Evidence map›Paper›PMID 33161580›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2021

Mechanical loading stimulates bone angiogenesis through enhancing type H vessel formation and downregulating exosomal miR-214-3p from bone marrow-derived mesenchymal stem cells.

Xuetong Wang, Xinle Li, Jie Li, Lidong Zhai, Daquan Liu, Abdusami Abdurahman, Yifan Zhang, Hiroki Yokota, Ping Zhang

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 3 syntheses or guidelines pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  15. PeriostinBone research · 2024
    Article
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  18. Targeting type H vessels in bone-related diseases.Journal of cellular and molecular medicine · 2024
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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

9 authors at 3 institutions in 2 countries.

Xuetong WangDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Xinle LiDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Jie LiDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Lidong ZhaiDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Daquan LiuDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Abdusami AbdurahmanDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Yifan ZhangDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Hiroki YokotaDepartment of Biomedical Engineering, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Ping ZhangDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Tianjin Medical University · CNIndiana University – Purdue University Indianapolis · USUniversity of Indianapolis · US

Funding

MECHANICAL LOADING AND BONER01AR052144 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI YOKOTA, HIROKI · 2006 to 2018
$4.2M
NIAMS NIH HHS R01 AR052144
6 · The paper itself

Abstract

Exosomes are important transporters of miRNAs, which play varying roles in the healing of the bone fracture. Angiogenesis is one of such critical events in bone healing, and we previously reported the stimulatory effect of mechanical loading in vessel remodeling. Focusing on type H vessels and exosomal miR-214-3p, this study examined the mechanism of loading-driven angiogenesis. MiRNA sequencing and qRT-PCR revealed that miR-214-3p was increased in the exosomes of the bone-losing ovariectomized (OVX) mice, while it was significantly decreased by knee loading. Furthermore, compared to the OVX group, exosomes, derived from the loading group, promoted the angiogenesis of endothelial cells. In contrast, exosomes, which were transfected with miR-214-3p, decreased the angiogenic potential. Notably, knee loading significantly improved the microvascular volume, type H vessel formation, and bone mineral density and contents, as well as BV/TV, Tb.Th, Tb.N, and Tb.Sp. In cell cultures, the overexpression of miR-214-3p in endothelial cells reduced the tube formation and cell migration. Collectively, this study demonstrates that knee loading promotes angiogenesis by enhancing the formation of type H vessels and downregulating exosomal miR-214-3p.

Indexed as

Knee JointNeovascularization, PhysiologicAnimalsBone Marrow CellsExosomesFemaleMesenchymal Stem CellsMiceMicroRNAsWeight-BearingMicroRNAsMirn214 microRNA, mouseknee loadingMiRNAosteoporosistype H vesselsvessel remodeling

Identifiers

PMID33161580
PMCPMC7748991
OpenAlexW3102040930

What OpenQuestion holds

Textmetadata
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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.