Evidence map›Paper›PMID 26858818›Full record

ArticleBiomicrofluidics2016

Human induced pluripotent stem cells derived endothelial cells mimicking vascular inflammatory response under flow.

Li Wang, Meng Xiang, Yingying Liu, Ning Sun, Meng Lu, Yang Shi, Xinhong Wang, Dan Meng, Sifeng Chen, Jianhua Qin

Abstract read
In one paragraph

Article in Biomicrofluidics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  10. Sourcing cells forFrontiers in medical technology · 2022
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  15. Article
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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.

Li Wang
Meng XiangDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Yingying LiuDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Ning SunDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Meng LuDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Yang ShiDalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023, People's Republic of China.
Xinhong WangDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Dan MengDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Sifeng ChenDepartment of Physiology and Pathophysiology, College of Basic Medical Sciences, Fudan University , Shanghai 200032, People's Republic of China.
Jianhua QinDalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cells (ECs) have great potential in vascular diseases research and regenerative medicine. Autologous human ECs are difficult to acquire in sufficient numbers in vitro, and human induced pluripotent stem cells (iPSCs) offer unique opportunity to generate ECs for these purposes. In this work, we present a new and efficient method to simply differentiate human iPSCs into functional ECs, which can respond to physiological level of flow and inflammatory stimulation on a fabricated microdevice. The endothelial-like cells were differentiated from human iPSCs within only one week, according to the inducing development principle. The expression of endothelial progenitor and endothelial marker genes (GATA2, RUNX1, CD34, and CD31) increased on the second and fourth days after the initial inducing process. The differentiated ECs exhibited strong expression of cells-specific markers (CD31 and von Willebrand factor antibody), similar to that present in human umbilical vein endothelial cells. In addition, the hiPSC derived ECs were able to form tubular structure and respond to vascular-like flow generated on a microdevice. Furthermore, the human induced pluripotent stem cell-endothelial cells (hiPSC-ECs) pretreated with tumor necrosis factor (TNF-α) were susceptible to adhesion to human monocyte line U937 under flow condition, indicating the feasibility of this hiPSCs derived microsystem for mimicking the inflammatory response of endothelial cells under physiological and pathological process.

Identifiers

PMID26858818
PMCPMC4714980

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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.