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Erschienen in: Pediatric Surgery International 12/2014

01.12.2014 | Original Article

Dynamic pathology for circulating free DNA in a dextran sodium sulfate colitis mouse model

verfasst von: Yuhki Koike, Keiichi Uchida, Koji Tanaka, Shozo Ide, Kohei Otake, Yoshiki Okita, Mikihiro Inoue, Toshimitsu Araki, Akira Mizoguchi, Masato Kusunoki

Erschienen in: Pediatric Surgery International | Ausgabe 12/2014

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Abstract

Purpose

In sepsis, circulating free DNA (cf-DNA) is increased, and is a marker of severity and prognosis of septic patients. This study aimed to evaluate cf-DNA in a dextran sodium sulfate-induced colitis mouse model, and its clinical implications.

Methods

Dynamic pathology of the cecum wall in the DSS-induced colitis mouse model was analyzed using multiphoton microscopy (MPM). Plasma cf-DNA concentrations in colitis mouse were quantified using PicoGreen dsDNA Assay Kit. Plasma cf-DNA was also measured in 123 human ulcerative colitis (UC) patients [mean age: 35.9 years (3–75 years) with 20 pediatric patients] to assess its relationships with clinical severity and Matt’s grade.

Results

Real-time images of cf-DNA were detected in the colitis model. The amount of labeled cf-DNA in the circulation of the colitis mice group was significantly higher compared with that in the control group (P < 0.05). In human UC blood samples, plasma cf-DNA concentrations in UC patients were significantly positively correlated with the clinical severity of UC and Matt’s grade (P < 0.05, P < 0.05, respectively).

Conclusions

Using MPM, we observed and analyzed real-time images of cf-DNA in a colitis mouse model. Plasma cf-DNA is a potential non-invasive blood marker for reflecting clinical severity and mucosal damage in UC patients.
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Metadaten
Titel
Dynamic pathology for circulating free DNA in a dextran sodium sulfate colitis mouse model
verfasst von
Yuhki Koike
Keiichi Uchida
Koji Tanaka
Shozo Ide
Kohei Otake
Yoshiki Okita
Mikihiro Inoue
Toshimitsu Araki
Akira Mizoguchi
Masato Kusunoki
Publikationsdatum
01.12.2014
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Surgery International / Ausgabe 12/2014
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-014-3607-6

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