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pmid:37292142

Irisin Ameliorates Renal Tubulointerstitial Fibrosis by Regulating the Smad4/β-Catenin Pathway in Diabetic Mice.

Zhaohua Yang · Jinying Wei · Yashu Wang · Yunxia Du · Shan Song · Jiawei Li · Ziyuan Su · Yonghong Shi · Haijiang Wu

Diabetes, metabolic syndrome and obesity : targets and therapy · 2023 doi:10.2147/DMSO.S407734

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Irisin Ameliorates Renal Tubulointerstitial Fibrosis by Regulating the Smad4/β-Catenin Pathway in Diabetic Mice.
doi
10.2147/DMSO.S407734
pmid
37292142
authors array · 9 items
[0]
Zhaohua Yang
[1]
Jinying Wei
[2]
Yashu Wang
[3]
Yunxia Du
[4]
Shan Song
[5]
Jiawei Li
[6]
Ziyuan Su
[7]
Yonghong Shi
[8]
Haijiang Wu
journal
Diabetes, metabolic syndrome and obesity : targets and therapy
year
2023
abstract
Background: The primary pathophysiology of diabetic kidney disease (DKD) is tubulointerstitial fibrosis (TIF), and an essential contributing element is excessive extracellular matrix deposition. Irisin is a polypeptide formed by splitting fibronectin type III domain containing 5 (FNDC5), which participates in a number of physiological and pathological processes. Methods: The purpose of this article is to examine irisin's function in DKD and analyze both its in vitro and in vivo effects. The Gene Expression Omnibus (GEO) database was used to download GSE30122, GSE104954, and GSE99325. Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs). The transforming growth factor beta receptor 2 (TGFBR2), irisin, and TGF-β1 were utilized as DEGs to examine the impact of irisin on TIF in diabetic kidney tissue, according to the datasets retrieved from the GEO database and Nephroseq database. Additionally, the therapeutic impact of irisin was also examined using Western blot, RT-qPCR, immunofluorescence, immunohistochemistry, and kits for detecting mouse biochemical indices. Results: In vitro, the findings demonstrated that irisin not only down-regulated the expression of Smad4 and β-catenin but also reduced the expression of proteins linked to fibrosis, the epithelial-mesenchymal transition (EMT), and mitochondrial dysfunction in HK-2 cells maintained in high glucose (HG) environment. In vivo, overexpressed FNDC5 plasmid was injected into diabetic mice to enhance its expression. Our studies found that overexpressed FNDC5 plasmid not only reversed the biochemical parameters and renal morphological characteristics of diabetic mice but also alleviated EMT and TIF by inhibiting Smad4/β-catenin signaling pathway. Conclusion: The above experimental results revealed that irisin could reduce TIF in diabetic mice via regulating the Smad4/β-catenin pathway.
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The GEO database (https://www.ncbi.nlm.nih.gov/geo/) and the Nephroseq database (http://www.nephroseq.org/) were used to generate the data. We value the data platform and the writers who provided the data for upload.
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Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs).
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Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs).
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Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs).
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GSM2641327
sample_count
175
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null
group_sizes_basis
null
platform
19109;19184
taxon
Homo sapiens
title
Transcriptome-based network analysis reveals renal cell type-specific dysregulation of hypoxia-associated transcripts [Tub-FE]
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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gaps array · 6 items
[0]
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[2]
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[3]
asset:data:geo:GSE30122 licence not read
[4]
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[5]
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partial
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[0] object · 10 fields
id
method-1
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differential_expression
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[0]
normalise_counts
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fdr_bh
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count_matrix_with_condition
evidence object · 3 fields
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1
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Each data set is normalized and screened using the limma package of the R programming language (4.0.3, https://www.r-project.org/).
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two_or_more_groups_continuous
evidence object · 3 fields
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[0]
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evidence object · 3 fields
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gaps array · 1 item
[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
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[0] object · 6 fields
capability_id
capability:computational_analysis
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[1]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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blocked_on
nothing:replicable_now
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method object · 5 fields
tier
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normalise_counts
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fdr_bh
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
capability object · 4 fields
tier
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capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 3 items
[0]
GSE30122
[1]
GSE104954
[2]
GSE99325
resolved_accessions array · 3 items
[0]
GSE30122
[1]
GSE104954
[2]
GSE99325
statements array · 1 item
[0]
The GEO database (https://www.ncbi.nlm.nih.gov/geo/) and the Nephroseq database (http://www.nephroseq.org/) were used to generate the data. We value the data platform and the writers who provided the data for upload.
basis
The paper names GSE30122, GSE104954, GSE99325 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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normalise_counts
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[0]
source:pmid:37292142
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run_analysis
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[0]
data:geo:GSE104954
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state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
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minimax
read_at
2026-11-01T18:43:17Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
