Evidence map›Paper›PMID 19075026›Full record

ArticleInfection and immunity2009

Biphasic modulation of apoptotic pathways in Cryptosporidium parvum-infected human intestinal epithelial cells.

Jin Liu, Mingqi Deng, Cheryl A Lancto, Mitchell S Abrahamsen, Mark S Rutherford, Shinichiro Enomoto

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

44 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
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  3. Deciphering Host-Pathogen Interactions: Role ofPathogens (Basel, Switzerland) · 2025
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  4. mBio · 2024
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Role of Cryptosporidium spp in Development of Colorectal Cancer.Asian Pacific journal of cancer prevention : APJCP · 2023
    Article
  11. Artificial Infestation ofInternational journal of molecular sciences · 2023
    Article
  12. Article
  13. Early immune and host cell responses toFrontiers in parasitology · 2023
    Article
  14. Apoptotic changes in the intestinal epithelium ofJournal of parasitic diseases : official organ of the Indian Society for Parasitology · 2022
    Article
  15. Article
  16. Article
  17. IsFood and waterborne parasitology · 2022
    Article
  18. Article
  19. Article
  20. The Mucosal Innate Immune Response toFrontiers in cellular and infection microbiology · 2021
    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

6 authors at 1 institution in 1 country.

Jin LiuDepartment of Veterinary and Biomedical Sciences, University of Minnesota, 1988 Fitch Ave., No. 295, St. Paul, MN 55108, USA.
Mingqi Deng
Cheryl A Lancto
Mitchell S Abrahamsen
Mark S Rutherford
Shinichiro Enomoto
University of Minnesota · US

Funding

Host specificity of Cryptosporidium gene expressionR01AI065246 · NIAID · UNIVERSITY OF MINNESOTA · PI RUTHERFORD, MARK STEPHEN · 2006 to 2009
$1.9M
NIAID NIH HHS R01 AI065246NIAID NIH HHS R01-AI065246-02
6 · The paper itself

Abstract

The impact of Cryptosporidium parvum infection on host cell gene expression was investigated by microarray analysis with an in vitro model using human ileocecal HCT-8 adenocarcinoma cells. We found changes in 333 (2.6%) transcripts at at least two of the five (6, 12, 24, 48, and 72 h) postinfection time points. Fifty-one of the regulated genes were associated with apoptosis and were grouped into five clusters based on their expression patterns. Early in infection (6 and 12 h), genes with antiapoptotic roles were upregulated and genes with apoptotic roles were downregulated. Later in infection (24, 48, and 72 h), proapoptotic genes were induced and antiapoptotic genes were downregulated, suggesting a biphasic regulation of apoptosis: antiapoptotic state early and moderately proapoptotic state late in infection. This transcriptional profile matched the actual occurrence of apoptosis in the infected cultures. Apoptosis was first detected at 12 h postinfection and increased to a plateau at 24 h, when 20% of infected cells showed nuclear condensation. In contrast, experimental silencing of Bcl-2 induced apoptosis in 50% of infected cells at 12 h postinfection. This resulted in a decrease in the infection rate and a reduction in the accumulation of meront-containing cells. To test the significance of the moderately proapoptotic state late in the infection, we inhibited apoptosis using pancaspase inhibitor Z-VAD-FMK. This treatment also affected the progression of C. parvum infection, as reinfection, normally seen late (24 h to 48 h), did not occur and accumulation of mature meronts was impaired. Control of host apoptosis is complex and crucial to the life of C. parvum. Apoptosis control has at least two components, early inhibition and late moderate promotion. For a successful infection, both aspects appear to be required.

Indexed as

AnimalsApoptosisCaspase InhibitorsCell Line, TumorCryptosporidium parvumEpithelial CellsGene Expression ProfilingGene Expression RegulationGenes, bcl-2Gene SilencingHumansIntestinal MucosaTime FactorsCaspase Inhibitors

Identifiers

PMID19075026
PMCPMC2632021
OpenAlexW2117043829

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.