Evidence map›Paper›PMID 28695057›Full record

ArticleAmerican journal of clinical and experimental immunology2017

Effects of peritoneal macrophage autophagy on the immune function of sepsis mice.

Da-Long Zhang, Shun-Wen Zhang, Qing Hong Cheng, Fang Wu, Jiang-Dong Wu, Jie Zhang, Jiang-Tao Dong, Hui-Yun Zhu, Shuai Zhang, Qing-Qing Wu and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of clinical and experimental immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-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

8 citing papers in PubMed, 14 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

11 authors at 1 institution in 1 country.

Da-Long ZhangThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Shun-Wen ZhangSchool of Basic Medical Sciences, Nanjing Medical UniversityNanjing 211166, Jiangsu Province, China.
Qing Hong ChengThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Fang WuThe Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathophysiology, School of Medicine, Shihezi University, Collaborative Innovation Center of High Incidence of Zoonoses Communicable Disease Prevention in the Western RegionShihezi 832002, Xinjiang, China.
Jiang-Dong WuThe Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathophysiology, School of Medicine, Shihezi University, Collaborative Innovation Center of High Incidence of Zoonoses Communicable Disease Prevention in the Western RegionShihezi 832002, Xinjiang, China.
Jie ZhangThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Jiang-Tao DongThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Hui-Yun ZhuThe Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathophysiology, School of Medicine, Shihezi University, Collaborative Innovation Center of High Incidence of Zoonoses Communicable Disease Prevention in the Western RegionShihezi 832002, Xinjiang, China.
Shuai ZhangThe Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathophysiology, School of Medicine, Shihezi University, Collaborative Innovation Center of High Incidence of Zoonoses Communicable Disease Prevention in the Western RegionShihezi 832002, Xinjiang, China.
Qing-Qing WuThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Wan-Jiang ZhangThe First Affiliated Hospital, School of Medicine, Shihezi UniversityShihezi 832002, Xinjiang, China.
Shihezi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of peritoneal macrophage autophagy on immune function in sepsis mice.

methodsSeventy-two male BALB/C mice were intraperitoneally injected with LPS to induce sepsis. The mice were randomly divided into six groups: LPS+2 h, LPS+6 h, LPS+12 h, LPS+24 h and LPS+36 h. LPS with a dose of 10 mg/kg was intraperitoneally injected into the abdominal cavity of the sepsis mice, and the control group was injected with the same dose of saline. ELISA was used to detect the concentrations of inflammatory factors IL-2, IL-10 and TNF-α in the peripheral blood, and the CD4+T/CD8+T ratio in the peripheral blood was detected by flow cytometry. The expression levels of LC3II and Beclin-1/beta-action in the mouse macrophages were measured using Western blot to determine the level of autophagy.

resultsThe expression levels of LC3II and Beclin-1 were significantly higher in the peritoneal macrophages of the mice from the LPS+2 h group than in those of the mice from the normal group (P<0.05). Meanwhile, these levels continuously declined in the LPS+6 h, LPS+12 h, LPS+24 h and LPS+36 h groups (P<0.05). The peripheral blood CD4+T/CD8+T cell ratio was significantly higher in the LPS+2 h and LPS+6 h groups than in the normal group (P<0.05). The ratio peaked at 6 h and then continuously declined (P<0.05). Furthermore, the concentrations of IL-2 and Tnf-α were significantly higher in the peripheral blood serum of the LPS+2 h, LPS+6 h and LPS+12 h groups than in those of the normal group (P<0.05). The peak was observed at 12 h followed by a continuous decline in the LPS+24 h and 3 LPS+6 h groups (P<0.05). The peripheral serum IL-10 concentration was significantly higher in the LPS+2 h, LPS+6 h, LPS+12 h, LPS+24 h and LPS+36 h groups than in the normal group (P<0.05). In the LPS+6 h, LPS+12 h, LPS+24 h and LPS+36 h groups, the peritoneal macrophages LC3II, Beclin-1 and peripheral serum CD+4T/CD+8T ratio correlation index R

conclusionAutophagy in peritoneal macrophages plays an important role in the immune function of sepsis mice. In addition, the autophagy of peritoneal macrophages and the immune function of sepsis mice are strongly correlated. Furthermore, macrophage autophagy plays an important role in the immune function changes in sepsis mice, and the underlying mechanism may be involved in inflammation and macrophage antigen presentation by regulating the secretion of inflammatory cytokines and lymphocyte apoptosis antagonism.

Indexed as

autophagy immune function changeMacrophagesepsis disease

Identifiers

PMID28695057
PMCPMC5498851
OpenAlexW2975267186

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.