Evidence map›Paper›PMID 41026454›Full record

ArticleCell biochemistry and biophysics2026

Vascular Endothelial cell-derived Exosomal miR-5p-13348_267 Regulates the Fate Determination of Bone Marrow Mesenchymal Stem Cells (BMSCs).

Jiaojiao Wang, Yun Chen, Qiyue Zheng, Wenjie Chen, Yajun Chen, Jieyu He, Yan Xu, Qiong Lu

Abstract read
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In one paragraph

Article in Cell biochemistry and biophysics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Jiaojiao Wang *Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China.
Yun Chen *Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China.
Qiyue ZhengDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China.
Wenjie ChenDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China.
Yajun ChenDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China.
Jieyu HeDepartment of Geriatrics, The Second Xiangya Hospital of Central South University, 139 Middle Renmin Road, Changsha, 410011, Hunan, PR China.
Yan XuDepartment of General Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China. xuyan217@csu.edu.cn.
Qiong LuDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, PR China. christy_luq@csu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis is partially characterized by the shifted differentiation of bone marrow mesenchymal stem cells (BMSCs) towards adipocytes and away from osteoblasts. This study aims to investigate the role of vascular endothelial cell (HMEC-1) exosomes in regulating the osteogenic and adipogenic differentiation of mouse BMSCs, specifically focusing on the involvement of miR-5p-13348_267. Primary BMSCs were cultured under conditions inducing osteogenic or adipogenic differentiation. Alizarin red staining was used to visualize osteogenic mineralized calcium nodules, while oil red O staining was employed to observe lipid droplet formation. MiRNA sequencing was performed to identify miR-5p-13348_267 as a differentially expressed miRNA in HMEC-1 exosomes and HMEC-1 cells. The direct target genes of miR-5p-13348_267 were analyze and filtered by bioinformatics analysis. MiRNA sequencing revealed miR-5p-13348_267 as a key miRNA in HMEC-1 exosomes regulating the differentiation fate of BMSCs. Overexpression of miR-5p-13348_267 significantly enhanced calcium mineralization during osteogenic differentiation of BMSCs and reduced lipid droplet formation during adipogenic differentiation. Overexpressed miR-5p-13348_267 upregulated the expression of osteogenic differentiation-related genes ALP and OC, while downregulating the expression of adipogenic differentiation-related genes mPparg and CD36, as well as the senescence-related gene P16. Bioinformatics analysis identified the top 10 targets of miR-5p-13348_267 involved in regulating the osteogenic-adipogenic differentiation of BMSCs. Our findings suggest that HMEC-1 drived exosomes miR-5p-13348_267 promote the osteogenic differentiation of BMSCs and inhibit their adipogenic differentiation. This mechanism may play a role in slowing down the progression of osteoporosis.

Indexed as

Endothelial CellsExosomesMesenchymal Stem CellsMicroRNAsAdipogenesisAnimalsBone Marrow CellsCell DifferentiationCells, CulturedMiceOsteogenesisMicroRNAsBMSCsLipogenic differentiationmiR-5p-13348_267Osteogenic differentiation

Identifiers

PMID41026454

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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.