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14348
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1950
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256
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extraction
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absent
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not_run
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execution.not_run
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pmid:37292142
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paper
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pmid:37292142
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id
source:pmid:37292142
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manuscript
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PMID 37292142 full text
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id
data:geo:GSE104954
type
dataset
label
GEO GSE104954
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
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classification
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type
paper
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pmid:37292142
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source:pmid:37292142
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manuscript
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PMID 37292142 full text
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type
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GEO GSE104954
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agent:corpus-assay-engine
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[3]
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[4]
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[5]
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[6]
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[7]
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[0]
ion in DKD and analyze both its in vitro and in vivo effects. The Gene Expression Omnibus (GEO) d
[1]
maintained in high glucose (HG) environment. In vivo, overexpressed FNDC5 plasmid was injected in
[2]
immunohistochemistry, and kits for detecting mouse biochemical indices. Results: In vitro, the
[3]
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paper_text_order:543
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[0]
tic impact of irisin was also examined using Western blot, RT-qPCR, immunofluorescence, immunohistoche
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irisin was also examined using Western blot, RT-qPCR, immunofluorescence, immunohistochemistry, a
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37292142", "kind": "science-record", "revision": 4, "content_hash": "sha256:9a5c55f6bc84954bc72e6a240f12297adc6e91cfac7951a8b6d3df11b3042807", "created_at": "2026-11-01T19:02:01Z", "updated_at": "2026-11-01T22:52:05Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Irisin Ameliorates Renal Tubulointerstitial Fibrosis by Regulating the Smad4/β-Catenin Pathway in Diabetic Mice.", "doi": "10.2147/DMSO.S407734", "pmid": "37292142", "authors": ["Zhaohua Yang", "Jinying Wei", "Yashu Wang", "Yunxia Du", "Shan Song", "Jiawei Li", "Ziyuan Su", "Yonghong Shi", "Haijiang Wu"], "journal": "Diabetes, metabolic syndrome and obesity : targets and therapy", "year": 2023, "abstract": "Background: The primary pathophysiology of diabetic kidney disease (DKD) is tubulointerstitial fibrosis (TIF), and an essential contributing element is excessive extracellular matrix deposition. Irisin is a polypeptide formed by splitting fibronectin type III domain containing 5 (FNDC5), which participates in a number of physiological and pathological processes.\nMethods: The purpose of this article is to examine irisin's function in DKD and analyze both its in vitro and in vivo effects. The Gene Expression Omnibus (GEO) database was used to download GSE30122, GSE104954, and GSE99325. Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs). The transforming growth factor beta receptor 2 (TGFBR2), irisin, and TGF-β1 were utilized as DEGs to examine the impact of irisin on TIF in diabetic kidney tissue, according to the datasets retrieved from the GEO database and Nephroseq database. Additionally, the therapeutic impact of irisin was also examined using Western blot, RT-qPCR, immunofluorescence, immunohistochemistry, and kits for detecting mouse biochemical indices.\nResults: In vitro, the findings demonstrated that irisin not only down-regulated the expression of Smad4 and β-catenin but also reduced the expression of proteins linked to fibrosis, the epithelial-mesenchymal transition (EMT), and mitochondrial dysfunction in HK-2 cells maintained in high glucose (HG) environment. In vivo, overexpressed FNDC5 plasmid was injected into diabetic mice to enhance its expression. Our studies found that overexpressed FNDC5 plasmid not only reversed the biochemical parameters and renal morphological characteristics of diabetic mice but also alleviated EMT and TIF by inhibiting Smad4/β-catenin signaling pathway.\nConclusion: The above experimental results revealed that irisin could reduce TIF in diabetic mice via regulating the Smad4/β-catenin pathway.", "claims": [{"id": "claim-method", "statement": "Each data set is normalized and screened using the limma package of the R programming language (4.0.3, https://www.r-project.org/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37292142", "locator": "sections[3] \"Bioinformatic Analysis\" paragraph 2", "quote": "Each data set is normalized and screened using the limma package of the R programming language (4.0.3, https://www.r-project.org/)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The GEO database (https://www.ncbi.nlm.nih.gov/geo/) and the Nephroseq database (http://www.nephroseq.org/) were used to generate the data. We value the data platform and the writers who provided the data for upload.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37292142", "locator": "sections[25] \"Data Sharing Statement\" paragraph 2", "quote": "The GEO database (https://www.ncbi.nlm.nih.gov/geo/) and the Nephroseq database (http://www.nephroseq.org/) were used to generate the data. We value the data platform and the writers who provided the data for upload."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs).", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37292142", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Analysis of renal tubule samples from nondiabetic and diabetic mice identified 94 differentially expressed genes (DEGs).", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37292142"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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