Evidence map›Paper›PMID 30900683›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Glomerular Proteomic Profiles in the NZB/W F1 Hybrid Mouse Model of Lupus Nephritis.

Liu Xue, Tian Shuyan, Li Xiaoli, Li Zilong, Fan Qiuling, Wang Lining, Li Yanqiu, Yao Li

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Liu XueDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Tian ShuyanDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Li XiaoliDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Li ZilongDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Fan QiulingDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Wang LiningDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Li YanqiuDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Yao LiDepartment of Nephrology, The First Hospital of China Medical University, Shenyang, Liaoning, China (mainland).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Lupus nephritis is one of the most serious complications of systemic lupus erythematosus (SLE) and is associated with patient mortality. This study aimed to investigate the proteomic profiles of the glomerulus in the NZB/W F1 hybrid mouse model of mild and severe lupus nephritis using two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) combined with matrix-assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF-MS). MATERIAL AND METHODS Female NZB/WF1 mice (n=60) at 28 weeks of age were divided into the mild proteinuria group (+1), the moderate proteinuria group (+2), and the severe proteinuria group (+3) using paper strip urine testing, and then later divided into a mild (≤1+) and severe (≥3+) proteinuria group to allow comparison of upregulation and down-regulation of proteins between the two groups. Renal glomeruli were isolated following renal perfusion with magnetic beads. Protein expression was determined by Western blot, immunohistochemistry, 2D-DIGE, and MALDI-TOF-MS. RESULTS A total of 56 differentially expressed proteins were identified from 133 protein spots, of which 18 were upregulated and 23 were down-regulated between groups 1 and 2. Expression of the proteins Ras-related GTP-binding protein B (RRAGB), serine/threonine-protein kinase 1 (SMG1), angiopoietin 2 (ANGP2), methylmalonate semialdehyde (MMSA), and ATP beta chain (ATPB) were identified by Western blot and SMG1, ANGP2, and MMSA were identified by immunohistochemistry. CONCLUSIONS In a mouse model of lupus nephritis, expression of SMG1, MMSA, and ATPB were down-regulated, and RRAGB and ANGP2 were upregulated.

Indexed as

Angiopoietin-2AnimalsBlotting, WesternDisease Models, AnimalFemaleGene Expression ProfilingImmunohistochemistryKidneyKidney DiseasesKidney GlomerulusLupus Erythematosus, SystemicLupus NephritisMethylmalonate-Semialdehyde Dehydrogenase (Acylating)MiceMice, Inbred NZBProteinsAngiopoietin-2Methylmalonate-Semialdehyde Dehydrogenase (Acylating)ProteinsProtein Serine-Threonine KinasesSmg1 protein, mouse

Identifiers

PMID30900683
PMCPMC6698093

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.