Histochemical Characteristics of Mucosubstances in Normal Human Mammary Gland

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

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.


2002 ◽  
Vol 55 (5) ◽  
pp. 371-374 ◽  
Author(s):  
V Speirs ◽  
G P Skliris ◽  
S E Burdall ◽  
P J Carder

Endocrinology ◽  
2002 ◽  
Vol 143 (12) ◽  
pp. 4886-4896 ◽  
Author(s):  
Hema Parmar ◽  
Peter Young ◽  
Joanne T. Emerman ◽  
Richard M. Neve ◽  
Shanaz Dairkee ◽  
...  

Abstract A novel system is described for studying the growth of normal human mammary epithelium in vivo as grafts in athymic nude mice. The key feature of this model is reconstitution of the epithelial-stromal interactions required for normal growth and differentiation of the human mammary epithelium, which produces ducts that are comparable to those in the normal human mammary gland. Human breast epithelial organoids were combined with mammary fibroblasts from mouse or human origin in collagen gels, which were subsequently transplanted under the renal capsule of female nude mice hosts. The resulting grafts showed an increase in the ductal density compared with that observed previously. These ducts expressed appropriate markers for luminal and myoepithelial cells and steroid receptors. Treatment of the host with diethylstilbestrol or estradiol and progesterone significantly increased the number of ducts observed and increased cell proliferation. The grafts also displayed production of β-casein and milk fat globule membrane protein when the hosts were allowed to become pregnant. This model allows for a variety of epithelial and stromal cells to be used in combination, which would aid in understanding key factors that regulate normal human mammary gland development.


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