Evidence map›Paper›PMID 40721814›Full record

ArticleStem cell research & therapy2025

SMAD3 and HIF-1α orchestrate metabolic transition to aerobic glycolysis as a critical prerequisite for spontaneous reprogramming of spermatogonial stem cells.

Yihui Cai, Jian Wen, Hongyang Liu, Rui Wei, Xiaoxiao Li, Yao Dong, Keren Cheng, Kang Zou

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Yihui Cai *Germline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Jian Wen *Germline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Hongyang Liu *Germline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Rui WeiGermline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Xiaoxiao LiGermline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Yao DongGermline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Keren ChengDepartment of Obstetrics and Gynecology, Center for Reproductive Medicine, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Kang ZouGermline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China. kangzou@njau.edu.cn.ORCID http://orcid.org/0000-0002-1253-1816

Funding

National Key Research & Development Program of China 2022YFD1302200National Key Research & Development Program of China 2024YFA1108100
6 · The paper itself

Abstract

Spermatogonial stem cells (SSCs) possess the capacity for spontaneous reprogramming during in vitro culture, while the underlying mechanisms remain poorly understood, especially why the addition of epidermal growth factor (EGF), leukemia inhibitory factor (LIF) remarkably enhanced transition efficiency. Here we employed a multi-omics approach, integrating transcriptomics, metabolomics, and DNA methylation analyses to focus on the interplay between exogenous growth factors, metabolic pathways, and signaling cascades, particularly the role of SMAD3 in these networks. Our findings reveal that SSC reprogramming is contingent upon a metabolic shift from the tricarboxylic acid (TCA) cycle to aerobic glycolysis, modulated by fluctuating SMAD3 levels. SMAD3 downregulation activates HIF-1α, inducing aerobic glycolysis to supply energy and substrates for reprogramming. Subsequent SMAD3 reactivation promotes rapid cell proliferation, facilitating successful reprogramming. This study elucidates the pivotal role of SMAD3 in modulating glycometabolic pathways driving SSC transformation, emphasizing the necessity of aerobic glycolysis following SMAD3 fluctuations for effective reprogramming, which provides novel insights into the intricate interplay between energy metabolism and stem cell plasticity and potential applications in regenerative medicine and fertility treatments.

Indexed as

Cellular ReprogrammingGlycolysisHypoxia-Inducible Factor 1, alpha SubunitSmad3 ProteinSpermatogoniaAnimalsCell ProliferationCitric Acid CycleMaleMiceHypoxia-Inducible Factor 1, alpha SubunitSmad3 ProteinSmad3 protein, mouseAerobic glycolysisCell fateCellular plasticityGermline-to-pluripotent transitionHIF-1A activationMetabolic reprogrammingSMAD3 signaling

Identifiers

PMID40721814
PMCPMC12305914

What Socratic 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 Socratic graph.