Transcriptional profiling of mammary gland side population cells

被引:42
作者
Behbod, Fariba
Xian, Wa
Shaw, Chad A.
Hilsenbeck, Susan G.
Tsimelzon, Anna
Rosen, Jeffrey M.
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Breast Ctr, Houston, TX 77030 USA
关键词
mammary gland side population cells; murine and human; microarray gene profiling;
D O I
10.1634/stemcells.2005-0375
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Similar to the bone marrow, the mammary gland contains a distinct population of Hoechst-effluxing side population cells, mammary gland side population cells (MG-SPs). To better characterize MG-SPs, their microarray gene profiles were compared to the remaining cells, which retain Hoechst dye (mammary gland non-side population cells [MG-NSPs]). For analysis, Gene Ontology (GO) that describes genes in terms of biological processes and Ontology Traverser (OT) that performs enrichment analysis were used. OT showed that MG-SP-specific genes were enriched in the GO categories of cell cycle regulation and checkpoints, multidrug-resistant transporters, organogenesis, and vasculogenesis. The MG-NSP-upregulated genes were enriched in the GO category of cellular organization and biogenesis, which includes basal epithelial markers, p63, smooth muscle actin, myosin, alpha 6 integrin, cytokeratin (CK) 14, and luminal markers CK8 and CD24. Additional studies showed that a higher percentage of MG-SPs exist in the G1 phase of the cell cycle compared with the MG-NSPs. G1 cell cycle block of MG-SPs may be explained by higher expression of cell cycle-negative regulatory genes such as transforming growth factor-beta 2, insulin-like growth factor binding protein-5, P18(INK4C), and wingless-5a (Wnt-5a). Accordingly, a smaller percentage of MG-SPs expressed nuclear beta-catenin, possibly as a consequence of the higher expression of Wnt-5a. In conclusion, microarray gene profiling suggests that MG-SPs are a lineage-deficient mammary gland subpopulation expressing key genes involved in cell cycle regulation, development, and angiogenesis.
引用
收藏
页码:1065 / 1074
页数:10
相关论文
共 65 条
[1]  
Alvi AJ, 2003, BREAST CANCER RES, V5, DOI [10.1186/bcr563, 10.1186/bcr547]
[2]   Myogenic specification of side population cells in skeletal muscle [J].
Asakura, A ;
Seale, P ;
Girgis-Gabardo, A ;
Rudnicki, MA .
JOURNAL OF CELL BIOLOGY, 2002, 159 (01) :123-134
[3]   Tissue repair and stem cell renewal in carcinogenesis [J].
Beachy, PA ;
Karhadkar, SS ;
Berman, DM .
NATURE, 2004, 432 (7015) :324-331
[4]   Direct identification and enrichment of retinal stem cells/progenitors by Hoechst dye efflux assay [J].
Bhattacharya, S ;
Jackson, JD ;
Das, AV ;
Thoreson, WB ;
Kuszynski, C ;
James, J ;
Joshi, S ;
Ahmad, I .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (06) :2764-2773
[5]   DIVERSITY OF FUNCTION IS INHERENT IN MATRICELLULAR PROTEINS - AN APPRAISAL OF THROMBOSPONDIN-1 [J].
BORNSTEIN, P .
JOURNAL OF CELL BIOLOGY, 1995, 130 (03) :503-506
[6]   A putative human breast stem cell population is enriched for steroid receptor-positive cells [J].
Clarke, RB ;
Spence, K ;
Anderson, E ;
Howell, A ;
Okano, H ;
Potten, CS .
DEVELOPMENTAL BIOLOGY, 2005, 277 (02) :443-456
[7]   Growth and differentiation of progenitor/stem cells derived from the human mammary gland [J].
Clayton, H ;
Titley, I ;
Vivanco, MD .
EXPERIMENTAL CELL RESEARCH, 2004, 297 (02) :444-460
[8]   Endothelial signaling during development [J].
Cleaver, O ;
Melton, DA .
NATURE MEDICINE, 2003, 9 (06) :661-668
[9]  
DasGupta R, 1999, DEVELOPMENT, V126, P4557
[10]   Tumour stem cells and drug resistance [J].
Dean, M ;
Fojo, T ;
Bates, S .
NATURE REVIEWS CANCER, 2005, 5 (04) :275-284