Evidence map›Paper›PMID 30920150›Full record

ArticleJournal of cellular and molecular medicine2019

Vascular progenitor cell senescence in patients with Marfan syndrome.

Haiwei He, Baoqi Yu, Zipeng Liu, Gen Ye, Wei You, Yimei Hong, Qizhou Lian, Yuelin Zhang, Xin Li

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Molecular Genetics of Marfan Syndrome.International journal of medical sciences · 2021
    Review
  9. Article
  10. Review
  11. Vascular progenitor cell senescence in patients with Marfan syndrome.Journal of cellular and molecular medicine · 2019
    Article
  12. Article
  13. 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

9 authors at 4 institutions in 3 countries.

Haiwei HeSchool of Medicine, South China University of Technology, Guangzhou, China.
Baoqi YuDepartment of Emergency Medicine, Department of Emergency and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Zipeng LiuCenter for Genomic Sciences, LKS Faculty of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Gen YeDepartment of Emergency Medicine, Department of Emergency and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Wei YouDepartment of Emergency Medicine, Department of Emergency and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Yimei HongSchool of Medicine, South China University of Technology, Guangzhou, China.
Qizhou LianDepartment of Medicine, LKS Faculty of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Yuelin ZhangDepartment of Emergency Medicine, Department of Emergency and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Xin LiSchool of Medicine, South China University of Technology, Guangzhou, China.ORCID 0000-0003-0469-5121
Guangdong Academy of Medical Sciences · CNCapital Medical University · CNCenter for Genomic Science · ITChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular progenitor cells (VPCs) present in the adventitia of the vessel wall play a critical role in the regulation of vascular repair following injury. This study aimed to assess the function of VPCs isolated from patients with Marfan syndrome (MFS). VPCs were isolated from control and MFS donors and characterized. Compared with control-VPCs, MFS-VPCs exhibited cellular senescence as demonstrated by increased cell size, higher SA-β-gal activity and elevated levels of p53 and p21. RNA sequencing showed that several cellular process-related pathways including cell cycle and cellular senescence were significantly enriched in MFP-VPCs. Notably, the expression level of TGF-β1 was much higher in MFS-VPCs than control-VPCs. Treatment of control-VPCs with TGF-β1 significantly enhanced mitochondrial reactive oxidative species (ROS) and induced cellular senescence whereas inhibition of ROS reversed these effects. MFS-VPCs displayed increased mitochondrial fusion and decreased mitochondrial fission. Treatment of control-VPCs with TGF-β1 increased mitochondrial fusion and reduced mitochondrial fission. Nonetheless, treatment of mitofusin2 (Mfn2)-siRNA inhibited TGF-β1-induced mitochondrial fusion and cellular senescence. Furthermore, TGF-β1-induced mitochondrial fusion was mediated by the AMPK signalling pathway. Our study shows that TGF-β1 induces VPC senescence in patients with MFS by mediating mitochondrial dynamics via the AMPK signalling pathway.

Indexed as

AdultCellular SenescenceFemaleHumansMaleMarfan SyndromeMitochondriaMitochondrial DynamicsReactive Oxygen SpeciesSignal TransductionStem CellsTransforming Growth Factor beta1Reactive Oxygen SpeciesTransforming Growth Factor beta1Marfan syndromemitochondria dynamicssenescencetransforming growth factor βvascular progenitor cells

Identifiers

PMID30920150
PMCPMC6533473
OpenAlexW2928733249

What OpenQuestion 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 OpenQuestion graph.