Evidence map›Paper›PMID 38137532›Full record

ArticleBiomedicines2023

Irisin Enhances Mitochondrial Function in Osteoclast Progenitors during Differentiation.

Eben Estell, Tsunagu Ichikawa, Paige Giffault, Lynda Bonewald, Bruce Spiegelman, Clifford Rosen

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Lactate regulates osteoclastogenesis via H3k18la in osteoarthritis.International journal of molecular medicine · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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 3 institutions in 1 country.

Eben EstellCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME 04074, USA.ORCID 0000-0001-8319-6886
Tsunagu IchikawaCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME 04074, USA.
Paige GiffaultCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME 04074, USA.
Lynda BonewaldDepartment of Anatomy, Cell Biology and Physiology, Orthopaedic Surgery, School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Bruce SpiegelmanDepartment of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Clifford RosenCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME 04074, USA.
MaineHealth · USHarvard University · USIndiana University – Purdue University Indianapolis · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI CLIFFORD JAMES ROSEN · 2017 to 2026
$51.6M
Targeting FSH for the Therapy of Osteoporosis, Obesity and NeurodegenerationU19AG060917 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PENG LIU · 2019 to 2026
$29.0M
The Role of Irisin in Initiating Resorption During the Skeletal Response to ExerciseK01AR081959 · NIAMS · UNIVERSITY OF NEW ENGLAND · PI Eben Grant Estell · 2023 to 2026
$509k
NIAMS NIH HHS 1K01AR081959-01NIAMS NIH HHS K01 AR081959NIA NIH HHS U19 AG060917NIGMS NIH HHS U54 GM115516NIH HHS IH U19AG060917
6 · The paper itself

Abstract

Irisin is a myokine released from muscle during exercise with distinct signaling effects on tissues throughout the body, including an influence on skeletal remodeling. Our previous work has shown that irisin stimulates resorption, a key first step in bone remodeling, by enhancing osteoclastogenesis. The present study further investigates the action of irisin on the metabolic function of osteoclast progenitors during differentiation. Fluorescent imaging showed increased mitochondrial content and reactive oxygen species production with irisin treatment in osteoclast progenitors after 48 h of osteoclastogenic culture. Mitochondrial stress testing demonstrated a significant increase in maximal oxygen consumption rate and spare capacity after 48 h of preconditioning with irisin treatment. Together, these findings further elucidate the stimulatory action of irisin on osteoclastogenesis, demonstrating an enhancement of metabolism through mitochondrial respiration in the progenitor to support the energy demands of their differentiation into mature osteoclasts.

Indexed as

irisinmitochondriaosteoclastosteoclast progenitoroxidative respiration

Identifiers

PMID38137532
PMCPMC10741766
OpenAlexW4389816888

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.