Evidence map›Paper›PMID 40050412›Full record

ArticleNature aging2025

Mitochondria-enriched hematopoietic stem cells exhibit elevated self-renewal capabilities, thriving within the context of aged bone marrow.

Haruhito Totani, Takayoshi Matsumura, Rui Yokomori, Terumasa Umemoto, Yuji Takihara, Chong Yang, Lee Hui Chua, Atsushi Watanabe, Takaomi Sanda, Toshio Suda

Abstract read
PubMed Publisher
In one paragraph

Article in Nature aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

10 authors.

Haruhito Totani *Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0001-8395-8975
Takayoshi Matsumura *Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore. matsut@jichi.ac.jp.ORCID http://orcid.org/0000-0003-3394-9506
Rui YokomoriCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Terumasa UmemotoInternational Research Center of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID http://orcid.org/0000-0003-0423-9003
Yuji TakiharaCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0002-0374-4174
Chong YangCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Lee Hui ChuaCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0002-7564-659X
Atsushi WatanabeCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Takaomi SandaCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0003-1621-4954
Toshio SudaCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore. sudato@keio.jp.ORCID http://orcid.org/0000-0001-7540-1771

Funding

Chinese Academy of Medical Sciences (CAMS) 2024-12M-3-017MEXT | Japan Society for the Promotion of Science (JSPS) 18H05284MEXT | Japan Society for the Promotion of Science (JSPS) 24K11298MEXT | Japan Society for the Promotion of Science (JSPS) 26221309MEXT | Japan Society for the Promotion of Science (JSPS) JP21K19514MOH | National Medical Research Council (NMRC) NMRC/STaR 18 may-0004MOH | National Medical Research Council (NMRC) OFYIRG21nov-0020National Natural Science Foundation of China (National Science Foundation of China) W2441024
6 · The paper itself

Abstract

The aging of hematopoietic stem cells (HSCs) substantially alters their characteristics. Mitochondria, essential for cellular metabolism, play a crucial role, and their dysfunction is a hallmark of aging-induced changes. The impact of mitochondrial mass on aged HSCs remains incompletely understood. Here we demonstrate that HSCs with high mitochondrial mass during aging are not merely cells that have accumulated damaged mitochondria and become exhausted. In addition, these HSCs retain a high regenerative capacity and remain in the aging bone marrow. Furthermore, we identified GPR183 as a distinct marker characterizing aged HSCs through single-cell analysis. HSCs marked by GPR183 were also enriched in aged HSCs with high mitochondrial mass, possessing a high capacity of self-renewal. These insights deepen understanding of HSC aging and provide additional perspectives on the assessment of aged HSCs, underscoring the importance of mitochondrial dynamics in aging.

Indexed as

AgingCell Self RenewalHematopoietic Stem CellsMitochondriaReceptors, G-Protein-CoupledAnimalsBone MarrowFemaleMaleMiceMice, Inbred C57BLSingle-Cell AnalysisGpr183 protein, mouseReceptors, G-Protein-Coupled

Identifiers

PMID40050412

What Socratic 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 Socratic graph.