Evidence map›Paper›PMID 28247865›Full record

ArticleCellular and molecular gastroenterology and hepatology2015

Perivascular Interstitial Cells of Cajal in Human Colon.

Yuan-An Liu, Yuan-Chiang Chung, Ming-Yin Shen, Shien-Tung Pan, Chun-Wei Kuo, Shih-Jung Peng, Pankaj J Pasricha, Shiue-Cheng Tang

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Yuan-An LiuConnectomics Research Center, National Tsing Hua University, Hsinchu, Taiwan.
Yuan-Chiang ChungDepartment of Surgery, Cheng Ching General Hospital, Chung Kang Branch, Taichung, Taiwan.
Ming-Yin ShenDivision of Colorectal Surgery, National Taiwan University Hospital, Hsinchu Branch, Hsinchu, Taiwan.
Shien-Tung PanDepartment of Pathology, Miaoli General Hospital, Miaoli, Taiwan.
Chun-Wei KuoDepartment of Pathology, National Taiwan University Hospital, Hsinchu Branch, Hsinchu, Taiwan.
Shih-Jung PengConnectomics Research Center, National Tsing Hua University, Hsinchu, Taiwan; Department of Medical Science, National Tsing Hua University, Hsinchu, Taiwan.
Pankaj J PasrichaDivision of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Shiue-Cheng TangConnectomics Research Center, National Tsing Hua University, Hsinchu, Taiwan; Department of Medical Science, National Tsing Hua University, Hsinchu, Taiwan.
National Tsing Hua University · TWNational Taiwan University Hospital · TWCheng Ching Hospital · TWJohns Hopkins Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsInterstitial cells of Cajal (ICC) closely associate with nerves and smooth muscles to modulate gut motility. In the ICC microenvironment, although the circulating hormones/factors have been shown to influence ICC activities, the association between ICC and microvessels in the gut wall has not been described. We applied three-dimensional (3D) vascular histology with c-kit staining to identify the perivascular ICC and characterize their morphologic and population features in the human colon wall.

methodsFull-thickness colons were obtained from colectomies performed for colorectal cancer. We targeted the colon wall away from the tumor site. Confocal microscopy with optical clearing (use of immersion solution to reduce scattering in optical imaging) was performed to simultaneously reveal the ICC and vascular networks in space. 3D image rendering and projection were digitally conducted to illustrate the ICC-vessel contact patterns.

resultsPerivascular ICC were identified in the submucosal border, myenteric plexus, and circular and longitudinal muscles via high-definition 3D microscopy. Through in-depth image projection, we specified two contact patterns-the intimate cell body-to-vessel contact (type I, 18% of ICC in circular muscle) and the long-distance process-to-vessel contact (type II, 16%)-to classify perivascular ICC. Particularly, type I perivascular ICC were detected with elevated c-kit staining levels and were routinely found in clusters, making them readily distinguishable from other ICC in the network.

conclusionsWe propose a new subclass of ICC that closely associates with microvessels in the human colon. Our finding suggests a functional relationship between these mural ICC and microvessels based on the morphologic proximity.

Indexed as

3D Histology3D, three-dimensional5-HT, serotoninc-kitICCICC-CM, ICC in the circular muscleICC, interstitial cells of CajalICC-LM, ICC in the longitudinal muscleICC-MY, ICC around the myenteric plexusICC-SM, ICC at the submucosal borderMural CellsNA, numerical aperturePBS, phosphate-buffered salineSCF, stem cell factor

Identifiers

PMID28247865
PMCPMC5301165
OpenAlexW2049957312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.