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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

The macrophage phenotype and inflammasome component NLRP3 contributes to nephrocalcinosis-related chronic kidney disease independent from IL-1-mediated tissue injury

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Author(s):
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Anders, Hans-Joachim [1] ; Suarez-Alvarez, Beatriz [1] ; Grigorescu, Melissa [1] ; Foresto-Neto, Orestes [1] ; Steiger, Stefanie [1] ; Desai, Jyaysi [1] ; Marschner, Julian A. [1] ; Honarpisheh, Mohsen [1] ; Shi, Chongxu [1] ; Jordan, Jutta [2] ; Mueller, Lisa [3] ; Burzlaff, Nicolai [3] ; Baeuerle, Tobias [2] ; Mulay, Shrikant R. [1]
Total Authors: 14
Affiliation:
[1] Ludwig Maximilians Univ Munchen, Klinikum Univ, Med Klin & Poliklin 4, Munich - Germany
[2] Friedrich Alexander Univ Erlangen Nurnberg, Inst Radiol, Preclin Imaging Platform Erlangen, Erlangen - Germany
[3] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, Inorgan Chem & Interdisciplinary Ctr Mol Mat, Erlangen - Germany
Total Affiliations: 3
Document type: Journal article
Source: Kidney International; v. 93, n. 3, p. 656-669, MAR 2018.
Web of Science Citations: 22
Abstract

Primary/secondary hyperoxalurias involve nephrocalcinosis-related chronic kidney disease (CKD) leading to end-stage kidney disease. Mechanistically, intrarenal calcium oxalate crystal deposition is thought to elicit inflammation, tubular injury and atrophy, involving the NLRP3 inflammasome. Here, we found that mice deficient in NLRP3 and ASC adaptor protein failed to develop nephrocalcinosis, compromising conclusions on nephrocalcinosis-related CKD. In contrast, hyperoxaluric wild-type mice developed profound nephrocalcinosis. NLRP3 inhibition using the beta-hydroxybutyrate precursor 1,3-butanediol protected such mice from nephrocalcinosis-related CKD. Interestingly, the IL-1 inhibitor anakinra had no such effect, suggesting IL-1-independent functions of NLRP3. NLRP3 inhibition using 1,3-butanediol treatment induced a shift of infiltrating renal macrophages from pro-inflammatory (CD45(+)F4/80(+)CD11b(+)CX3CR1(+)CD206(-)) and pro-fibrotic (CD45(+)F4/80(+)CD11b(+)CX3CR1(+)CD206(+)TGF beta(+)) to an anti-inflammatory (CD45(+)F4/80(+)CD11b(+)CD206(+)TGF beta(-)) phenotype, and prevented renal fibrosis. Finally, in vitro studies with primary murine fibroblasts confirmed the non-redundant role of NLRP3 in the TGF-beta signaling pathway for fibroblast activation and proliferation independent of the NLRP3 inflammasome complex formation. Thus, nephrocalcinosis-related CKD involves NLRP3 but not necessarily via intrarenal IL-1 release but rather via other biological functions including TGFR signaling and macrophage polarization. Hence, NLRP3 may be a promising therapeutic target in hyperoxaluria and nephrocalcinosis. (AU)

FAPESP's process: 15/24991-1 - The role of Uromodulin in the pathogenesis of diabetic nephropathy
Grantee:Orestes Foresto Neto
Support type: Scholarships abroad - Research Internship - Doctorate (Direct)