Evidence map›Paper›PMID 41965337›Full record

ArticleNature communications2026

Adipocytes signal to recruit specific mRNAs from surrounding cells to restore expression deficits.

Clair Crewe, Christy M Gliniak, Toshiharu Onodera, Shiuhwei Chen, Jan-Bernd Funcke, May-Yun Wang, Snigdha Tiash, Yun-Ling Pai, Marjori Russo, Saket Awadhesbhai Patel and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Clair CreweDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA. clair.crewe@wustl.edu.ORCID http://orcid.org/0000-0002-3117-5327
Christy M GliniakTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Toshiharu OnoderaTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-4439-0077
Shiuhwei ChenTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Jan-Bernd FunckeTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-2596-3167
May-Yun WangTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Snigdha TiashDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Yun-Ling PaiDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Marjori RussoDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Saket Awadhesbhai PatelDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Ze YuMcDermott Center of Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-0583-1351
Yi-Cian ZhengDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Alex LarkinDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Chao XingMcDermott Center of Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-1838-0502
Laurent GautronCenter for Hypothalamic Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-3609-7441
Chun-Kan ChenDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Chen LiuCenter for Hypothalamic Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-5922-0951
Philipp E SchererTouchstone Diabetes Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-0680-3392

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Hypothalamic Serotonin Receptors and Olanzapine-induced Metabolic SyndromeR01DK114036 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Chen Liu · 2017 to 2026
$4.2M
Transcriptional Control of Melanocortin 4 Receptors and Obesity RiskR01DK130892 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Chen Liu · 2022 to 2026
$2.4M
Deconstruct Raphe Serotonin Neurons that Regulate SatietyR01DK136592 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Chen Liu · 2024 to 2026
$1.5M
Endothelial cell-assisted extracellular vesicle bioengineering for cytoplasmic delivery of therapeutic moleculesR21EB035738 · NIBIB · WASHINGTON UNIVERSITY · PI CREWE, CLAIR · 2024 to 2024
$622k
American Heart Association (American Heart Association, Inc.) 23IPA1054013NIBIB NIH HHS R21 EB035738NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK056341NIDDK NIH HHS R01 DK114036NIDDK NIH HHS R01 DK130892NIDDK NIH HHS R01 DK136592U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R21EB035738U.S. Department of Health & Human Services | National Institutes of Health (NIH) P01-AG051459U.S. Department of Health & Human Services | National Institutes of Health (NIH) P30DK020579U.S. Department of Health & Human Services | National Institutes of Health (NIH) R00-DK122019U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-DK099110U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01- DK114036U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-DK127274U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01- DK130892U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-DK131537U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-DK143576U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-DK55758
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are nano-sized, membrane-delimited, particles released by cells that carry signaling macromolecules. A major pathway of EV production is potentiated by neutral sphingomyelinase 2 (SMPD3/nSMAse2), an enzyme that generates ceramide from sphingomyelin. In our attempt to study this pathway in adipocytes of male mice, we discover that the elimination of SMPD3 from adipocytes in vivo triggers a signal to surrounding immune cell-like preadipocytes to release EVs that carry SMPD3 mRNA. This results in a widespread increase in SMPD3 mRNA in purified null adipocytes without a change in the transcripts of other enzymes involved in ceramide metabolism. These results point to a selective mechanism by which specific mRNA molecules are acquired from the microenvironment to a level that can restore expression of mRNA and protein in a cell that is depleted of the corresponding genetic information.

Indexed as

AdipocytesRNA, MessengerSphingomyelin PhosphodiesteraseAnimalsCeramidesMaleMiceMice, KnockoutSignal TransductionCeramidesRNA, MessengerSmpd3 protein, mouseSphingomyelin Phosphodiesterase

Identifiers

PMID41965337
PMCPMC13247252

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.