Evidence map›Paper›PMID 38354087›Full record

ArticleCell reports2024

Proline restores mitochondrial function and reverses aging hallmarks in senescent cells.

Debanik Choudhury, Na Rong, Hamsa Vardini Senthil Kumar, Sydney Swedick, Ronel Z Samuel, Pihu Mehrotra, John Toftegaard, Nika Rajabian, Ramkumar Thiyagarajan, Ashis K Podder and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
14.7field-weighted citation impact, top 1% 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

39 citing papers in PubMed, 38 citations in OpenAlex.

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  15. Mitochondrial regulation of cellular senescence heterogeneity.Frontiers in cell and developmental biology · 2026
    Review
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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

16 authors at 1 institution in 1 country.

Debanik ChoudhuryDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Na RongDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Hamsa Vardini Senthil KumarDepartment of Genetics, Genomics and Bioinformatics, University at Buffalo, Buffalo, NY 14263, USA.
Sydney SwedickDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Ronel Z SamuelDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Pihu MehrotraDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
John ToftegaardDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Nika RajabianDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Ramkumar ThiyagarajanDepartment of Medicine, Division of Geriatrics and Palliative Medicine, Buffalo, NY 14203, USA.
Ashis K PodderDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Yulun WuDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Shahryar ShahiniDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Kenneth L SeldeenDepartment of Medicine, Division of Geriatrics and Palliative Medicine, Buffalo, NY 14203, USA.
Bruce TroenDepartment of Medicine, Division of Geriatrics and Palliative Medicine, Buffalo, NY 14203, USA.
Pedro LeiDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Stelios T AndreadisDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY 14260, USA; Department of Biomedical Engineering, University at Buffalo, Buffalo, NY 14260, USA; Center of Excellence in Bioinformatics and Life Sciences, University at Buffalo, Buffalo, NY 14263, USA; Center for Cell, Gene and Tissue Engineering (CGTE), University at Buffalo, Buffalo, NY 14260, USA. Electronic address: sandread@buffalo.edu.
University at Buffalo, State University of New York · US

Funding

Restoring the regenerative capacity of the aged muscleR01AG068250 · NIA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2020 to 2024
$2.0M
High throughput genetic and functional screens for restoring stem cell potentialR01AG052387 · NIA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2017 to 2019
$1.2M
Enhancing Geroscience Scholarship and Faculty Development to Minimize Frailty and Maximize HealthspanK07AG060266 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI TROEN, BRUCE R. · 2019 to 2023
$774k
High intensity interval training and nicotinamide riboside treatment to enhance functional capacity and reduce frailty during agingI01BX004369 · VA · VA WESTERN NEW YORK HEALTHCARE SYSTEM · PI TROEN, BRUCE R. · 2019 to 2023
–
BLRD VA I01 BX004369NIA NIH HHS K07 AG060266NIA NIH HHS R01 AG052387NIA NIH HHS R01 AG068250
6 · The paper itself

Abstract

Mitochondrial dysfunction is a hallmark of cellular senescence, with the loss of mitochondrial function identified as a potential causal factor contributing to senescence-associated decline in cellular functions. Our recent findings revealed that ectopic expression of the pluripotency transcription factor NANOG rejuvenates dysfunctional mitochondria of senescent cells by rewiring metabolic pathways. In this study, we report that NANOG restores the expression of key enzymes, PYCR1 and PYCR2, in the proline biosynthesis pathway. Additionally, senescent mesenchymal stem cells manifest severe mitochondrial respiratory impairment, which is alleviated through proline supplementation. Proline induces mitophagy by activating AMP-activated protein kinase α and upregulating Parkin expression, enhancing mitochondrial clearance and ultimately restoring cell metabolism. Notably, proline treatment also mitigates several aging hallmarks, including DNA damage, senescence-associated β-galactosidase, inflammatory cytokine expressions, and impaired myogenic differentiation capacity. Overall, this study highlights the role of proline in mitophagy and its potential in reversing senescence-associated mitochondrial dysfunction and aging hallmarks.

Indexed as

MitochondriaMitochondrial DiseasesCellular SenescenceHumansProlineProlineagingamino acidAMPKαautophagyCP: Cell biologyCP: MetabolismmitochondriamitophagyParkinprolinesenescence

Identifiers

PMID38354087
PMCPMC13092368
OpenAlexW4391740614

What Socratic holds

Textmetadata
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 Socratic graph.