Evidence map›Paper›PMID 31760535›Full record

ArticleCellular and molecular neurobiology2020

Increased Fibronectin Impairs the Function of Excitatory/Inhibitory Synapses in Hirschsprung Disease.

Ni Gao, Peimin Hou, Jian Wang, Tingting Zhou, Dongming Wang, Qiangye Zhang, Weijing Mu, Xiaona Lv, Aiwu Li

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
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  5. 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 1 institution in 1 country.

Ni GaoDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Peimin HouDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Jian WangDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Tingting ZhouDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Dongming WangDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Qiangye ZhangDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Weijing MuDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Xiaona LvDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China. 502661480@qq.com.
Aiwu LiDepartment of Pediatric Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China. aiwulips@126.com.
Qilu Hospital of Shandong University · CN

Funding

National Natural Science Foundation of China 81270720National Natural Science Foundation of China 81471487National Natural Science Foundation of China 81701492
6 · The paper itself

Abstract

Although approximately 50% of cases have a known genetic defect, the precise pathogenesis of Hirschsprung disease (HSCR) is still unclear. We recently reported that expression of fibronectin (FN), which is involved in the migration, colonization, and differentiation of enteric neural crest cells (ENCCs), is increased in aganglionic colonic segments obtained from patients. We hypothesized that abnormally high levels of FN might play a role in the etiology of HSCR. Here, to test this hypothesis, we investigated aganglionic, transitional, and ganglionic colon segments from 63 children with HSCR and distal colon from thirty healthy Wistar rats at embryonic day 20, in addition to in vitro studies with PC12 Adh neural crest cells. We measured the protein and mRNA expression levels of FN, together with a panel of excitatory (VGLUT1, GluA1, GluN1, PSD-95, and NL-1) and inhibitory (GAD67, GABA AR-α1, NL-2, and SLC32) synaptic markers. Expression of all these synaptic markers was significantly decreased in aganglionic colon, compared to ganglionic colon, whereas expression of FN was significantly increased. In a neural crest cell line, PC12 Adh, knockdown of FN with small-interfering RNA increased the expression of synaptic markers. Co-culture of colons from embryonic day 20 rats with RGD recombinant protein, which contains the RGD motif of FN, reduced the expression of excitatory and inhibitory synaptic markers. These results are consistent with the idea that the etiology of HSCR involves aberrant overexpression of FN, which may impair synaptic function and enteric nervous system development, leading to motor dysfunction of intestinal muscles.

Indexed as

Neural InhibitionAnimalsBiomarkersChildChild, PreschoolColonFemaleFibronectinsHirschsprung DiseaseHumansInfantInfant, NewbornMaleMyenteric PlexusPC12 CellsRatsBiomarkersFibronectinsEnteric neural crest cellsFibronectinHirschsprung diseaseSynaptic functions

Identifiers

PMID31760535
PMCPMC11448818
OpenAlexW2990505307

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.