I. Castagliuolo et al., COLONIC MUCIN RELEASE IN RESPONSE TO IMMOBILIZATION STRESS IS MAST-CELL DEPENDENT, American journal of physiology: Gastrointestinal and liver physiology, 37(6), 1998, pp. 1094-1100
We recently reported that immobilization stress increased colonic moti
lity, mucin, and prostaglandin E-2 (PGE(2)) release and mucosal mast c
ell degranulation in rat colon [Proc. Natl. Acad. Sci. USA 93: 12611-1
2615, 1996; Am. J. Physiol. 271 (Gastrointest. Liver Physiol. 34): G88
4-G892, 1996]. To directly assess the contribution of mast cells, we c
ompared colonic responses to stress in mast cell-deficient Kit(W)/Kit(
W-v) and normal (+/+) mice. Mucin and PGE(2) release were measured in
colonic explants cultured from Kit(W)/Kit(W-v) and (+/+) mice 30 min a
fter immobilization stress. We found that stress stimulated colonic mu
cin release (1.8-fold), goblet cell depletion (3-fold), and PGE(2) (2.
3-fold) release in (+/+) but not mast cell-deficient Kit(W)/Kit(W-v) m
ice. However, mast cell-deficient mice that had their mast cell popula
tion reconstituted by injection of bone marrow-derived mast cells from
(+/+) mice had colonic responses to stress similar to those of normal
(+/+) mice. In contrast, colonic transit changes in response to stres
s, estimated by fecal output, were similar between Kit(W)/Kit(W-v) and
normal (+/+) mice. We conclude that mast cells regulate colonic mucin
and PGE(2) release but not colonic transit changes in responsetom imm
unobilization stress.