Evidence map›Paper›PMID 33622250›Full record

ArticleCellular & molecular biology letters2021

The NOTCH-HES-1 axis is involved in promoting Th22 cell differentiation.

Chong Zeng, Zhongbao Shao, Zibo Wei, Jie Yao, Weidong Wang, Liang Yin, Huixian YangOu, Dan Xiong

Open access · goldAbstract readLetter
In one paragraph

Article in Cellular & molecular biology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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  4. Liver organoid culture methods.Cell & bioscience · 2023
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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 2 institutions in 1 country.

Chong ZengMedical Research Center, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China. wonder10@126.com.
Zhongbao ShaoDepartment of Electronic Information Engineering, Guangzhou College of Technology and Business, Foshan, China.
Zibo WeiMedical Research Center, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China.
Jie YaoMedical Research Center, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China.
Weidong WangDepartment of Hepatobiliary Surgery, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China.
Liang YinDepartment of Endocrinology, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China.
Huixian YangOuDepartment of Anesthesiology Operating Room, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, 528300, China.
Dan XiongDepartment of Hematology, Shunde Hospital, Southern Medical University (The First People's Hospital of Shunde), Foshan, Guangdong, China. xiongdancn@aliyun.com.
The First People's Hospital of Shunde · CNSouthern Medical University · CN

Funding

Medical Scientific Research Foundation of Guangdong Province A2020175
6 · The paper itself

Abstract

backgroundNOTCH signaling has been shown to play a role in the production of interleukin-22 (IL-22) by CD4

methodsIn vitro combination of IL-6, IL-23, and tumor necrosis factor-α (TNF-α) treatment with naïve CD4

resultsWe observed that the proportion of Th22 cells, along with Hes-1, Ahr, and Il-22 mRNA and protein expression, was increased by both jagged-1 and overexpression of HES-1. On the other hand, after the combined cytokine treatment of cells, and exposure to jagged-1 and DAPT or HES-1 siRNA, there was a decrease in the Th22 cell proportion, mRNA and protein expression of HES-1, AHR, and IL-22.

conclusionsOur study demonstrates that HES-1 enhancement in AHR and IL-22 up-regulation of NOTCH signaling can promote the skewing of naïve CD4

Indexed as

Signal TransductionAnimalsCell DifferentiationCell PolarityInterleukin-22InterleukinsMaleMiceMice, Inbred C57BLModels, BiologicalReceptors, NotchT-Lymphocytes, Helper-InducerTranscription Factor HES-1Hes1 protein, mouseInterleukin-22InterleukinsReceptors, NotchTranscription Factor HES-1CD4+ T cellsDifferentiationHES-1NOTCH signalingTh22

Identifiers

PMID33622250
PMCPMC7901075
OpenAlexW3131315926

What OpenQuestion holds

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LicenceCC BY
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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.