Evidence map›Paper›PMID 30337682›Full record

ArticleScientific reports2018

Surfactant protein D attenuates acute lung and kidney injuries in pneumonia-induced sepsis through modulating apoptosis, inflammation and NF-κB signaling.

Juan Du, Osama Abdel-Razek, Qiao Shi, Fengqi Hu, Guohua Ding, Robert N Cooney, Guirong Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

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  12. Mitochondria of lung venular capillaries mediate lung-liver cross talk in pneumonia.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
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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

7 authors at 2 institutions in 2 countries.

Juan DuDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA.
Osama Abdel-RazekDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA.
Qiao ShiDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA.
Fengqi HuDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA.
Guohua DingDepartment of Nephrology, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, People's Republic of China.
Robert N CooneyDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA.
Guirong WangDepartment of Surgery, SUNY Upstate Medical University, Syracuse, New York, 13210, USA. wangg@upstate.edu.ORCID http://orcid.org/0000-0002-3288-8572
SUNY Upstate Medical University · USWuhan University · CN

Funding

Mechanisms of differential susceptibility of human SP-B genetic variants to pneumonia and lung injuryR01HL136706 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI WANG, GUIRONG · 2017 to 2020
$1.6M
Mechanisms of 5'UTR splicing of human surfactant protein (SP)-A1 and SP-A2R21HL096007 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI WANG, GUIRONG · 2010 to 2011
$427k
NHLBI NIH HHS R01 HL136706NHLBI NIH HHS R21 HL096007
6 · The paper itself

Abstract

Pneumonia and sepsis are major risk factors for acute kidney injury (AKI). Patients with pneumonia and AKI are at increased risk for morbidity and mortality. Surfactant protein D (SP-D) expressed in lung and kidney plays important roles in innate immunity. However, little is known about the role of organ-specific SP-D in the sepsis. The current study uses wild type (WT), SP-D knockout (KO), and humanized SP-D transgenic (hTG, lung-specific SP-D expression) mice to study organ-specific role of SP-D in pneumonia-induced sepsis. Analyses demonstrated differential lung and kidney injury among three-type mice infected with Pseudomonas aeruginosa. After infection, KO mice showed higher injurious scores in both lung and kidney, and decreased renal function than WT and hTG mice. hTG mice exhibited comparable lung injury but more severe kidney injury compared to WT mice. Increased renal tubular apoptosis, NF-κB activation and proinflammatory cytokines in the kidney of KO mice were found when compared with WT and hTG mice. Furthermore, in vitro primary proximal tubular epithelial cells from KO mice showed more apoptosis with higher level of activated caspase-3 than those from WT mice after LPS treatment. Collectively, SP-D attenuates AKI in the sepsis by modulating renal apoptosis, inflammation and NF-κB signaling.

Indexed as

ApoptosisAcute Kidney InjuryAcute Lung InjuryAnimalsImmunity, InnateInflammationMaleMiceMice, Inbred C57BLMice, KnockoutNF-kappa BPneumoniaPulmonary Surfactant-Associated Protein DSepsisSignal TransductionNF-kappa BPulmonary Surfactant-Associated Protein D

Identifiers

PMID30337682
PMCPMC6193952
OpenAlexW2896818603

What OpenQuestion holds

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Registered trials

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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.