Abstract 1199 Neutrophil gelatinase-associated lipocalin (NGAL) promotes calcium oxalate crystallization, growth, aggregation, adhesion to renal cells and invasion through extracellular matrix via its oxalate-binding capability

Neutrophil gelatinase-associated lipocalin (NGAL) is commonly found in the urine of patients with kidney diseases including nephrolithiasis.Nevertheless, its role in stone formation was unknown.Herein, we systematically examined the effects of NGAL on multiple calcium oxalate (CaOx) stonedevelopment processes.Recombinant human NGAL was produced, purified and subjected to crystal assays.The analyses demonstrated that all NGAL concentrations (0.01-10 mg/ ml) concentration-dependently increased the size of CaOx crystals after initial crystallization.At later processes, crystal size expansion, aggregation and adhesion to renal cells were also concentration-dependently induced by NGAL.Additionally, NGAL at all concentrations enhanced extracellular matrix (ECM) invasion by crystals.Mechanistic examinations revealed that NGAL had an affinity to bind oxalate ions without affinity with calcium ions.Finally, the binding of NGAL to CaOx crystal surfaces was confirmed by an immunofluorescence method.In conclusion, our findings indicate that NGAL promotes CaOx stone development by enhancing CaOx crystallization, growth, aggregation, adhesion to renal cells and ECM invasion via its oxalate-binding capability.

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Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.109872
Primary Topic
Acute Kidney Injury Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Abstract 1199 Neutrophil gelatinase-associated lipocalin (NGAL) promotes calcium oxalate crystallization, growth, aggregation, adhesion to renal cells and invasion through extracellular matrix via its oxalate-binding capability

Paleerath Peerapen, Sudarat Hadpech, Chadanat Noonin, Sunisa Yoodee et al.
Journal of Biological Chemistry
Acute Kidney Injury Research
article

Abstract 1199 Neutrophil gelatinase-associated lipocalin (NGAL) promotes calcium oxalate crystallization, growth, aggregation, adhesion to renal cells and invasion through extracellular matrix via its oxalate-binding capability

Paleerath Peerapen, Sudarat Hadpech, Chadanat Noonin, Sunisa Yoodee, Sasinun Detsangiamsak, Visith Thongboonkerd, Somsakul Phuangkham, Suwichaya Chantarasaka, Yanisa Suebsuk
article en

Abstract

Neutrophil gelatinase-associated lipocalin (NGAL) is commonly found in the urine of patients with kidney diseases including nephrolithiasis.Nevertheless, its role in stone formation was unknown.Herein, we systematically examined the effects of NGAL on multiple calcium oxalate (CaOx) stonedevelopment processes.Recombinant human NGAL was produced, purified and subjected to crystal assays.The analyses demonstrated that all NGAL concentrations (0.01-10 mg/ ml) concentration-dependently increased the size of CaOx crystals after initial crystallization.At later processes, crystal size expansion, aggregation and adhesion to renal cells were also concentration-dependently induced by NGAL.Additionally, NGAL at all concentrations enhanced extracellular matrix (ECM) invasion by crystals.Mechanistic examinations revealed that NGAL had an affinity to bind oxalate ions without affinity with calcium ions.Finally, the binding of NGAL to CaOx crystal surfaces was confirmed by an immunofluorescence method.In conclusion, our findings indicate that NGAL promotes CaOx stone development by enhancing CaOx crystallization, growth, aggregation, adhesion to renal cells and ECM invasion via its oxalate-binding capability.

Journal of Biological ChemistryVol. 301(5)
Mahidol University (TH)
National Research Council of Thailand
Zero hunger
Openalex Percentile: Top 84%
Acute Kidney Injury Research
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Abstract 1199 Neutrophil gelatinase-associated lipocalin (NGAL) promotes calcium oxalate crystallization, growth, aggregation, adhesion to renal cells and invasion through extracellular matrix via its oxalate-binding capability — Paleerath Peerapen, Sudarat Hadpech, et al. · Journal of Biological Chemistry (2025) | TGRS Research Map | TGRS