Evidence map›Paper›PMID 41607850›Full record

ArticleBiomedical reports2026

Starvation-induced NEDD4-mediated autophagy in BMSCs.

Chengyi Liu, Shuang Zhang, Xiaoxian Yun, Bo Li, Xiaomei Xu, Fuwei Lin

Abstract read
In one paragraph

Article in Biomedical reports, 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

6 authors.

Chengyi LiuLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Shuang ZhangLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Xiaoxian YunLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Bo LiLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Xiaomei XuLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Fuwei LinLuzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, The Affiliated Stomatological Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy regulates the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and mediates BMSC-mediated bone remodeling under pathological conditions (such as osteoporosis and infectious bone defects). However, the regulatory mechanisms controlling autophagy in BMSCs remain unclear. Neural precursor cell-expressed developmentally down-regulated protein 4 (NEDD4) has been implicated in autophagy regulation. In the present study, autophagy was induced in BMSCs through serum starvation and NEDD4 expression was silenced using lentiviral short hairpin RNA. Quantitative real-time polymerase chain reaction, western blotting, and immunofluorescence were used to examine the expression of the autophagy-related molecules, microtubule-associated protein 1 light chain 3 (LC3) and Beclin-1, to explore the underlying molecular mechanisms. It was determined that BMSCs exhibited significant autophagy activation 30 min after starvation, accompanied by marked increases in NEDD4, LC3, and Beclin-1 at both mRNA and protein levels. NEDD4 knockdown significantly attenuated the upregulation of LC3 and Beclin-1 and prevented the starvation-induced decrease in phosphorylated mTOR. These results indicated that NEDD4 positively regulates autophagy in BMSCs, likely through the mTOR signaling pathway. In conclusion, the present study demonstrated that NEDD4 is essential for BMSC autophagy and may serve as an important target for therapies aimed at modulating BMSC function.

Indexed as

autophagybone marrow mesenchymal stem cellsbone remodelingNEDD4serum starvation

Identifiers

PMID41607850
PMCPMC12836325

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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.