Evidence map›Paper›PMID 36382711›Full record

ArticleThe EMBO journal2023

Fecal microbiota transplantation enhances cell therapy in a rat model of hypoganglionosis by SCFA-induced MEK1/2 signaling pathway.

Donghao Tian, Wenyao Xu, Weikang Pan, Baijun Zheng, Weili Yang, Wanying Jia, Yong Liu, Malgorzata A Garstka, Ya Gao, Hui Yu

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 29 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

10 authors at 2 institutions in 1 country.

Donghao Tian *Department of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-1886-6123
Wenyao Xu *Department of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Weikang PanDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Baijun ZhengDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Weili YangDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Wanying JiaDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Yong LiuInstitute of Neurobiology, Environment and Genes Related to Diseases Key Laboratory of Chinese Ministry of Education, Xi'an Jiaotong University, Xi'an, China.
Malgorzata A GarstkaCore Research Laboratory, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0003-2896-7275
Ya GaoDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-6729-6374
Hui YuDepartment of Pediatric Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-4617-7640
Second Affiliated Hospital of Xi'an Jiaotong University · CNXi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hirschsprung disease (HSCR), one of several neurocristopathies in children, is characterized by nerve loss in the large intestine and is mainly treated by surgery, which causes severe complications. Enteric neural crest-derived cell (ENCC) transplantation is a potential therapeutic strategy; however, so far with poor efficacy. Here, we assessed whether and how fecal microbiota transplantation (FMT) could improve ENCC transplantation in a rat model of hypoganglionosis; a condition similar to HSCR, with less intestinal innervation. We found that the hypoganglionosis intestinal microenvironment negatively influenced the ENCC functional phenotype in vitro and in vivo. Combining 16S rDNA sequencing and targeted mass spectrometry revealed microbial dysbiosis and reduced short-chain fatty acid (SCFA) production in the hypoganglionic gut. FMT increased the abundance of Bacteroides and Clostridium, SCFA production, and improved outcomes following ENCC transplantation. SCFAs alone stimulated ENCC proliferation, migration, and supported ENCC transplantation. Transcriptome-wide mRNA sequencing identified MAPK signaling as the top differentially regulated pathway in response to SCFA exposure, and inhibition of MEK1/2 signaling abrogated the SCFA-mediated effects on ENCC. This study demonstrates that FMT improves cell therapy for hypoganglionosis via short-chain fatty acid metabolism-induced MEK1/2 signaling.

Indexed as

Fecal Microbiota TransplantationHirschsprung DiseaseAnimalsCell- and Tissue-Based TherapyFatty Acids, VolatileRatsSignal TransductionFatty Acids, Volatileenteric neural crest-derived cellsfecal transplantationHirschsprung diseasemicrobiotashort-chain fatty acids

Identifiers

PMID36382711
PMCPMC9811615
OpenAlexW4309166806

What OpenQuestion holds

Textmetadata
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.