Evidence map›Paper›PMID 25993317›Full record

ArticleKidney international2015

Phospholipase A2 inhibits cisplatin-induced acute kidney injury by modulating regulatory T cells by the CD206 mannose receptor.

Hyunseong Kim, Hyojung Lee, Gihyun Lee, Hyunil Jang, Sung-Su Kim, Heera Yoon, Geun-Hyung Kang, Deok-Sang Hwang, Sun Kwang Kim, Hwan-Suck Chung and 1 more

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In one paragraph

Article in Kidney international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
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  5. Mannose Ligands for Mannose Receptor Targeting.International journal of molecular sciences · 2024
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  7. Pharmacological properties and therapeutic potential of honey bee venom.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Review
  8. Review
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  10. 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

11 authors at 1 institution in 1 country.

Hyunseong KimDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Hyojung LeeDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Gihyun LeeDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Hyunil JangDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Sung-Su KimSoram Korean Medicine Hospital, Gangnam-gu, Seoul, Republic of Korea.
Heera YoonDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Geun-Hyung KangDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Deok-Sang HwangDepartment of Obstetrics and Gynecology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Sun Kwang KimDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Hwan-Suck ChungCancer Preventive Material Development Research Center, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Hyunsu BaeDepartment of Physiology, College of Korean Medicine, Kyung Hee University, Dongdaemoon-gu, Seoul, Republic of Korea.
Kyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we found that Foxp3-expressing CD4(+) regulatory T (Treg) cells attenuate cisplatin-induced acute kidney injury in mice and that bee venom and its constituent phospholipase A2 (PLA2) are capable of modulating Treg cells. Here we tested whether PLA2 could inhibit cisplatin-induced acute kidney injury. As a result of treatment with PLA2, the population of Treg cells was significantly increased, both in vivo and in vitro. PLA2-injected mice showed reduced levels of serum creatinine, blood urea nitrogen, renal tissue damage, and pro-inflammatory cytokine production upon cisplatin administration. These renoprotective effects were abolished by depletion of Treg cells. Furthermore, PLA2 bound to CD206 mannose receptors on dendritic cells, essential for the PLA2-mediated protective effects on renal dysfunction. Interestingly, PLA2 treatment increased the secretion of IL-10 in the kidney from normal mice. Foxp3(+)IL-10(+) cells and CD11c(+)IL-10(+) cells were increased by PLA2 treatment. The anticancer effects of repeated administrations of a low dose of cisplatin were not affected by PLA2 treatment in a tumor-bearing model. Thus, PLA2 may prevent inflammatory responses in cisplatin-induced acute kidney injury by modulating Treg cells and IL-10 through the CD206 mannose receptor.

Indexed as

Antineoplastic AgentsCisplatinAcute Kidney InjuryAnimalsAnti-Inflammatory AgentsCells, CulturedCytoprotectionDisease Models, AnimalDose-Response Relationship, DrugInflammation MediatorsInterleukin-10KidneyLectins, C-TypeLymphocyte ActivationLymphomaMaleAnti-Inflammatory AgentsAntineoplastic AgentsCisplatinIL10 protein, mouseInflammation MediatorsInterleukin-10Lectins, C-TypeMannose-Binding LectinsMannose ReceptorPhospholipases A2Receptors, Cell Surface

Identifiers

PMID25993317
OpenAlexW1495425614

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.