Evidence map›Paper›PMID 31892161›Full record

ArticleInternational journal of molecular sciences2019

The Acute Phase Response Is a Prominent Renal Proteome Change in Sepsis in Mice.

Beáta Róka, Pál Tod, Tamás Kaucsár, Matej Vizovišek, Robert Vidmar, Boris Turk, Marko Fonović, Gábor Szénási, Péter Hamar

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  14. Time-Dependent miRNA Profile during Septic Acute Kidney Injury in Mice.International journal of molecular sciences · 2020
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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

9 authors at 2 institutions in 2 countries.

Beáta RókaInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary.
Pál TodInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary.
Tamás KaucsárInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary.
Matej VizovišekDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.ORCID 0000-0002-3860-1659
Robert VidmarDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.
Boris TurkDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.ORCID 0000-0002-9007-5764
Marko FonovićDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.
Gábor SzénásiInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary.
Péter HamarInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary.
Semmelweis University · HUJožef Stefan Institute · SI

Funding

European Regional Development Fund GINOP 2.3.2-15-2016-00048Hungarian Scientific Research Fund ANN-110810Hungarian Scientific Research Fund SNN-114619Javna Agencija za Raziskovalno Dejavnost RS N1-0031Javna Agencija za Raziskovalno Dejavnost RS P1-0140Kispál Gyula startup grant of the University of Pécs 300021Nemzeti Kutatási, Fejlesztési és Innovaciós Alap NVKP_16-1-2016-0042
6 · The paper itself

Abstract

(1) Background: Sepsis-induced acute kidney injury (AKI) is the most common form of acute kidney injury (AKI). We studied the temporal profile of the sepsis-induced renal proteome changes. (2) Methods: Male mice were injected intraperitoneally with bacterial lipopolysaccharide (LPS) or saline (control). Renal proteome was studied by LC-MS/MS (ProteomeXchange: PXD014664) at the early phase (EP, 1.5 and 6 h after 40 mg/kg LPS) and the late phase (LP, 24 and 48 h after 10 mg/kg LPS) of LPS-induced AKI. Renal mRNA expression of acute phase proteins (APP) was assessed by qPCR. (3) Results: Renal proteome change was milder in EP vs. LP. APPs dominated the proteome in LP (proteins upregulated at least 4-fold (APPs/all): EP, 1.5 h: 0/10, 6 h: 1/10; LP, 24 h: 22/47, 48 h: 17/44). Lipocalin-2, complement C3, fibrinogen, haptoglobin and hemopexin were the most upregulated APPs. Renal mRNA expression preceded the APP changes with peak effects at 24 h, and indicated renal production of the majority of APPs. (4) Conclusions: Gene expression analysis revealed local production of APPs that commenced a few hours post injection and peaked at 24 h. This is the first demonstration of a massive, complex and coordinated acute phase response of the kidney involving several proteins not identified previously.

Indexed as

Acute Kidney InjuryAcute-Phase ProteinsAcute-Phase ReactionAnimalsComplement C3Disease Models, AnimalInterleukin-6KidneyLipopolysaccharidesMaleMiceProteomeSepsisTumor Necrosis Factor-alphaAcute-Phase ProteinsComplement C3Interleukin-6LipopolysaccharidesProteomeTumor Necrosis Factor-alphaacute kidney injury (AKI)acute phase proteins (APP)lipopolysaccharide (LPS)mouserenal acute phase reaction (APR)

Identifiers

PMID31892161
PMCPMC6982205
OpenAlexW2997171323

What OpenQuestion holds

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Registered trials

None linked

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.