Bjw. Vanklinken et al., THE HUMAN INTESTINAL-CELL LINES CACO-2 AND LS174T AS MODELS TO STUDY CELL-TYPE-SPECIFIC MUCIN EXPRESSION, Glycoconjugate journal, 13(5), 1996, pp. 757-768
Mucin expression was studied during proliferation and differentiation
of the enterocyte-like Caco-2 and goblet cell-like LS174T cell lines.
Caco-2 cells express mRNAs of MUC1, MUC3, MUC4 and MUC5A/C whereas MUC
2 and MUC6 mRNAs are virtually absent. Furthermore, MUC3 mRNA is expre
ssed in a differentiation dependent manner, as is the case for enteroc
ytes. Concomitantly MUC3 protein precursor (similar to 550 kDa) was de
tected in Caco-2 cells. In LS174T cells mucin mRNAs of MUC1, MUC2 and
MUC6 are constitutively expressed at high levels, whereas MUC3, MUC4 a
nd MUC5A/C mRNAs are present at low levels. At the protein level LS174
T cells express the goblet cell specific mucin protein precursors MUC2
, MUC5A/C and MUC6 with apparent molecular masses of about 600 kDa, 47
0/500 kDa and 400 kDa respectively. MUC3 protein is not detectable. Fu
rthermore, human gallbladder mucin protein (similar to 470 kDa precurs
or), of which the gene has not yet been identified, is expressed in LS
174T cells. In addition, synthesis and secretion of the goblet cell sp
ecific mature MUC2, MUC5A/C and human gallbladder mucin was demonstrat
ed in LS174T cells. It is concluded that Caco-2 and LS174T cell lines
provide excellent in vitro models to elucidate the cell-type specific
mechanisms responsible for mucin expression.