Evidence map›Paper›PMID 17660297›Full record

ArticleThe Journal of biological chemistry2007

A cellular micro-RNA, let-7i, regulates Toll-like receptor 4 expression and contributes to cholangiocyte immune responses against Cryptosporidium parvum infection.

Xian-Ming Chen, Patrick L Splinter, Steven P O'Hara, Nicholas F LaRusso

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 235 papers.

0numbers the graph read from it
0cells of the map it votes in
235citing papers in PubMed
14.8field-weighted citation impact, top 1% 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

235 citing papers in PubMed, 481 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Review
  5. Article
  6. Let-7 Family as a Mediator of Exercise on Alzheimer's Disease.Cellular and molecular neurobiology · 2025
    Review
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  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
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  17. iScience · 2023
    Article
  18. Article
  19. LetZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  20. Article

175 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Xian-Ming ChenMiles and Shirley Fiterman Center for Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905. Electronic address: xianmingchen@creighton.edu.
Patrick L SplinterMiles and Shirley Fiterman Center for Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905.
Steven P O'HaraMiles and Shirley Fiterman Center for Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905.
Nicholas F LaRussoMiles and Shirley Fiterman Center for Digestive Diseases, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905. Electronic address: larusso.nicholas@mayo.edu.
Mayo Clinic in Arizona · USMayo Clinic · US

Funding

The Pathobiology of Hepatic EpitheliaR01DK024031 · NIDDK · MAYO CLINIC ROCHESTER · PI LARUSSO, NICHOLAS F. · 1986 to 2023
$10.4M
Pathophysiology of Biliary DiseaseR01DK057993 · NIDDK · MAYO CLINIC ROCHESTER · PI LARUSSO, NICHOLAS F., O'HARA, STEVEN P · 2001 to 2025
$7.1M
MicroRNAs in Epithelial Innate Immunity to C. parvumR01AI071321 · NIAID · MAYO CLINIC ROCHESTER · PI CHEN, XIAN-MING · 2006 to 2010
$1.3M
PATHOBIOLOGY OF HEPATIC EPITHELIAR37DK024031 · NIDDK · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI LARUSSO, NICHOLAS F. · 1991 to 1998
–
NIAID NIH HHS AI071321NIAID NIH HHS R01 AI071321NIDDK NIH HHS DK24031NIDDK NIH HHS DK57993NIDDK NIH HHS R01 DK024031NIDDK NIH HHS R01 DK057993
6 · The paper itself

Abstract

Toll-like receptors (TLRs) are important pathogen recognition molecules and are key to epithelial immune responses to microbial infection. However, the molecular mechanisms that regulate TLR expression in epithelia are obscure. Micro-RNAs play important roles in a wide range of biological events through post-transcriptional suppression of target mRNAs. Here we report that human biliary epithelial cells (cholangiocytes) express let-7 family members, micro-RNAs with complementarity to TLR4 mRNA. We found that let-7 regulates TLR4 expression via post-transcriptional suppression in cultured human cholangiocytes. Infection of cultured human cholangiocytes with Cryptosporidium parvum, a parasite that causes intestinal and biliary disease, results in decreased expression of primary let-7i and mature let-7 in a MyD88/NF-kappaB-dependent manner. The decreased let-7 expression is associated with C. parvum-induced up-regulation of TLR4 in infected cells. Moreover, experimentally induced suppression or forced expression of let-7i causes reciprocal alterations in C. parvum-induced TLR4 protein expression, and consequently, infection dynamics of C. parvum in vitro. These results indicate that let-7i regulates TLR4 expression in cholangiocytes and contributes to epithelial immune responses against C. parvum infection. Furthermore, the data raise the possibility that micro-RNA-mediated post-transcriptional pathways may be critical to host-cell regulatory responses to microbial infection in general.

Indexed as

Immunity, InnateAnimalsBile DuctsCells, CulturedCryptosporidiosisCryptosporidium parvumEpithelial CellsHumansMicroRNAsMyeloid Differentiation Factor 88NF-kappa BRNA, MessengerToll-Like Receptor 4Up-RegulationMicroRNAsmirnlet7 microRNA, humanMYD88 protein, humanMyeloid Differentiation Factor 88NF-kappa BRNA, MessengerTLR4 protein, humanToll-Like Receptor 4

Identifiers

PMID17660297
PMCPMC2194650
OpenAlexW2119013116

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.