Elevated Levels of Urinary Extracellular Vesicle Fibroblast-Specific Protein 1 in Patients with Active Crescentic Glomerulonephritis.


Journal

Nephron
ISSN: 2235-3186
Titre abrégé: Nephron
Pays: Switzerland
ID NLM: 0331777

Informations de publication

Date de publication:
2019
Historique:
received: 01 06 2018
accepted: 06 11 2018
pubmed: 13 12 2018
medline: 1 1 2020
entrez: 13 12 2018
Statut: ppublish

Résumé

Extracellular vesicles (EVs), including exosomes, are present in various bodily fluids, including urine. We and others previously reported that cells expressing fibroblast-specific protein 1 (FSP1) accumulate within damaged glomeruli, and that urinary FSP1, as well as urinary soluble CD163, could potentially serve as a biomarker of ongoing glomerular injury. To test that idea, we collected urine samples from 37 patients with glomerular disease; purified the urinary EVs; characterized them using Nanosight, western blotting, and immunoelectron microscopy; and determined FSP1 and soluble CD163 levels using enzyme-linked immunosorbent assays. Deemed to be mainly exosomes based on their size distribution, the EVs in urine contained FSP1, and a portion of the FSP1-positive vesicles was also positive for podocalyxin. FSP1 levels in urinary EVs were (1) positively correlated with rates of biopsy-proven cellular crescent formation (r = 0.562, p < 0.001) and total crescent formation (r = 0.448, p = 0.005) among total glomeruli; (2) significantly higher in patients with cellular crescents affecting 20% or more of their glomeruli than in those with fewer affected glomeruli (p = 0.003); and (3) significantly decreased after glucocorticoid and immunosuppressant therapy (p < 0.05). A positive correlation between FSP1 levels in urinary EVs and urinary soluble CD163 levels was confirmed (r = 0.367, p < 0.05). These data suggest that a portion of urinary FSP1 is secreted as EVs originating from podocytes, and that FSP1 levels reflect active and ongoing glomerular injury and disease activity, such as cellular crescent formation.

Sections du résumé

BACKGROUND/AIMS
Extracellular vesicles (EVs), including exosomes, are present in various bodily fluids, including urine. We and others previously reported that cells expressing fibroblast-specific protein 1 (FSP1) accumulate within damaged glomeruli, and that urinary FSP1, as well as urinary soluble CD163, could potentially serve as a biomarker of ongoing glomerular injury.
METHODS
To test that idea, we collected urine samples from 37 patients with glomerular disease; purified the urinary EVs; characterized them using Nanosight, western blotting, and immunoelectron microscopy; and determined FSP1 and soluble CD163 levels using enzyme-linked immunosorbent assays.
RESULTS
Deemed to be mainly exosomes based on their size distribution, the EVs in urine contained FSP1, and a portion of the FSP1-positive vesicles was also positive for podocalyxin. FSP1 levels in urinary EVs were (1) positively correlated with rates of biopsy-proven cellular crescent formation (r = 0.562, p < 0.001) and total crescent formation (r = 0.448, p = 0.005) among total glomeruli; (2) significantly higher in patients with cellular crescents affecting 20% or more of their glomeruli than in those with fewer affected glomeruli (p = 0.003); and (3) significantly decreased after glucocorticoid and immunosuppressant therapy (p < 0.05). A positive correlation between FSP1 levels in urinary EVs and urinary soluble CD163 levels was confirmed (r = 0.367, p < 0.05).
CONCLUSION
These data suggest that a portion of urinary FSP1 is secreted as EVs originating from podocytes, and that FSP1 levels reflect active and ongoing glomerular injury and disease activity, such as cellular crescent formation.

Identifiants

pubmed: 30540988
pii: 000495217
doi: 10.1159/000495217
doi:

Substances chimiques

Biomarkers 0
Calcium-Binding Proteins 0
S100 Calcium-Binding Protein A4 0
S100A4 protein, human 142662-27-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

177-187

Informations de copyright

© 2018 S. Karger AG, Basel.

Auteurs

Yukie Morikawa (Y)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Naoki Takahashi (N)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan, ntakahas@u-fukui.ac.jp.

Kazuko Kamiyama (K)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Kazuhisa Nishimori (K)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Yudai Nishikawa (Y)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Sayu Morita (S)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Mamiko Kobayashi (M)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Sachiko Fukushima (S)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Seiji Yokoi (S)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Daisuke Mikami (D)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Hideki Kimura (H)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Kenji Kasuno (K)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Tetsuya Yashiki (T)

DS Pharma Biomedical Co., Ltd., Suita, Japan.

Hironobu Naiki (H)

Department of Molecular Pathology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

Masanori Hara (M)

Iwamuro Health Promotion Center, Niigata, Japan.

Masayuki Iwano (M)

Department of Nephrology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.

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