Evidence map›Paper›PMID 31129811›Full record

ArticleEndocrine2019

Mir-494 inhibits osteoblast differentiation by regulating BMP signaling in simulated microgravity.

WeiWei Qin, Li Liu, YongChun Wang, Zhe Wang, AnGang Yang, Tao Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Microrna Expression inMicroRNA (Shariqah, United Arab Emirates) · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. [Research Progress in the Regulatory Role of circRNA-miRNA Network in Bone Remodeling].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Review
  9. International journal of molecular sciences · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Mouse Digit Tip Regeneration Is Mechanical Load Dependent.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Long non-coding RNA MALAT1 enhances angiogenesis during bone regeneration by regulating the miR-494/SP1 axis.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  20. Spaceflight Induced Disorders: Potential Nutritional Countermeasures.Frontiers in bioengineering and biotechnology · 2021
    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

6 authors at 2 institutions in 1 country.

WeiWei QinDepartment of Hematology, Tangdu Hospital, Fourth Military Medical University, 710038, Xi'an, China.
Li LiuDepartment of Hematology, Tangdu Hospital, Fourth Military Medical University, 710038, Xi'an, China.
YongChun WangDepartment of Aerospace Biodynamics, School of Aerospace Medicine, Fourth Military Medical University, 710032, Xi'an, China.
Zhe WangDepartment of Nuclear Medicine, Xijing Hospital, Fourth Military Medical University, 710032, Xi'an, China.
AnGang YangDepartment of Immunology, Fourth Military Medical University, 710032, Xi'an, China. agyang@fmmu.edu.cn.
Tao WangDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, 710032, Xi'an, China. wangt@fmmu.edu.cn.
Air Force Medical University · CNXijing Hospital · CN

Funding

National Natural Science Foundation of China 81400110National Natural Science Foundation of China 81472633National Natural Sciences Foundation of China 81773003
6 · The paper itself

Abstract

Although the BMPR-SMAD-RUNX2 signaling pathway plays widely recognized roles in BMP-induced osteogenesis, factors regulating this pathway remain to be defined. In this study, we used simulated microgravity models, which represent mechanical unloading conditions, to detect miRNAs that function in osteoblast differentiation. We found that miR-494 was persistently increased in C2C12 cells subjected to clinorotation conditions and in osteoblasts isolated from tail-suspended rats. Experiments showed that the overexpression of miR-494 correlated with a marked reduction in osteoblast differentiation genes and a decrease in osteogenesis in BMP2-induced osteogenetic differentiation. In contrast, the inhibition of miR-494 promoted BMP2-induced osteogenesis and partially rescued osteoblast differentiation disorder under simulated microgravity conditions. Mechanism studies revealed that miR-494 directly targeted BMPR2 and RUNX2, both of which play vital roles in the BMPR-SMAD-RUNX2 signaling pathway. More importantly, we demonstrated a positive feedback loop between miR-494 and MYOD, a critical transcription factor for myogenesis, indicating that miR-494 may participate in deciding cell fate of the multipotent mesenchymal stem cells (MSCs). Collectively, our study reveals an important role for miR-494 in regulating osteogenesis, the identification of which not only clarifies a regulator of BMP2-induced osteoblast differentiation, but also offers a possible strategy for preventing bone loss under microgravity conditions.

Indexed as

OsteogenesisWeightlessnessAnimalsBone Morphogenetic Protein 2Bone Morphogenetic Protein Receptors, Type IICell DifferentiationCore Binding Factor Alpha 1 SubunitGene Expression ProfilingHEK293 CellsHumansMiceMicroRNAsMyoD ProteinOligonucleotide Array Sequence AnalysisOsteoblastsUp-RegulationBmp2 protein, mouseBmpr2 protein, mouseBone Morphogenetic Protein 2Bone Morphogenetic Protein Receptors, Type IICore Binding Factor Alpha 1 SubunitMicroRNAsMirn494 microRNA, mouseMyoD ProteinRunx2 protein, mouseBMP2miRNAOsteoblast differentiationOsteogenesisSimulated microgravity

Identifiers

PMID31129811
OpenAlexW2999546232

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.