A C‐type lectin receptor pathway is responsible for the pathogenesis of acute cyclophosphamide‐induced cystitis in mice. (December 2013)
- Record Type:
- Journal Article
- Title:
- A C‐type lectin receptor pathway is responsible for the pathogenesis of acute cyclophosphamide‐induced cystitis in mice. (December 2013)
- Main Title:
- A C‐type lectin receptor pathway is responsible for the pathogenesis of acute cyclophosphamide‐induced cystitis in mice
- Authors:
- Dejima, Takashi
Shibata, Kensuke
Yamada, Hisakata
Takeuchi, Ario
Hara, Hiromitsu
Eto, Masatoshi
Naito, Seiji
Yoshikai, Yasunobu - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="mim12100-sec-0001" sec-type="section"> <p>Hemorrhagic cystitis often arises after cyclophosphamide (CYP) administration. As yet, however, the mechanism involved in its pathogenesis is unknown. In this study, it was found that the Fc receptor γ chain (FcRγ)‐ caspase recruitment domain‐containing protein 9 (CARD9)‐dependent pathway rather than the myeloid differentiation primary response gene 88 (MyD88)‐dependent pathway is involved in the pathogenesis of acute CYP‐induced cystitis in mice. Rapid and transient production of interleukin (IL)‐6 and IL‐1β was detected in the bladder at 4 hr, preceding IL‐23 and IL‐17A production and an influx of neutrophils, which reached a peak at 24 hr after injection. As assessed by weight, edema and neutrophil infiltration, cystitis was significantly attenuated in CARD9 knockout (KO) and FcRγKO mice, this attenuation being accompanied by impaired production of IL‐1β, IL‐6, IL‐23 and IL‐17A. The major source of IL‐17A is the vesical γδ T cell population: IL‐17AKO, CδKO and Tyk2KO mice showed little IL‐17A production and reduced neutrophil infiltration in the bladder after CYP injection. These results suggest that FcRγ‐CARD9‐dependent production of proinflammatory cytokines such as IL‐1β, IL‐6, and IL‐23 and the subsequent activation of IL‐17A‐producing γδ T cells are at least partly involved in the pathogenesis of acute CYP‐induced cystitis in mice.</p> </sec><abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="mim12100-sec-0001" sec-type="section"> <p>Hemorrhagic cystitis often arises after cyclophosphamide (CYP) administration. As yet, however, the mechanism involved in its pathogenesis is unknown. In this study, it was found that the Fc receptor γ chain (FcRγ)‐ caspase recruitment domain‐containing protein 9 (CARD9)‐dependent pathway rather than the myeloid differentiation primary response gene 88 (MyD88)‐dependent pathway is involved in the pathogenesis of acute CYP‐induced cystitis in mice. Rapid and transient production of interleukin (IL)‐6 and IL‐1β was detected in the bladder at 4 hr, preceding IL‐23 and IL‐17A production and an influx of neutrophils, which reached a peak at 24 hr after injection. As assessed by weight, edema and neutrophil infiltration, cystitis was significantly attenuated in CARD9 knockout (KO) and FcRγKO mice, this attenuation being accompanied by impaired production of IL‐1β, IL‐6, IL‐23 and IL‐17A. The major source of IL‐17A is the vesical γδ T cell population: IL‐17AKO, CδKO and Tyk2KO mice showed little IL‐17A production and reduced neutrophil infiltration in the bladder after CYP injection. These results suggest that FcRγ‐CARD9‐dependent production of proinflammatory cytokines such as IL‐1β, IL‐6, and IL‐23 and the subsequent activation of IL‐17A‐producing γδ T cells are at least partly involved in the pathogenesis of acute CYP‐induced cystitis in mice.</p> </sec> </abstract> … (more)
- Is Part Of:
- Microbiology and immunology. Volume 57:Number 12(2013:Dec.)
- Journal:
- Microbiology and immunology
- Issue:
- Volume 57:Number 12(2013:Dec.)
- Issue Display:
- Volume 57, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 57
- Issue:
- 12
- Issue Sort Value:
- 2013-0057-0012-0000
- Page Start:
- 833
- Page End:
- 841
- Publication Date:
- 2013-12
- Subjects:
- Microbiology -- Periodicals
Immunology -- Periodicals
Allergy and Immunology -- Periodicals
Microbiology -- Periodicals
Microbiologie -- Périodiques
Immunologie -- Périodiques
579 - Journal URLs:
- http://bibpurl.oclc.org/web/42307 ↗
http://bibpurl.oclc.org/web/7904 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1348-0421 ↗
http://www.sanbi.co.jp/capj/ ↗
http://www3.interscience.wiley.com/journal/118902525/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1348-0421.12100 ↗
- Languages:
- English
- ISSNs:
- 0385-5600
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5757.791000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3641.xml