Evidence map›Paper›PMID 31741222›Full record

ReviewCurrent osteoporosis reports2019

Exosomes and Extracellular RNA in Muscle and Bone Aging and Crosstalk.

Weiping Qin, Sarah L Dallas

Abstract readReview
In one paragraph

Review in Current osteoporosis reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Roles of skeletal muscle-derived exosomes in osteoporosis.Journal of translational medicine · 2025
    Review
  11. Review
  12. Review
  13. The systemic costs of hematopoietic stem cell aging.Development (Cambridge, England) · 2025
    Review
  14. Review
  15. Review
  16. Review
  17. Bone and muscle crosstalk in ageing and disease.Nature reviews. Endocrinology · 2025
    Review
  18. Review
  19. Molecular communication from bone to skeletal muscle: an overview.Frontiers in cell and developmental biology · 2025
    Review
  20. 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

2 authors.

Weiping QinNational Center for the Medical Consequences of Spinal Cord Injury, James J. Peters Veterans Affairs Medical Center, Bronx, New York, NY, 10468, USA.
Sarah L DallasDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri Kansas City, 650 E. 25th Street, Kansas City, MO, 64108, USA. dallass@umkc.edu.ORCID 0000-0002-5197-891X

Funding

Transgenic and Mechanical Loading CoreP01AG039355 · NIA · UNIVERSITY OF MISSOURI KANSAS CITY · PI BONEWALD, LYNDA F · 2012 to 2024
$19.3M
Leica TCS Sp8 MP Multiphoton MicroscopeS10OD021665 · OD · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2016 to 2016
$600k
Zeiss LSM 710 Confocal Microscopy System for Imaging of Mineralized TissuesS10RR027668 · NCRR · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2011 to 2011
$446k
Extracellular Vesicle Mediated Cell-Cell Communication in BoneR21AR071563 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DALLAS, SARAH L · 2017 to 2018
$377k
Targeting Nanotherapeutics for Neuroprotection after Acute Spinal Cord InjuryR21NS111393 · NINDS · BRONX VETERANS MEDICAL RESEARCH FDN · PI QIN, WEIPING · 2020 to 2020
$359k
Novel Pharmacological and Non-pharmacological Interventions for Bone Loss in SCII01RX002089 · VA · JAMES J PETERS VA MEDICAL CENTER · PI QIN, WEIPING · 2017 to 2023
–
NCRR NIH HHS S10 RR027668NIAMS NIH HHS R21 AR071563NIA NIH HHS P01 AG039355NIH HHS S10 OD021665NINDS NIH HHS R21 NS111393RRD VA I01 RX002089
6 · The paper itself

Abstract

purpose of reviewExtracellular vesicles (EV), which include exosomes and microvesicles, are membrane-bound particles shed by most cell types and are important mediators of cell-cell communication by delivering their cargo of proteins, miRNA, and mRNA to target cells and altering their function. Here, we provide an overview of what is currently known about EV composition and function in bone and muscle cells and discuss their role in mediating crosstalk between these two tissues as well as their role in musculoskeletal aging. RECENT

findingsRecent studies have shown that muscle and bone cells produce EV, whose protein, mRNA, and miRNA cargo reflects the differentiated state of the parental cells. These EV have functional effects within their respective tissues, but evidence is accumulating that they are also shed into the circulation and can have effects on distant tissues. Bone- and muscle-derived EV can alter the differentiation and function of bone and muscle cells. Many of these effects are mediated via small microRNAs that regulate target genes in recipient cells. EV-mediated signaling in muscle and bone is an exciting and emerging field. While considerable progress has been made, much is still to be discovered about the mechanisms regulating EV composition, release, uptake, and function in muscle and bone. A key challenge is to understand more precisely how exosomes function in truly physiological settings.

Indexed as

AgingAnimalsBone and BonesCell CommunicationExosomesExtracellular VesiclesHumansMicroRNAsMuscle Fibers, SkeletalMuscle, SkeletalOsteoblastsOsteoclastsOsteocytesRNARNA, MessengerMicroRNAsRNARNA, MessengerAgingBoneCrosstalkExosomesmiRNAMuscle

Identifiers

PMID31741222
PMCPMC7083338

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.