Comparative proteomic analysis of proliferating and functionally differentiated mammary epithelial cells

被引:46
作者
Desrivières, S
Prinz, T
Laria, NCP
Meyer, M
Boehm, G
Bauer, U
Schäfer, J
Neumann, T
Shemanko, C
Groner, B
机构
[1] Georg Speyer Haus, D-60596 Frankfurt, Germany
[2] Proteome Sci Plc, Surrey KT11 3EP, England
关键词
D O I
10.1074/mcp.M300032-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proliferation and differentiation of mammary epithelial cells are governed by hormonal stimuli, cell-cell, and cell-matrix interactions. Terminal differentiation of mammary epithelial cells depends upon the action of the lactogenic hormones, insulin, glucocorticoids, and prolactin that enable them to synthesize and secrete milk proteins. These differentiated cells are polarized and carry out vectorial transport of milk constituents across the apical plasma membrane. To gain additional insights into the mechanisms governing differentiation of mammary epithelial cells, we identified proteins whose expression distinguishes proliferating from differentiated mammary epithelial cells. For this purpose we made use of the HC11 mammary epithelial line, which is capable of differentiation in response to lactogenic hormones. Using two-dimensional gel electrophoresis and mass spectrometry, we found about 60 proteins whose expression levels changed in between these two differentiation states. Bioinformatic analysis revealed differential expression of cytoskeletal components, molecular chaperones and regulators of protein folding and stability, calcium-binding proteins, and components of RNA-processing pathways. The actin cytoskeleton is asymmetrically distributed in differentiated epithelial cells, and the identification of proteins involved in mRNA binding and localization suggests that asymmetry might in part be achieved by controlling cellular localization of mRNAs. The proteins identified provide insights into the differentiation of mammary epithelial cells and the regulation of this process.
引用
收藏
页码:1039 / 1054
页数:16
相关论文
共 97 条
[91]   HEMOSTATIC, INFLAMMATORY, AND FIBROBLAST RESPONSES ARE BLUNTED IN MICE LACKING GELSOLIN [J].
WITKE, W ;
SHARPE, AH ;
HARTWIG, JH ;
AZUMA, T ;
STOSSEL, TP ;
KWIATKOWSKI, DJ .
CELL, 1995, 81 (01) :41-51
[92]   Establishing cell polarity in development [J].
Wodarz, A .
NATURE CELL BIOLOGY, 2002, 4 (02) :E39-E44
[93]   A novel growth-related nuclear protein binds and inhibits rat aldolase B gene promoter [J].
Yabuki, T ;
Miyagi, S ;
Ueda, H ;
Saitoh, Y ;
Tsutsumi, K .
GENE, 2001, 264 (01) :123-129
[94]   NMDA receptor function is regulated by the inhibitory scaffolding protein, RACK1 [J].
Yaka, R ;
Thornton, C ;
Vagts, AJ ;
Phamluong, K ;
Bonci, A ;
Ron, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) :5710-5715
[95]   The RACK1 signaling scaffold protein selectively interacts with the cAMP-specific phosphodiesterase PDE4D5 isoform [J].
Yarwood, SJ ;
Steele, MR ;
Scotland, G ;
Houslay, MD ;
Bolger, GB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (21) :14909-14917
[96]  
ZHANG LR, 1995, CANCER RES, V55, P428
[97]   Use of serological proteomic methods to find biomarkers associated with breast cancer [J].
Zhao, R ;
Ji, JG ;
Tong, YP ;
Pu, H ;
Ru, BG .
PROTEOMICS, 2003, 3 (04) :433-439