Evidence map›Paper›PMID 27464894›Full record

ArticleScientific reports2016

Hepatic immunophenotyping for streptozotocin-induced hyperglycemia in mice.

Young-Sun Lee, Hyuk Soo Eun, So Yeon Kim, Jong-Min Jeong, Wonhyo Seo, Jin-Seok Byun, Won-Il Jeong, Hyon-Seung Yi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  5. Article
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  11. Local and Systemic Immune Dysregulation Alters Glioma Growth in Hyperglycemic Mice.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  15. Experimental Applications ofMolecules and cells · 2019
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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 at 4 institutions in 1 country.

Young-Sun LeeDepartment of Internal Medicine, Korea University College of Medicine, Seoul 136-705, Republic of Korea.
Hyuk Soo EunDepartment of Internal Medicine, Chungnam National University School of Medicine, Daejeon 305-764, Republic of Korea.
So Yeon KimLaboratory of Liver Research, Biomedical Science and Engineering Interdisciplinary program, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Jong-Min JeongLaboratory of Liver Research, Biomedical Science and Engineering Interdisciplinary program, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Wonhyo SeoLaboratory of Liver Research, Biomedical Science and Engineering Interdisciplinary program, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Jin-Seok ByunDepartment of Oral Medicine, School of Dentistry, Kyungpook National University, Daegu 41566, Republic of Korea.
Won-Il JeongLaboratory of Liver Research, Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
Hyon-Seung YiDepartment of Internal Medicine, Chungnam National University School of Medicine, Daejeon 305-764, Republic of Korea.
Korea Advanced Institute of Science and Technology · KRChungnam National University · KRKorea University · KRKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence revealed that diabetes induces abnormal immune responses that result in serious complications in organs. However, the effect of hyperglycemia on hepatic immunity remains obscure. We evaluated the population and function of hepatic immune cells in streptozotocin (STZ)-induced hyperglycemic mice. CC chemokine receptor 2 (CCR2)-knockout mice and mice with a depletion of regulatory T cells (DEREG) were used to investigate the migration and role of regulatory T cells (Tregs) in hyperglycemic mice. The inflammatory cytokines and hepatic transaminase levels were significantly increased in the hyperglycemic mice. The population and number of infiltrating monocytes, granulocytes, and Tregs were enhanced in the livers of the hyperglycemic mice. Hepatic monocytes other than macrophages showed the increased expression of inflammatory cytokines and chemokines in the hyperglycemic mice. The CCR2 knockout and DEREG chimeric mice exhibited increased populations of activated T cells and neutrophils compared to the WT chimeric mice, which promoted hepatic inflammation in the hyperglycemic mice. The migration of CCR2 knockout Tregs into the liver was significantly reduced compared to the WT Tregs. We demonstrated that hyperglycemia contributes to increase in infiltrating monocytes and Tregs, which are associated with hepatic immune dysfunction in mice. CCR2-mediated migration of Tregs regulates hyperglycemia-induced hepatic inflammation.

Indexed as

ImmunophenotypingAnimalsCytokinesDiabetes Mellitus, ExperimentalGranulocytesLiverMice, KnockoutMice, ObeseMonocytesPhagocytesT-Lymphocytes, RegulatoryCytokines

Identifiers

PMID27464894
PMCPMC4964583
OpenAlexW2479340653

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.