During microbial colonization of germfree (GF) rats, mucin releasing c
ells proliferate and upregulate their mucin synthesis. The present stu
dy determines the effect of lipopolysaccharide (LPS) as a bacterial ce
ll membrane constituent for this development. Increasing quantities of
LPS from E. coli O:55 B:5 (3.5 to 350 mu g/100 g body weight (bw)) we
re applied perorally to GF rats (AS/Ztm). One day after challenge, LPS
concentrations up to 35 mu g LPS/100 g bw had generated a dose-depend
ent hypertrophy and hyperplasia of mucin secreting cells. A further pr
oliferative response was determined in the proximal colon after applic
ation of 350 mu g LPS/100 g bw, the distal colon displayed a lesser re
activity. Epithelial lesions were observed in both levels. Five days a
fter challenge, the histological phenomena were considerably reduced.
All sections of challenged animals evidenced mononuclear cell infiltra
tions. Secreted mucins were isolated and separated into adherent and l
uminal mucin constituents, respectively. An application of 3.5 and 35
mu g LPS/100 g bw stimulated the secretion of both constituents, the l
atter ones in a more pronounced manner. The application of 350 mu g LP
S/100 g bw rendered a submaximal release of both mucin constituents. R
esults suggest a stimulating effect of LPS on mucin secreting cells an
d mucin release, most probably generated by mononuclear cells.