Evidence map›Paper›PMID 39384355›Full record

ArticleKidney research and clinical practice2025

NLRP3 inflammasome activation and macrophage distribution in kidney tissues from patients with acute oxalate nephropathy.

Daorina Bao, Xu Zhang, Su-Xia Wang, Yu Wang, Ming-Hui Zhao

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Article in Kidney research and clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daorina BaoRenal Division, Department of Medicine, Peking University First Hospital, Beijing, China.
Xu ZhangLaboratory of Electron Microscopy, Pathological Centre, Peking University First Hospital, Beijing, China.
Su-Xia WangLaboratory of Electron Microscopy, Pathological Centre, Peking University First Hospital, Beijing, China.
Yu WangRenal Division, Department of Medicine, Peking University First Hospital, Beijing, China.
Ming-Hui ZhaoRenal Division, Department of Medicine, Peking University First Hospital, Beijing, China.

Funding

National Natural Science Foundation of China 81770671National Natural Science Foundation of China 82090021
6 · The paper itself

Abstract

backgroundThe current study was initiated to evaluate renal nucleotide-binding and oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome pathway activation and macrophage subtype distribution and their clinicopathological significance in a cohort of oxalate-induced acute kidney injury.

methodsTwelve patients with biopsy-proven acute oxalate nephropathy (AON) from January 2016 to October 2022 were retrospectively enrolled, with estimated glomerular filtration rate (eGFR)-matched 24 patients with acute tubulointerstitial nephritis (ATIN) as disease control. Pathological lesions as well as markers of NLRP3 inflammasome pathway and macrophage phenotype detected by immunohistochemistry staining were semi-quantitatively analyzed.

resultsOxalate depositions were found in 5% to 20% of tubules with a positive correlation with Sirius Red staining in AON specimens (rp = 0.668, p = 0.02). Disruption of tubular basement membrane and inflammatory cell reaction was more prominent in specimens of AON (both p < 0.05) as compared with ATIN specimens. The expressions of NLRP3, caspase-1, and gasdermin D were significantly increased in AON specimens as well (all p < 0.05). Patients with M1/M2 macrophage ratio <1 were found with more chronic tubulointerstitial lesions and presented with lower eGFR at the last follow-up (24.8 ± 10.6 mL/min/1.73 m2 vs. 55.1 ± 21.2 mL/ min/1.73 m2, p = 0.02) in the AON group.

conclusionThe NLRP3 inflammasome pathway was activated in the kidneys of AON patients, and the ratio of M1 and M2 macrophages was associated with chronicity of pathological changes, which needs further exploration.

Indexed as

CrystalsMacrophagesNLRP3 inflammasomeOxalate nephropathy

Identifiers

PMID39384355
PMCPMC12245602

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