Evidence map›Paper›PMID 36451096›Full record

ArticleBasic and clinical andrology2022

Improvement of erectile dysfunction using endothelial progenitor cells from fetal cerebral vasculature in the cavernous nerve injury of rats.

Jae Heon Kim, Sang Hong Bak, Hee Jo Yang, Seung Whan Doo, Do Kyung Kim, Won Jae Yang, Seung U Kim, Hong J Lee, Yun Seob Song

Open access · goldAbstract read
In one paragraph

Article in Basic and clinical andrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 3 institutions in 3 countries.

Jae Heon Kim *Department of Urology, Soonchunhyang University School of Medicine, 04401, Seoul, Republic of Korea.
Sang Hong Bak *Research Institute, e-Biogen Inc., Seoul, Republic of Korea.
Hee Jo Yang *Department of Urology, Soonchunhyang University School of Medicine, Cheonan, Republic of Korea.
Seung Whan DooDepartment of Urology, Soonchunhyang University School of Medicine, 04401, Seoul, Republic of Korea.
Do Kyung KimDepartment of Urology, Soonchunhyang University School of Medicine, 04401, Seoul, Republic of Korea.
Won Jae YangDepartment of Urology, Soonchunhyang University School of Medicine, 04401, Seoul, Republic of Korea.
Seung U KimDivision of Neurology, Department of Medicine, UBC Hospital, University of British Columbia, Vancouver, Canada.
Hong J LeeResearch Institute, e-Biogen Inc., Seoul, Republic of Korea. leehj71@gmail.com.ORCID http://orcid.org/0000-0003-2641-6437
Yun Seob SongDepartment of Urology, Soonchunhyang University School of Medicine, 04401, Seoul, Republic of Korea. schurology1@gmail.com.ORCID http://orcid.org/0000-0002-0909-3341
Soonchunhyang University · KRBiogen (United States) · USUniversity of British Columbia Hospital · CA

Funding

Ministry of Education, Science and Technology 2021R1A2C1004163
6 · The paper itself

Abstract

backgroundBecause of limited differentiation to endothelium from mesenchymal stem cells, it has been strongly recommended to use endothelial progenitor cells for the regeneration of the damaged endothelium of corpora cavernosa. This study was performed to investigate the immortalized human cerebral endothelial cells and their capability for repairing erectile dysfunction in a rat model of cavernous nerve injury. Circulating endothelial progenitor cells were isolated from human fetal brain vasculature at the periventricular region of telencephalic tissues. Over 95% of CD 31-positive cells were sorted and cultured for 10 days. Human cerebral endothelial progenitor cells were injected into the cavernosa of rats with cavernous nerve injury. Erectile response was then assessed. In in vivo assays, rats were divided into three groups: group 1, sham operation: group 2, bilateral cavernous nerve injury: and group 3, treatment with human cerebral endothelial cells after cavernous nerve injury.

resultsEstablished immortalized circulating endothelial progenitor cells showed expression of human telomerase reverse transcriptase transcript by RT-PCR. They also showed the expression of vascular endothelial growth factor, von Willebrand factor, vascular endothelial growth factor receptor, and CD31, cell type-specific markers for endothelial cells by RT-PCR. In in vitro angiogenesis assays, they demonstrated tube formation that suggested morphological properties of endothelial progenitor cells. In in vivo assays, impaired erectile function of rat with cavernous nerve injury recovered at 2, 4, and 12 weeks after transplantation of human cerebral endothelial cells into the cavernosa.

conclusionsTelomerase reverse transcriptase-circulating endothelial progenitor cells from fetal brain vasculature could repair erectile dysfunction of rats with cavernous nerve injury.

Indexed as

Erectile dysfunctionHuman endothelial cellsHuman telomerase reverse transcriptase

Identifiers

PMID36451096
PMCPMC9714194
OpenAlexW4310641809

What OpenQuestion holds

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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.