Evidence map›Paper›PMID 40369638›Full record

ArticleInflammation and regeneration2025

CD157

Ami Takii, Yukika Tanabe, Wenting Li, Hiroki Shiomi, Akane Inoue, Fumitaka Muramatsu, Weizhen Jia, Nobuyuki Takakura

Abstract read
In one paragraph

Article in Inflammation and regeneration, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

8 authors.

Ami TakiiDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Yukika TanabeDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Wenting LiDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Hiroki ShiomiDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Akane InoueDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Fumitaka MuramatsuDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Weizhen JiaDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan. jiawz@biken.osaka-u.ac.jp.
Nobuyuki TakakuraDepartment of Signal Transduction, Research Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan. ntakaku@biken.osaka-u.ac.jp.

Funding

Japan Agency for Medical Research and Development 24ama221533h0001Japan Agency for Medical Research and Development 24ck0106727h0003Japan Society for the Promotion of Science 20H05698Ministry of Education, Culture, Sports, Science and Technology JPMXP1323015484
6 · The paper itself

Abstract

backgroundWe previously reported that a vascular endothelial stem cell population resides in pre-existing blood vessels in mice and may contribute to vascular endothelial cells in liver injury or hind limb ischemia models in the long-term. However, whether such stem cells exist in humans and can differentiate specifically into vascular endothelial cells have not been determined. We hypothesized that CD157

methodsFirst, human-derived induced pluripotent stem cells were differentiated into vascular endothelial cells and the expression of CD157 was monitored during the differentiation process. We found that CD157 emerged 11 days after the induction of differentiation, peaked at 14 days, and then declined by 24 days. We also evaluated blood vessel formation by 14- and 24-day-old vascular endothelial cells.

resultsIt was found that 14-day-old cells, when CD157 expression was at its peak, formed more blood vessels than 24-day-old cells.

conclusionThese results suggest that vascular endothelial cells expressing CD157 have high angiogenic potential and may exist as vascular endothelial stem cells.

Indexed as

AngiogenesisCD157Endothelial cellsHuman iPSCStem cells

Identifiers

PMID40369638
PMCPMC12077006

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.