Isolation of Pure Populations of Epithelial and Myoepithelial Cells from the Normal Human Mammary Gland Using Immunomagnetic Separation with Dynabeads

1995 ◽  
Vol 226 (1) ◽  
pp. 91-99 ◽  
Author(s):  
J.J. Gomm ◽  
P.J. Browne ◽  
R.C. Coope ◽  
Q.Y. Liu ◽  
L. Buluwela ◽  
...  
2002 ◽  
Vol 175 (2) ◽  
pp. 307-318 ◽  
Author(s):  
M Raccurt ◽  
PE Lobie ◽  
E Moudilou ◽  
T Garcia-Caballero ◽  
L Frappart ◽  
...  

We have demonstrated and localized human GH (hGH) gene expression in surgical specimens of normal human mammary gland and in proliferative disorders of the mammary gland of increasing severity using sensitive in situ RT-PCR methodology. hGH mRNA identical to pituitary hGH mRNA was first detected by RT-PCR of RNA derived from samples of normal human mammary gland. Cellular localization of hGH gene expression in the normal mammary gland exhibited restriction to luminal epithelial and myoepithelial cells of the ducts and to scattered stromal fibroblasts. We subsequently examined the expression of the hgh gene in three progressive proliferative disorders of the human mammary gland, i.e. A benign lesion (fibroadenoma), a pre-invasive stage (intraductal carcinoma) and an invasive ductal carcinoma. hGH mRNA was readily detected in the tumoral and non-tumoral epithelial components and also in cells of the reactive stroma including fibroblasts, myofibroblastic and myoepithelial cells, inflammatory infiltrate lymphocytes and endothelial cells in areas of neovascularization. In all three proliferative disorders examined, the intensity of the cellular labeling observed in both the epithelial and stromal compartments was always stronger compared with that in adjacent normal tissue. hGH protein was also present in significantly higher concentration in extracts derived from proliferative disorders of the mammary gland compared with extracts derived from normal mammary gland. We also examined hGH gene expression in axillary lymph nodes not containing and containing metastatic mammary carcinoma. hGH gene expression was evidenced in metastatic mammary carcinoma cells and in reactive stromal cells by both in situ hybridization and in situ RT-PCR. In contrast, in lymph nodes not containing metastatic mammary carcinoma, hGH mRNA was detected only by use of in situ RT-PCR. Thus, increased expression of the hGH gene in the epithelial component and the de novo stromal expression in proliferative disorders of the mammary gland are suggestive of a pivotal role for autocrine hGH in neoplastic progression of the mammary gland.


2021 ◽  
Vol 123 (8) ◽  
pp. 151798
Author(s):  
Mateus H.R. de Almeida ◽  
Geovana D. Savi Bortolotto ◽  
Rafael Cypriano Dutra ◽  
Gustavo Narvaes Guimarães ◽  
Francielly A. Felipetti

2018 ◽  
Vol 7 (3) ◽  
pp. 241-246
Author(s):  
Shedge Swapna A. ◽  
◽  
Priya P. Roy ◽  
Megha A. Doshi ◽  
Pratibha Patil ◽  
...  

1988 ◽  
Vol 42 (2) ◽  
pp. 147-153 ◽  
Author(s):  
V. I. Guelstein ◽  
T. A. Tchypysheva ◽  
V. D. Ermilova ◽  
L. V. Litvinova ◽  
S. M. Troyanovsky ◽  
...  

2017 ◽  
Author(s):  
Justin A. Colacino ◽  
Ebrahim Azizi ◽  
Michael D. Brooks ◽  
Shamileh Fouladdel ◽  
Sean P. McDermott ◽  
...  

AbstractDuring development and pregnancy, the human mammary gland undergoes extensive remodeling in processes driven by populations of stem and progenitor cells. We recently reported that breast cancers are also hierarchically organized and driven by distinct populations of cancer stem cells characterized as CD44+CD24low/−or by expression of Aldehyde dehydrogenase (ALDH). These sets of markers identify largely non-overlapping mesenchymal and epithelial populations, each of which is capable of tumor initiation when transplanted into immunosuppressed mice. Less is known about these two populations, individually or their overlap, in the normal human mammary gland. The goal of this study was to understand the biology of the ALDH+and CD44+CD24−populations in the normal human breast, using flow cytometry based sorting paired with functionalex vivoanalyses, RNA-sequencing, and single cell RNA expression profiling. ALDH+cells and ALDH−CD44+CD24−cells, generally, have epithelial-like and mesenchymal-like characteristics, respectively. Despite this, there are substantial similarities in the biological pathways activated in both populations when compared to differentiated cells. Additionally, we found a substantial proportion of cells that simultaneously express ALDH+and CD44+CD24−whose abundance varies between individuals. At the single cell level, these cells have the greatest mammosphere forming capacity and express high levels of stemness and EMT-associated genes includingID1, SOX2, TWIST1, and ZEB2.Through unbiased analysis of individual ALDH+ cells, we find cells with either epithelial or mesenchymal expression phenotypes. We also identify a subpopulation of cells with a hybrid epithelial/mesenchymal expression phenotype that overexpress genes associated with aggressive triple negative breast cancers. These results highlight the utility of single cell analyses to characterize tissue heterogeneity, even in marker enriched cell populations, and further identifies the genes and pathways that define this heterogeneity.


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