TY - JOUR
T1 - Regulation of clusterin expression in mammary epithelial cells
AU - Itahana, Yoko
AU - Piens, Marie
AU - Sumida, Tomoki
AU - Fong, Sylvia
AU - Muschler, John
AU - Desprez, Pierre Yves
N1 - Funding Information:
The authors wish to thank Drs. Jarnail Singh and Lynn Weir for helpful scientific discussions. This work was supported by grants from the California Breast Cancer Research Program (7WB-0026) and the National Institutes of Health-National Cancer Institute (RO1 CA82548) to PYD.
PY - 2007/3/10
Y1 - 2007/3/10
N2 - Mammary epithelial cells undergo changes in growth, invasion, differentiation, and dedifferentiation throughout much of adult hood, and most strikingly during pregnancy, lactation, and involution. Clusterin is a multifunctional glycoprotein that is involved in the differentiation and morphogenesis of epithelia, and that is important in the regulation of postnatal mammary gland development. However, the mechanisms that regulate clusterin expression are still poorly understood. Here, we show that clusterin is up-regulated twice during mouse mammary gland development, a first time at the end of pregnancy and a second time at the beginning of the involution. These points of clusterin up-regulation coincide with the dramatic phenotypic and functional changes occurring in the mammary gland. Using cell culture conditions that resemble the regulatory microenvironment in vivo, we determined that the factors responsible for the first up-regulation of clusterin levels can include the extracellular matrix component, laminin, and the lactogenic hormones, prolactin and hydrocortisone. On the other hand, the second and most dramatic up-regulation of clusterin can be due to the potent induction by TGF-β1, and this up-regulation by TGF-β1 is dependent on β1 integrin ligand-binding activity. Moreover, the level of expression of β-casein, a marker of mammary epithelial cell differentiation, was decreased upon treatment of cells with clusterin siRNA. Overall, these findings reveal several novel pathways for the regulation of clusterin expression during mammary gland development, and suggest that clusterin is a morphogenic factor that plays a key role during differentiation.
AB - Mammary epithelial cells undergo changes in growth, invasion, differentiation, and dedifferentiation throughout much of adult hood, and most strikingly during pregnancy, lactation, and involution. Clusterin is a multifunctional glycoprotein that is involved in the differentiation and morphogenesis of epithelia, and that is important in the regulation of postnatal mammary gland development. However, the mechanisms that regulate clusterin expression are still poorly understood. Here, we show that clusterin is up-regulated twice during mouse mammary gland development, a first time at the end of pregnancy and a second time at the beginning of the involution. These points of clusterin up-regulation coincide with the dramatic phenotypic and functional changes occurring in the mammary gland. Using cell culture conditions that resemble the regulatory microenvironment in vivo, we determined that the factors responsible for the first up-regulation of clusterin levels can include the extracellular matrix component, laminin, and the lactogenic hormones, prolactin and hydrocortisone. On the other hand, the second and most dramatic up-regulation of clusterin can be due to the potent induction by TGF-β1, and this up-regulation by TGF-β1 is dependent on β1 integrin ligand-binding activity. Moreover, the level of expression of β-casein, a marker of mammary epithelial cell differentiation, was decreased upon treatment of cells with clusterin siRNA. Overall, these findings reveal several novel pathways for the regulation of clusterin expression during mammary gland development, and suggest that clusterin is a morphogenic factor that plays a key role during differentiation.
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U2 - 10.1016/j.yexcr.2006.12.010
DO - 10.1016/j.yexcr.2006.12.010
M3 - Article
C2 - 17274979
AN - SCOPUS:33847041502
SN - 0014-4827
VL - 313
SP - 943
EP - 951
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 5
ER -