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Interleukin–18 is a crucial determinant of vulnerability of the mouse rectum to psychosocial stress
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ABSTRACT
Psychosocial factors are important determinants of disease manifestations, treatment efficacy, and prognosis of functional and inflammatory bowel disorders. Isolation of C57BL/6J mice from their 4 brothers growing in the same cage reduced goblet cells and MUC2 expression with a peak on day 8 in the rectum, but not in the colon. Gene expression analysis using a whole mouse genome microarray showed that the stress induced a 10‐fold larger change in the gene expression in the rectum (722 genes) than in the colon (72 genes). The Ingenuity Pathway Analysis (IPA) application organized the rectum‐specific 711 genes into stress response‐related pathways. Nuclearfactor‐KB‐related cytokine networks constructed with IPA showed selective up‐regulation of interleukin (IL)‐18 mRNA expression, which was also confirmed by real‐time polymerase chain reaction. The stress produced active forms of caspase 1, IL‐18, and a negative regulator for goblet cells, Notch 1, only in the rectum.IL‐18‐knockout mouse rectum had significantly increased goblet cells and MUC2 mucin, compared with wild‐type mouse rectum. The absence ofIL‐18 completely blocked the stress‐induced changes in gene expression and the goblet cell responses in the rectum. Thus,IL‐18 may be a crucial determinant for the vulnerability of the rectum to psychosocial stress.—Nishida, K.,Kamizato, M., Kawai, T., Masuda, K., Takeo, K., Teshima‐Kondo, S.,Tanahashi, T., Rokutan, K. Interleukin‐18 is a crucial determinant of vulnerability of the mouse rectum to psychosocial stress.
FASEBJ. 23
, 1797–1805 (2009)
Title: Interleukin–18 is a crucial determinant of vulnerability of the mouse rectum to psychosocial stress
Description:
ABSTRACT
Psychosocial factors are important determinants of disease manifestations, treatment efficacy, and prognosis of functional and inflammatory bowel disorders.
Isolation of C57BL/6J mice from their 4 brothers growing in the same cage reduced goblet cells and MUC2 expression with a peak on day 8 in the rectum, but not in the colon.
Gene expression analysis using a whole mouse genome microarray showed that the stress induced a 10‐fold larger change in the gene expression in the rectum (722 genes) than in the colon (72 genes).
The Ingenuity Pathway Analysis (IPA) application organized the rectum‐specific 711 genes into stress response‐related pathways.
Nuclearfactor‐KB‐related cytokine networks constructed with IPA showed selective up‐regulation of interleukin (IL)‐18 mRNA expression, which was also confirmed by real‐time polymerase chain reaction.
The stress produced active forms of caspase 1, IL‐18, and a negative regulator for goblet cells, Notch 1, only in the rectum.
IL‐18‐knockout mouse rectum had significantly increased goblet cells and MUC2 mucin, compared with wild‐type mouse rectum.
The absence ofIL‐18 completely blocked the stress‐induced changes in gene expression and the goblet cell responses in the rectum.
Thus,IL‐18 may be a crucial determinant for the vulnerability of the rectum to psychosocial stress.
—Nishida, K.
,Kamizato, M.
, Kawai, T.
, Masuda, K.
, Takeo, K.
, Teshima‐Kondo, S.
,Tanahashi, T.
, Rokutan, K.
Interleukin‐18 is a crucial determinant of vulnerability of the mouse rectum to psychosocial stress.
FASEBJ.
23
, 1797–1805 (2009).
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