Expression and function of CCAAT/enhancer binding protein beta (C/EBP beta) LAP and LIP isoforms in mouse mammary gland, tumors and cultured mammary epithelial cells
Lr. Dearth et al., Expression and function of CCAAT/enhancer binding protein beta (C/EBP beta) LAP and LIP isoforms in mouse mammary gland, tumors and cultured mammary epithelial cells, J CELL BIOC, 82(3), 2001, pp. 357-370
CCAAT/Enhancer binding proteins (C/EBPs) play important roles in the regula
tion of cell growth and differentiation. This study investigated the expres
sion and function of C/EBP beta isoforms in the mouse mammary gland, mammar
y tumors, and a nontransformed mouse mammary epithelial cell line (HC11). C
/EBP beta mRNA levels are 2-5-fold higher in mouse mammary tumors derived f
rom MMTV/c-neu transgenic mice compared with lactating and involuting mouse
mammary gland. The "full-length" 38 kd C/EBP beta LAP ("Liver-enriched Act
ivator Protein") isoform is the predominant C/EBP beta protein isoform in m
ammary tumor whole cell lysates, however, the truncated 20 kd C/EBP beta LI
P ("Liver-enriched Inhibitory Protein") isoform is also present at detectab
le levels (mean LAP:LIP ratio 5.3:1). The mammary tumor C/EBP beta LAP:LIP
ratio decreases 70% (from 5.3:1 to 1.6:1) when lysate preparation is switch
ed from a rapid whole cell lysis protocol to a multistep nuclear/cytoplasmi
c fractionation protocol. In contrast to mammary tumors, only the C/EBP bet
a LAP isoform is detectable in the mammary gland whole cell and nuclear lys
ates; the truncated "LIP" isoform is undetectable regardless of isolation p
rotocol. Ectopic over expression of C/EBP beta LIP or C/EBP beta LAP did no
t alter HC11 growth rates. However, C/EBP beta LIP over expressing HC11 cel
ls (LAP:LIP ratio of similar to1:1) exhibited a consistent 2-4 h delay in G
(0)/S phase transition. C/EBP beta LIP overexpressing HC11 cells did not ex
press P-casein mRNA (mammary epithelial cel I differentiation marker) in re
sponse to lactogenic hormones. This defect in P-casein expression was not c
orrected by carrying out the differentiation protocol in the presence of an
artificial extracellular matrix. These results demonstrate that the "full-
length" C/EBP beta LAP isoform is the predominant C/EBP beta protein isofor
m expressed in mouse mammary gland in vivo and mouse mammary epithelial cel
l cultures in vitro. C/EBP beta LIP detected in mammary tumor lysates may r
esult from in vivo production or ex vivo isolation-induced proteolysis of C
/EBP beta LAP. Ectopic overexpression of C/EBP beta LIP (LAP:LIP ratio of s
imilar to1:1) inhibits mammary epithelial cell differentiation (P-casein ex
pression). (C) 2001 Wiley-Liss.