Evidence map›Paper›PMID 36593461›Full record

ArticleJournal of nanobiotechnology2023

TiO

Zhaoyue Fu, Yongli Hou, Håvard Jostein Haugen, Xutao Chen, Kang Tang, Liang Fang, Yong Liu, Shu Zhang, Qianli Ma, Lihua Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
16.5field-weighted citation impact, top 1% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 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

10 authors at 3 institutions in 2 countries.

Zhaoyue Fu *Department of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China.
Yongli Hou *Department of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China.
Håvard Jostein HaugenDepartment of Biomaterials, Institute of Clinical Dentistry, University of Oslo, 0317, Oslo, Norway.
Xutao ChenDepartment of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China.
Kang TangDepartment of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China.
Liang FangDepartment of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China.
Yong LiuThe Key Laboratory of Aerospace Medicine, Ministry of Education, Air Force Medical University, Xi'an, 710032, Shaanxi, China.
Shu ZhangThe Key Laboratory of Aerospace Medicine, Ministry of Education, Air Force Medical University, Xi'an, 710032, Shaanxi, China.
Qianli MaDepartment of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China. qianlima@odont.uio.no.
Lihua ChenDepartment of Immunology, School of Basic Medicine, Fourth Military Medical University, 169 West Changle Road, Xi'an, 710032, People's Republic of China. chenlh@fmmu.edu.cn.
Air Force Medical University · CNUniversity of Oslo · NOAir Force Engineering University · CN

Funding

Innovation Capability Support Plan of Shaanxi Province No. 2020TD-041Innovation Capability Support Plan of Shaanxi Province No.BZZ21J002National Natural Science Foundation of China 81971752National Natural Science Foundation of China 82071848
6 · The paper itself

Abstract

backgroundMicrogravity directly disturbs the reorganization of the cytoskeleton, exerting profound effects on the physiological process of macrophages. Although it has been established that macrophage M1/M2 polarization could be manipulated by the surface nanostructure of biomaterial in our previous study under normal gravity, how will inflammatory monocytes (iMos)-derived macrophages respond to diverse nanostructured Ti surfaces under normal gravity or microgravity remains unrevealed.

resultsIn this study, Cytochalasin D, a cytoskeleton relaxant, was employed to establish the simulated microgravity (SMG) environment. Our results showed that human iMos polarized into M2c macrophages on NT5 surface but M1 type on NT20 surface with divergent inflammatory phenotypes according to the profile of macrophage polarization featured molecules under normal gravity. However, such manipulative effects of NTs surfaces on iMos-derived macrophages were strikingly weakened by SMG, characterized by the altered macrophage morphology, changed cytokine secretion profile, and decreased cell polarization capacity.

conclusionsTo our knowledge, this is the first metallic implantable material study focusing on the functions of specific monocyte subsets and its crucial role of the cytoskeleton in materials-mediated host immune response, which enriches our mechanism knowledge about the crosstalk between immunocytes and biomaterials. The results obtained in the present study may also provide potential targets and strategies for biomaterial development and clinical treatment via precise immune-regulation under normal gravity and microgravity.

Indexed as

MonocytesNanostructuresBiocompatible MaterialsCytoskeletonHumansTitaniumBiocompatible MaterialsTitaniumtitanium dioxideCytoskeletonInflammatory monocyte (iMos)Macrophage polarizationSimulated microgravity (SMG)TiO2

Identifiers

PMID36593461
PMCPMC9809010
OpenAlexW4313475882

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.