Evidence map›Paper›PMID 30987025›Full record

ArticleInternational journal of molecular sciences2019

Sphingosine-1-phosphate in Endothelial Cell Recellularization Improves Patency and Endothelialization of Decellularized Vascular Grafts In Vivo.

Kai Hsia, Chih-Hsun Lin, Hsin-Yu Lee, Wei-Min Chen, Chao-Ling Yao, Chien-Chin Chen, Hsu Ma, Shyh-Jen Wang, Jen-Her Lu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  5. Biofabrication of engineered blood vessels for biomedical applications.Science and technology of advanced materials · 2024
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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

9 authors at 5 institutions in 1 country.

Kai HsiaDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan. hkay1008@gmail.com.
Chih-Hsun LinDivision of Plastic Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan. chlin12@vghtpe.gov.tw.
Hsin-Yu LeeDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan. hsinyu@ntu.edu.tw.ORCID 0000-0002-1477-0183
Wei-Min ChenDepartment of Life Science, National Taiwan University, Taipei 10617, Taiwan. b99b01070@ntu.edu.tw.
Chao-Ling YaoDepartment of Chemical Engineering and Materials Science, Graduate School of Biotechnology and Bioengineering, Yuan Ze University, Chung-Li, Taoyuan City 32003, Taiwan. d897601@alumni.nthu.edu.tw.ORCID 0000-0002-7196-5833
Chien-Chin ChenDepartment of Pathology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi 600, Taiwan. hlmarkc@gmail.com.ORCID 0000-0001-9599-0884
Hsu MaDivision of Plastic Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan. sma@vghtpe.gov.tw.
Shyh-Jen WangDivision of Experimental Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan. wangsj@vghtpe.gov.tw.
Jen-Her LuDepartment of Pediatrics, Taipei Veterans General Hospital, Taipei 11217, Taiwan. jenherlu@gmail.com.ORCID 0000-0003-2056-3065
National Taiwan University · TWNational Yang Ming Chiao Tung University · TWChia-Yi Christian Hospital · TWTaipei Veterans General Hospital · TWYuan Ze University · TW

Funding

I-MEI FOODS CO., LTD &Taipei Veterans General Hospital R16001 & R16002
6 · The paper itself

Abstract

backgroundS1P has been shown to improve the endothelialization of decellularized vascular grafts in vitro. Here, we evaluated the potential of tissue-engineered vascular grafts (TEVGs) constructed by ECs and S1P on decellularized vascular scaffolds in a rat model.

methodsRat aorta was decellularized mainly by 0.1% SDS and characterized by histology. Rat ECs, were seeded onto decellularized scaffolds, and the viability of the ECs was evaluated by biochemical assays. Then, we investigated the in vivo patency rate and endothelialization for five groups of decellularized vascular grafts (each

resultsIn vitro, ECs were identified by the uptake of Dil-Ac-LDL. S1P enhanced the expression of syndecan-1 on ECs and supported the proliferation of ECs on decellularized vascular grafts. In vivo, RAA and DRAA/EC/S1P both had 100% patency without thrombus formation within 14 days. Better endothelialization, more wall structure maintenance and less inflammation were noted in the DRAA/EC/S1P group. In contrast, there was thrombus formation in the DRAA, DRAA/S1P and DRAA/EC groups.

conclusionS1P could inhibit thrombus formation to improve the patency rate of EC-covered decellularized vascular grafts in vivo and may play an important role in the construction of TEVGs.

Indexed as

Blood Vessel ProsthesisVascular PatencyAnimalsAortaBlood Vessel Prosthesis ImplantationCell ProliferationCell ShapeEndothelial CellsFemaleLysophospholipidsMacrophagesRats, Sprague-DawleySphingosineSurvival AnalysisSyndecan-1LysophospholipidsSphingosinesphingosine 1-phosphateSyndecan-1endothelial cellsphingosine-1-phosphatesyndecan-1thrombosisvascular graft

Identifiers

PMID30987025
PMCPMC6480112
OpenAlexW2932974834

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.