Evidence map›Paper›PMID 28822916›Full record

ArticleRedox biology2017

Wip1-dependent modulation of macrophage migration and phagocytosis.

Yiting Tang, Bing Pan, Xin Zhou, Kai Xiong, Qian Gao, Lei Huang, Ying Xia, Ming Shen, Shulin Yang, Honglin Liu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

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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

15 authors at 8 institutions in 3 countries.

Yiting TangState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Bing PanThe Institute of Cardiovascular Sciences and Institute of Systems Biomedicine, School of Basic Medical Sciences, and Key Laboratory of Molecular Cardiovascular Sciences of Ministry of Education, Peking University Health Science Center, Beijing 100191, China.
Xin ZhouCell Genetics and Developmental Biology, College of Life Sciences, Shaanxi Normal University, Xi'an 710062, China.
Kai XiongDepartment of Veterinary Clinical and Animal Sciences, University of Copenhagen, Grønnegårdsvej 7, 1870 Frederiksberg C, Denmark.
Qian GaoState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Lei HuangState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Ying XiaState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Ming ShenCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Shulin YangState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Honglin LiuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Tao TanDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, United States.
Jianjie MaDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, United States.
Xuehong XuCell Genetics and Developmental Biology, College of Life Sciences, Shaanxi Normal University, Xi'an 710062, China.
Yulian MuState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China. Electronic address: mouyulian@caas.cn.
Kui LiState Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China. Electronic address: likui@caas.cn.
Chinese Academy of Agricultural Sciences · CNNanjing Agricultural University · CNShaanxi Normal University · CNInstitute of Animal Sciences · CNLung Institute · USPeking University · CNThe Ohio State University · USUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage accumulation within the vascular wall is a hallmark of atherosclerosis. Controlling macrophage conversion into foam cells remains a major challenge for treatment of atherosclerotic diseases. Here, we show that Wip1, a member of the PP2C family of Ser/Thr protein phosphatases, modulates macrophage migration and phagocytosis associated with atherosclerotic plaque formation. Wip1 deficiency increases migratory and phagocytic activities of the macrophage under stress conditions. Enhanced migration of Wip1

Indexed as

ChemotaxisPhagocytosisAnimalsCD36 AntigensCells, CulturedMacrophages, PeritonealMiceMice, Inbred C57BLNeuropeptidesPhosphatidylinositol 3-KinasesProtein Phosphatase 2CProto-Oncogene Proteins c-aktrac1 GTP-Binding ProteinCD36 AntigensNeuropeptidesPhosphatidylinositol 3-KinasesPpm1d protein, mouseProtein Phosphatase 2CProto-Oncogene Proteins c-aktrac1 GTP-Binding ProteinRac1 protein, mouse

Identifiers

PMID28822916
PMCPMC5562178
OpenAlexW2744930295

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.