Evidence map›Paper›PMID 33040455›Full record

ArticleAging cell2020

Elevated miR-124-3p in the aging colon disrupts mucus barrier and increases susceptibility to colitis by targeting T-synthase.

Li Huang, Ting-Yi Sun, Liang-Jun Hu, Shi-Long Hu, Hai-Mei Sun, Fu-Qian Zhao, Bo Wu, Shu Yang, Feng-Qing Ji, De-Shan Zhou

Abstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. The landscape of aging.Science China. Life sciences · 2022
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

10 authors.

Li HuangDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Ting-Yi SunDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.ORCID 0000-0003-4448-6340
Liang-Jun HuDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shi-Long HuDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Hai-Mei SunDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Fu-Qian ZhaoDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Bo WuDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shu YangDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Feng-Qing JiDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
De-Shan ZhouDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The risk of colitis and colorectal cancer increases markedly throughout adult life, endangering the health and lives of elderly individuals. Previous studies have proposed that bacterial translocation and infection are the main risk factors for these diseases. Therefore, in the present study, we aimed to identify the underlying mechanism by focusing on the mucus barrier function and mucin-type O-glycosylation. We evaluated alterations in the colon mucus layer in 2-, 16-, and 24-month-old mice and aged humans. Aged colons showed defective intestinal mucosal barrier and changed mucus properties. The miR-124-3p expression level was significantly increased in the aged distal colonic mucosa, which was accompanied by an increase in pathogens and bacterial translocation. Meanwhile, T-synthase, the rate-limiting enzyme in O-glycosylation, displayed an age-related decline in protein expression. Further experiments indicated that miR-124-3p modulated O-glycosylation by directly targeting T-synthase. Moreover, young mice overexpressing miR-124-3p exhibited abnormal glycosylation, early-onset, and more severe colitis. These data suggest that miR-124-3p predisposes to senile colitis by reducing T-synthase, and the miR-124-3p/T-synthase/O-glycans axis plays an essential role in maintaining the physiochemical properties of colonic mucus and intestinal homeostasis.

Indexed as

Age FactorsColitisColonFemaleGalactosyltransferasesHumansIntestinal MucosaMaleMicroRNAsMucusC1GALT1 protein, humanGalactosyltransferasesMicroRNAsMIRN124 microRNA, humanagingcolitisglycosyltransferasemicroRNAmucus

Identifiers

PMID33040455
PMCPMC7681053

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.