Open AccessIncreased Intestinal Epithelial Cell Turnover and Intestinal Motility in Gymnophalloides seoi-Infected C57BL/6 Mice
Author(s) -
Sang Hyub Lee,
Byung Mun Jung,
JaeGwan Park,
Eun Hee Shin,
Jong Yil Chai
Publication year - 2014
Publication title -
korean journal of parasitology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.555
H-Index - 42
eISSN - 1738-0006
pISSN - 0023-4001
DOI - 10.3347/kjp.2014.52.3.273
Subject(s) - goblet cell , crypt , biology , motility , hyperplasia , cell growth , immunosuppression , intestinal mucosa , intestinal epithelium , epithelium , immunology , andrology , medicine , endocrinology , microbiology and biotechnology , biochemistry , genetics
The changing patterns of goblet cell hyperplasia, intestinal epithelial cell turnover, and intestinal motility were studied in ICR and C57BL/6 mice infected with Gymnophalloides seoi (Digenea: Gymnophallidae). Whereas ICR mice retained G. seoi worms until day 7 post-infection (PI), C57BL/6 mice showed a rapid worm expulsion within day 3 PI. Immunosuppression with Depo-Medrol significantly delayed the worm expulsion in C57BL/6 mice. Goblet cell counts were increased in both strains of mice, peaking at day 1 PI in C57BL/6 mice and slowly increasing until day 7 PI in ICR mice. In C57BL/6 mice infected with G. seoi, newly proliferating intestinal epithelial cells were remarkably increased in the crypt, and the increase was the highest at day 1 PI. However, in ICR mice, newly proliferating intestinal epithelial cells increased slowly from day 1 to day 7 PI. Intestinal motility was increased in G. seoi-infected mice, and its chronological pattern was highly correlated with the worm load in both strains of mice. Meanwhile, immunosuppression of C57BL/6 mice abrogated the goblet cell proliferation, reduced the epithelial cell proliferation, and suppressed the intestinal motility. Goblet cell hyperplasia, increased intestinal epithelial cell turnover, and increased intestinal motility should be important mucosal defense mechanisms in G. seoi-infected C57BL/6 mice.