2007
DOI: 10.1080/00365520600976266
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Expression of the genesdualoxidase2,lipocalin 2andregenerating islet-derived 1 alphain Crohn's disease

Abstract: As compared with controls, non-inflamed colonic mucosal cells contain two up-regulated genes related to the innate immune system. Up-regulation of these genes, known to be induced by microorganisms, suggests either increased microflora antigenicity or an altered function in mucosal barrier defence.

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Cited by 41 publications
(32 citation statements)
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“…In conclusion, upregulation of DUOX2 seems to be linked to inflammatory bowel diseases, supporting previous reports on differential expression of NOX/DUOX family members in Crohn's disease and Helicobacter pylori-induced intestinal inflammation (Csillag et al, 2007;Rokutan et al, 2008;Szanto et al, 2005).…”
Section: Expression Of Duox2 In Intestinal Epithelial Cellssupporting
confidence: 73%
“…In conclusion, upregulation of DUOX2 seems to be linked to inflammatory bowel diseases, supporting previous reports on differential expression of NOX/DUOX family members in Crohn's disease and Helicobacter pylori-induced intestinal inflammation (Csillag et al, 2007;Rokutan et al, 2008;Szanto et al, 2005).…”
Section: Expression Of Duox2 In Intestinal Epithelial Cellssupporting
confidence: 73%
“…The source of epithelial ROS was identified only a few years ago, after initial discovery of prominent expression of the NOX homologs DUOX1 and DUOX2 within the lung (35), and studies on lung tissues using in situ hybridization and immunohistochemistry, which revealed the presence of DUOX1 at the apical surface of tracheobronchial epithelial cells, and DUOX2 within salivary and submucosal glands (19,79,83,84 (88,89), which is due to the presence of DUOX1 (90). Although DUOX expression in the lung is primarily localized to airway or alveolar epithelial cells, recent studies have also suggest the presence of DUOX proteins in lymphocytes (51,91).…”
Section: Nadph Oxidases Within the Airway Epithelium: Duox1 And Duox2mentioning
confidence: 99%
“…The PCR reactions were run using the LightCycler PCR system (Roche, Manheim, Germany) as previously described. 18 To standardize the reactions, a serial 10-fold dilution of gel-purified PCR product of 1 mL was used as template in independent reactions, and the number of target molecules was calculated based on the standard curve. The number of ribosomal protein L10 transcripts (RPL10) was used for normalization between samples, as RPL10 was found constitutively and equally expressed in the microarray data from the 4 groups (calculated for probe set ID: "221989_at."…”
Section: Real-time Reverse Transcription Polymerase Chain Reactionmentioning
confidence: 99%