Journal
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
Volume 289, Issue 1, Pages G153-G162Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpgi.00395.2004
Keywords
animal models; gender differences; barrier function
Categories
Funding
- NCCIH NIH HHS [AT-01180] Funding Source: Medline
Ask authors/readers for more resources
P-glycoprotein, the product of the multidrug resistance protein 1 (MDR1) gene, is a xenobiotic transporter that may contribute to the physiology of the intestinal barrier. Twenty-five percent of mdr1a-deficient (mdr1a(-/-)) mice spontaneously develop colitis at variable ages when maintained under specific pathogen-free conditions. We hypothesized that this disease would result from epithelial dysfunction and that conventional housing would increase incidence and severity of the colitis phenotype. Wild-type congenic FVB ((+/+)) mice were maintained under the same conditions as controls. Knockout and wild-type mice were matched for age and gender and observed for signs of colitis. Colonic tissues from both groups of mice were examined for macroscopic and microscopic injury and for basal ion transport and transepithelial resistance (TER). Translocation of bacteria across the intestine was assessed by culturing the spleen and mesenteric lymph nodes. Protein analysis was performed by Western blot analysis. All mdr1a(-/-) mice developed weight loss and signs of colitis, whereas wild-type mice never showed such signs. Within the mdr1a(-/-) group, males consistently developed severe colitis earlier than females. Knockout mice showed increased basal colonic ion transport ( females, 162.7 +/- 4.6 vs. 49.7 +/- 3.8 mu A/cm(2); males, 172.6 +/- 5.6 vs. 54.2 +/- 3.1 mu A/cm(2); P < 0.01) and decreased TER ( females, 25.4 +/- 0.3 vs. 36.4 +/- 0.8 Omega center dot cm(2); males, 23.1 +/- 1.0 vs. 38.3 +/- 0.2 Omega center dot cm2; P < 0.01) compared with wild-type mice. Barrier dysfunction was accompanied by decreased phosphorylation of tight junction proteins. Expression of cyclooxygenase-2 and inducible nitric oxide synthase in intestinal tissues was increased in the mdr1a(-/-) group ( P < 0.01) and correlated with disease severity. Bacterial translocation was greater both in incidence ( P < 0.01) and severity ( P < 0.001) for the knockout group. With respect to all indexes studied, mdr1a(-/-) males performed worse than females. Our data support the hypothesis that alterations in the intestinal barrier alone, in the absence of immune dysfunction, may rapidly lead to colitis in the setting of a normal colonic flora.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available