglycan stimulated macrophages to express TNF-α, iNOS, Nox2, and CCL3. This was prevented by a toll-like receptor 4 (TLR4) or NF-κB inhibitor, indicating that biglycan stimulation is dependent on the TLR4/NF-κB pathway. We identified the proteoglycan biglycan as a novel target of MR involved in MR-induced glomerular injury and macrophage infiltration via a biglycan/TLR4/NF-κB/CCL3 cascade application/pdf eng MDPI info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 Internacional C-C motif chemokine ligand 3 (CCL3) biglycan glomerular injury mineralocorticoid receptor proteoglycan toll-like receptor 4 (TLR4) Biglycan Is a Novel Mineralocorticoid Receptor Target Involved in Aldosterone/Salt-Induced Glomerular Injury info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion https://www.mdpi.com/1422-0067/23/12/6680 SI THUMBNAIL ijms-23-06680-v2-2.pdf.jpg ijms-23-06680-v2-2.pdf.jpg IM Thumbnail image/jpeg 3390 https://uvadoc.uva.es/bitstream/10324/66274/4/ijms-23-06680-v2-2.pdf.jpg 8a62c35933b5142d9b2aeb70816166c0 MD5 4 LICENSE license.txt license.txt text/plain 3929 https://uvadoc.uva.es/bitstream/10324/66274/3/license.txt 289d98c1665ee0d20312360f0e8643c8 MD5 3 CC-LICENSE license_rdf license_rdf application/rdf+xml; charset=utf-8 817 https://uvadoc.uva.es/bitstream/10324/66274/2/license_rdf 975848b171c53b753f7e445c8b5bc0e1 MD5 2 ORIGINAL ijms-23-06680-v2-2.pdf ijms-23-06680-v2-2.pdf application/pdf 4490568 https://uvadoc.uva.es/bitstream/10324/66274/1/ijms-23-06680-v2-2.pdf 897f076bc1bd0b70f9cf9d8fc2094dab MD5 1 10324/66274 oai:uvadoc.uva.es:10324/66274 2025-09-05 13:48:01.081 UVaDOC repositorio@uva.es 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