2002
DOI: 10.1128/iai.70.4.2090-2099.2002
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Role of Gamma Interferon in Chemokine Expression in the Ileum of Mice and in a Murine Intestinal Epithelial Cell Line afterCryptosporidium parvumInfection

Abstract: Cryptosporidium parvum is a protozoan parasite that infects intestinal epithelial cells and induces inflam-In the absence of IFN-␥, the chemokine response was altered for IP-10, MIG, i-TAC, RANTES, and MIP-1␤ mRNAs, while the three ELR C-X-C chemokine mRNAs studied (lipopolysaccharide-induced C-X-C chemokine, MIP-2␣, and KC mRNAs) were strongly overexpressed. These results are consistent with the neutrophil recruitment observed in the lamina propria of GKO mice at day 9 postinfection but are not consistent wit… Show more

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Cited by 93 publications
(84 citation statements)
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References 36 publications
(24 reference statements)
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“…(30). Immune cell functions altered in these mice include decreased activation of macrophages and NK cells, altered T-cell proliferation, and altered activation of cytokines and chemokines (14,27).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…(30). Immune cell functions altered in these mice include decreased activation of macrophages and NK cells, altered T-cell proliferation, and altered activation of cytokines and chemokines (14,27).…”
Section: Methodsmentioning
confidence: 99%
“…Since the dynamic interplay between host defenses and pathogens cannot be completely mimicked by cell culture systems, animal infection models provide valuable insights into how virulence factors thwart host defenses and reveal interactions among host defenses during infection (8,25,27,36,47). We previously reported differences in the levels of attenuation of yopE and yopH mutants in single-strain mouse infections compared to competition infections with wild-type Y. pseudotuberculosis (30).…”
mentioning
confidence: 99%
“…published primers for cDNA amplification of chemokines (25,29,38), and their specificities and optimum PCR conditions have been described previously. To control for possible contamination of genomic DNAs in total RNA extracts, primer sequences for GAPDH were separated by introns so that the amplified products from genomic DNAs would be longer than the amplified cDNAs (38).…”
Section: Methodsmentioning
confidence: 99%
“…The first-strand cDNA was generated from 5 g of total RNA prepared as described above in a final volume of 50 l and was subjected to PCR amplification of the specific cDNA sequences by using an RNA PCR kit (AMV) and Ex Taq DNA polymerase (Takara Bio Inc., Shiga, Japan) according to the manufacturer's protocol. Oligonucleotides were synthesized on the basis of the published primers for cDNA amplification of GAPDH (glyceraldehyde-3-phosphate dehydrogenase) (68), iNOS (71), cytokines (27,36,71,72), and chemokines (68,46); their specificities and optimum PCR conditions have been described previously. To control possible contamination of genomic DNAs in total RNA extracts, primer sequences for GAPDH were separated by introns so that the amplified products from genomic DNAs would be longer than the amplified cDNAs (68).…”
Section: Methodsmentioning
confidence: 99%