Evidence map›Paper›PMID 39354086›Full record

ArticleScientific reports2024

Angiogenic properties and intercellular communication of differentiated porcine endothelial cells in vascular therapy.

Bo-Gyeong Seo, In-Won Lee, Hyo-Jin Kim, Yeon-Ji Lee, Okhwa Kim, Joon-Hee Lee, Jeong-Hyung Lee, Cheol Hwangbo

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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

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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

8 authors.

Bo-Gyeong Seo *Division of Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea.
In-Won Lee *Division of Applied Life Science (BK21 Four), Research Institute of Life Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea.
Hyo-Jin KimDivision of Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea.
Yeon-Ji LeeDivision of Applied Life Science (BK21 Four), Research Institute of Life Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea.
Okhwa KimKangwon Institute of Inclusive Technology, Kangwon National University, Chuncheon, Gangwon-do, 24341, Republic of Korea.
Joon-Hee LeeDepartment of Animal Bioscience, College of Agriculture & Life Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea. sbxjhl@gnu.ac.kr.
Jeong-Hyung LeeKangwon Institute of Inclusive Technology, Kangwon National University, Chuncheon, Gangwon-do, 24341, Republic of Korea. jhlee36@kangwon.ac.kr.
Cheol HwangboDivision of Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, 52828, Republic of Korea. chwangbo@gnu.ac.kr.

Funding

National Research Foundation of Korea NRF-2021R1C1C1006516Technology Innovation Program, Korea 20022828
6 · The paper itself

Abstract

Endothelial cell dysfunction can lead to various vascular diseases. Blood flow disorder is a common symptom of vascular diseases. Regenerative angiogenesis, which involves transplanting vascular cells or stem cells into the body to shape new vasculature, can be a good therapeutic strategy. However, there are several limitations to using autologous cells from the patients themselves. We sought to investigate the new vascular cells that can play a role in the formation of angiogenesis in vivo using stem cells from alternative animals suitable for cellular therapy. Porcine is an optimal animal model for xenotransplantation owing to its physiological similarity to humans. We used differentiated porcine endothelial cells (pECs) as a therapeutic strategy to restore vessel function. Differentiated pECs formed vessel-like structures in mice, distinguishing them from stem cells. MMPs activity and migration assays indicated that differentiated pECs possessed angiogenic potential. Tube formation and 3D spheroid sprouting assays further confirmed the angiogenic phenotype of the differentiated pECs. Immunofluorescence and immunoprecipitation analyses revealed claudin-mediated tight junctions and connexin 43-mediated gap junctions between human ECs and differentiated pECs. Additionally, the movement of small RNA from human ECs to differentiated pECs was observed under co-culture conditions. Our findings demonstrated the in vivo viability and angiogenetic potential of differentiated pECs and highlighted the potential for intercellular communication between human and porcine ECs. These results suggest that transplanted cells in vascular regeneration completed after cell therapy have the potential to achieve intercellular communication within the body.

Indexed as

Cell CommunicationCell DifferentiationEndothelial CellsNeovascularization, PhysiologicAnimalsCells, CulturedCoculture TechniquesGap JunctionsHumansMiceSwineAngiogenesisCellular therapyEndothelial cellsPorcineXenotransplantation

Identifiers

PMID39354086
PMCPMC11445381

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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.