Evidence map›Paper›PMID 39788511›Full record

ArticleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2024

Regulatory role of the mTOR signaling pathway in autophagy and mesangial proliferation in IgA nephropathy.

Yexin Liu, Bin Leng, Ming Xia, Di Liu, Xia Tan, Guochun Chen, Liyu He, Chang Wang, Xuejing Zhu, Hong Liu

Abstract read
In one paragraph

Article in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2024. 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

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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. 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

10 authors.

Yexin LiuDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011. 809072022@qq.com.
Bin LengDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011. 208202046@csu.edu.cn.
Ming XiaDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Di LiuDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Xia TanDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Guochun ChenDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Liyu HeDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Chang WangDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Xuejing ZhuDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011.
Hong LiuDepartment of Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011. liuhong618@csu.edu.cn.

Funding

the Key Funding Project of Hunan Provincial Health Commission A202303057091the Nephrology Medical Development Research Fund Project 20220316ZN
6 · The paper itself

Abstract

objectivesIgA nephropathy (IgAN) is the most common primary glomerular disease in China, but its pathogenesis remains unclear. This study aims to explore the regulatory role of the mammalian target of rapamycin (mTOR) signaling pathway in autophagy and mesangial proliferation during renal injury in IgA.

methodsThe activity of mTOR and autophagy was evaluated in kidney samples from IgAN patients and in an IgAN mouse model induced by oral bovine serum albumin and carbon tetrachloride (CCl4) injection. mTOR inhibitors (rapamycin) and activators [bpV(phen)] were administered to the IgAN mouse model to observe the effects of mTOR on autophagy and renal lesions. In human mesangial cells treated with polymeric IgA1 (p-IgA1) and mTOR modulators, the expression and distribution of cell cycle proteins were assessed, along with the effects of mTOR on mesangial cell proliferation and autophagy.

resultsIncreased mTOR activity and decreased autophagy were observed in kidney tissues from IgAN patients and the mouse model, as evidenced by elevated phosphorylated mTOR (p-mTOR) levels and reduced LC3 expression. In the IgAN mouse model, rapamycin inhibited mTOR, restored autophagy, reduced mesangial IgA deposition, alleviated mesangial cell proliferation, and decreased proteinuria (all

conclusionsInhibition of the mTOR signaling pathway enhances renal autophagy, reduces mesangial cell proliferation, and improves renal injury in IgAN.

Indexed as

AutophagyCell ProliferationGlomerulonephritis, IGAMesangial CellsSignal TransductionSirolimusTOR Serine-Threonine KinasesAnimalsDisease Models, AnimalHumansMaleMiceMTOR protein, humanmTOR protein, mouseSirolimusTOR Serine-Threonine KinasesautophagyIgA nephropathymammalian target of rapamycinmesangial proliferation

Identifiers

PMID39788511
PMCPMC11628233

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Registered trials

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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.