Evidence map›Paper›PMID 41068421›Full record

ArticleNature metabolism2025

Early-life ketone body signalling promotes beige fat biogenesis through changes in histone acetylome and β-hydroxybutyrylome.

Chung-Lin Jiang, Pei-Hsiang Lai, Po-Cheng Yang, Chia-Jung Lien, Hsueh-Ping Catherine Chu, Jian-Da Lin, Sung-Jan Lin, I-Shing Yu, Fu-Jung Lin

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Article in Nature metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Chung-Lin JiangDepartment of Biochemical Science and Technology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0001-8293-2984
Pei-Hsiang LaiDepartment of Biochemical Science and Technology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0009-0007-3165-3038
Po-Cheng YangInstitute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0009-0002-7247-4558
Chia-Jung LienDepartment of Biochemical Science and Technology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0009-0008-1783-2723
Hsueh-Ping Catherine ChuInstitute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-0281-0942
Jian-Da LinDepartment of Biochemical Science and Technology, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-3697-4766
Sung-Jan LinDepartment of Biomedical Engineering, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-1325-3464
I-Shing YuLaboratory Animal Center, College of Medicine, National Taiwan University, Taipei, Taiwan.
Fu-Jung LinDepartment of Biochemical Science and Technology, National Taiwan University, Taipei, Taiwan. fujlin@ntu.edu.tw.ORCID http://orcid.org/0000-0003-4065-0983

Funding

National Taiwan University (NTU) 112L7131National Taiwan University (NTU) 113L894803National Taiwan University (NTU) 114L893003
6 · The paper itself

Abstract

Infants undergo distinct ketogenesis during the preweaning period, yet its physiological implications remain unclear. Here, we show that preweaning ketosis promotes beige fat biogenesis and improves health outcomes in adulthood. Loss of ketogenesis in neonatal mice by early weaning or ablation of Hmgcs2 hinders beige adipogenesis, subsequently exacerbating metabolic dysregulation in high-fat diet-induced obesity. Enhanced ketogenesis during lactation through exogenous ketone supplements enhances energy expenditure, beige fat formation, and mitochondrial biogenesis and respiration. Using single-cell RNA sequencing, we identified a subset of β-hydroxybutyrate-responsive adipocyte progenitor cells (APCs) expressing Cd81 that showed high beige adipogenic potential. Enhanced ketogenesis promotes the recruitment of beige APCs and their differentiation into beige adipocytes. Mechanistically, ketogenesis-derived βHB induces a switch in the histone acetylome and β-hydroxybutyrylome for transcriptional activation of beige fat biogenesis genes. Notably, enhanced ketogenesis during lactation alleviates adverse metabolic effects predisposed by parental obesity. Our study highlights that targeting preweaning ketosis to drive beige adipogenesis may offer a therapeutic approach to combat obesity and metabolic diseases in adulthood.

Indexed as

3-Hydroxybutyric AcidAdipose Tissue, BeigeHistonesKetone BodiesAcetylationAdipocytes, BeigeAdipogenesisAnimalsAnimals, NewbornDiet, High-FatEnergy MetabolismFemaleMaleMiceMice, Inbred C57BLObesity3-Hydroxybutyric AcidHistonesKetone Bodies

Identifiers

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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.