Evidence map›Paper›PMID 33552047›Full record

ArticleFrontiers in immunology2020

Tropomodulin1 Expression Increases Upon Maturation in Dendritic Cells and Promotes Their Maturation and Immune Functions.

Xianmei Liu, Xue Xia, Xifu Wang, Jing Zhou, Lanping Amy Sung, Jinhua Long, Xueyu Geng, Zhu Zeng, Weijuan Yao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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  12. Selenium can regulate the differentiation and immune function of human dendritic cells.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2021
    Article
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

9 authors at 4 institutions in 2 countries.

Xianmei LiuSchool of Basic Medical Sciences, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Xue XiaSchool of Basic Medical Sciences, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Xifu WangDepartment of Emergency, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jing ZhouHemorheology Center, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Lanping Amy SungDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States.
Jinhua LongSchool of Basic Medical Sciences, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Xueyu GengHemorheology Center, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Zhu ZengSchool of Basic Medical Sciences, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Weijuan YaoHemorheology Center, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Peking University · CNGuiyang Medical University · CNBeijing Anzhen Hospital · CNLa Jolla Bioengineering Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are the most potent antigen-presenting cells. Upon maturation, DCs express costimulatory molecules and migrate to the lymph nodes to present antigens to T cells. The actin cytoskeleton plays key roles in multiple aspects of DC functions. However, little is known about the mechanisms and identities of actin-binding proteins that control DC maturation and maturation-associated functional changes. Tropomodulin1 (Tmod1), an actin-capping protein, controls actin depolymerization and nucleation. We found that Tmod1 was expressed in bone marrow-derived immature DCs and was significantly upregulated upon lipopolysaccharide (LPS)-induced DC maturation. By characterizing LPS-induced mature DCs (mDCs) from Tmod1 knockout mice, we found that compared with

Indexed as

AnimalsCell DifferentiationDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalMiceMice, Inbred C57BLMice, KnockoutSignal TransductionTropomodulinTmod1 protein, mouseTropomodulinantigen presentationdendritic cellsmaturationTLR4 signalingTmod1

Identifiers

PMID33552047
PMCPMC7856346
OpenAlexW3118292573

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.