TY - JOUR
T1 - Calmodulin controls liver proliferation via interactions with C/EBPβ-LAP and C/EBPβ-LIP
AU - Orellana, Daniel
AU - Liu, Xiaoying
AU - Wang, Gou Li
AU - Jin, Jingling
AU - Iakova, Polina
AU - Timchenko, Nikolai A.
PY - 2010/7/23
Y1 - 2010/7/23
N2 - A truncated isoform of C/EBPβ, C/EBPβ-LIP, is required for liver proliferation. This isoform is expressed at high levels in proliferating liver and in liver tumors. However, high levels of C/EBPβ-LIP are also observed in non-proliferating livers during acute phase response (APR). In this paper we present mechanisms by which liver regulates activities of C/EBPβ-LIP. We found that calmodulin (CaM) inhibits the ability of C/EBPβ-LIP to promote liver proliferation during APR through direct interactions. This activity of CaM is under negative control of Ca2+, which is reduced in nuclei of livers with APR, whereas it is increased in nuclei of proliferating livers. A mutant CaM, which does not interact with C/EBPβ-LIP, also fails to inhibit the growth promotion activity of C/EBPβ-LIP. Down-regulation of CaM in livers of LPS-treated mice causes liver proliferation via activation of C/EBPβ-LIP. Overexpression of C/EBPβ-LIP above levels of CaM also initiates liver proliferation in LPStreated mice. In addition,CaMregulates transcriptional activity of another isoform of C/EBPβ, C/EBPβ-LAP, and might control liver biology through the regulation of both isoforms of C/EBPβ. In searching for molecular mechanisms by which C/EBPβ-LIP promotes cell proliferation, we found that C/EBPβ-LIP releases E2F·Rb-dependent repression of cell cycle genes by a disruption of E2F1·Rb complexes and by a direct interaction with E2F-dependent promoters. CaM inhibits these growth promotion activities of C/EBPβ-LIP and, therefore, supports liver quiescence. Thus, our findings discover a new pathway of the regulation of liver proliferation that involves calcium-CaM signaling.
AB - A truncated isoform of C/EBPβ, C/EBPβ-LIP, is required for liver proliferation. This isoform is expressed at high levels in proliferating liver and in liver tumors. However, high levels of C/EBPβ-LIP are also observed in non-proliferating livers during acute phase response (APR). In this paper we present mechanisms by which liver regulates activities of C/EBPβ-LIP. We found that calmodulin (CaM) inhibits the ability of C/EBPβ-LIP to promote liver proliferation during APR through direct interactions. This activity of CaM is under negative control of Ca2+, which is reduced in nuclei of livers with APR, whereas it is increased in nuclei of proliferating livers. A mutant CaM, which does not interact with C/EBPβ-LIP, also fails to inhibit the growth promotion activity of C/EBPβ-LIP. Down-regulation of CaM in livers of LPS-treated mice causes liver proliferation via activation of C/EBPβ-LIP. Overexpression of C/EBPβ-LIP above levels of CaM also initiates liver proliferation in LPStreated mice. In addition,CaMregulates transcriptional activity of another isoform of C/EBPβ, C/EBPβ-LAP, and might control liver biology through the regulation of both isoforms of C/EBPβ. In searching for molecular mechanisms by which C/EBPβ-LIP promotes cell proliferation, we found that C/EBPβ-LIP releases E2F·Rb-dependent repression of cell cycle genes by a disruption of E2F1·Rb complexes and by a direct interaction with E2F-dependent promoters. CaM inhibits these growth promotion activities of C/EBPβ-LIP and, therefore, supports liver quiescence. Thus, our findings discover a new pathway of the regulation of liver proliferation that involves calcium-CaM signaling.
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U2 - 10.1074/jbc.M110.129825
DO - 10.1074/jbc.M110.129825
M3 - Article
C2 - 20498378
AN - SCOPUS:77954944236
SN - 0021-9258
VL - 285
SP - 23444
EP - 23456
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 30
ER -