Basal cells of H-Dunning tumor are myoepithelial cells

1991 ◽  
Vol 95 (4) ◽  
pp. 341-349 ◽  
Author(s):  
G. Aum�ller ◽  
U. Gr�schel-Stewart ◽  
M. Altmannsberger ◽  
H. G. Mannherz ◽  
M. Steinhoff
Keyword(s):  
Myoepithelial Cells ◽  
Basal Cells ◽  
Dunning Tumor

Regeneration of mammary glands in vivo from isolated mammary ducts

Development ◽  
1986 ◽  
Vol 96 (1) ◽  
pp. 229-243
Author(s):  
E. Jane Ormerod ◽  
Philip S. Rudland
Keyword(s):  
Epithelial Cells ◽  
Milk Fat ◽  
Cell Types ◽  
Mammary Glands ◽  
Myoepithelial Cells ◽  
Basal Cells ◽  
Alveolar Cells ◽  
Terminal End Buds ◽  
Mammary Cell

Rat mammary ducts, free of buds, can alone regenerate complete mammary trees when transplanted into the interscapular fat pads of syngeneic host rats. All the main mammary cell types are identified within such outgrowths. Epithelial cells, which show the presence of milk fat globule membrane antigens and microvilli on their luminal surfaces, line the ducts. Basal cells surrounding the ducts show characteristic features of myoepithelial cells: immunoreactive actin and keratin within the cytoplasm, myofilaments, pinocytotic vesicles and hemidesmosomal attachments to the basement membrane. Cells within the end buds and lateral buds, however, show few if any cytoplasmic myofilaments and are relatively undifferentiated in appearance. Intermediate morphologies between these cells and myoepithelial cells are seen nearer the ducts. In this respect they exactly resemble the cap cells found in terminal end buds (TEBs) of normal mammary glands. Occasional epithelial cells within alveolar buds show the presence of immunoreactive casein, which is a product of secretory alveolar cells in the normal rat mammary gland. Dissected terminal end buds can regenerate similar ductal outgrowths. Thus, ductal tissue alone can generate all the major mammary cell types seen in the normal gland, including the cap cells.

Characterization of luminal and basal cells flow-sorted from the adult rat mammary parenchyma

1991 ◽  
Vol 100 (3) ◽  
pp. 459-471
Author(s):  
S.R. Dundas ◽  
M.G. Ormerod ◽  
B.A. Gusterson ◽  
M.J. O'Hare
Keyword(s):  
Neutral Endopeptidase ◽  
Myoepithelial Cells ◽  
Basal Cells ◽  
Proliferating Cells ◽  
Adult Rat ◽  
Morphological Criteria ◽  
Membrane Antigens ◽  
Cell Type Specific ◽  
Alpha Actin ◽  
Type 3

Differentially expressed membrane antigens have been used to flow-sort viable luminal epithelial and myoepithelial cells from freshly disaggregated adult virgin rat mammary parenchyma. Resulting cultures and clones have been characterized morphologically and by a panel of antibodies that recognise cell-type-specific cytoskeletal antigens in the intact mammary gland. Five clonal phenotypes were recognisable by morphological criteria, three (types 1–3) exclusively associated with sorted luminal epithelial (25.5-positive) cells, and two (types 4 and 5) generated from the sorted myoepithelial (CALLA/neutral endopeptidase 24.11-positive) cells. All clones derived from myoepithelial cells continued to express a basal parenchymal marker in the form of the rat equivalent of human cytokeratin 14, while smooth muscle alpha-actin was expressed by the small slowly growing type 4 clones but was found in fewer cells in rapidly proliferating type 5 myoepithelially derived clones. Two of the luminal clone types, characterized by an attenuated appearance and slow growth (types 1/2), expressed only luminal-specific markers, including the equivalent of human cytokeratins 7/18/19. Type 3 clones, by contrast, consisted of rapidly proliferating cells, many of which either co-expressed CK14 and CK18 antigens (type 3a) or were composed of a mosaic of CK14+/CK18-, CK14+/CK18+ and CK14-/CK18+ cells (type 3b). The sorted myoepithelially derived clones grew faster than clones from sorted luminal cells as evidenced by the larger fraction of cells synthesizing DNA. All types of clone could be obtained from both isolated ducts and alveoli, when these were cloned separately, although there were some differences in their relative frequency.(ABSTRACT TRUNCATED AT 250 WORDS)

Basal Cells of Second Trimester Fetal Breasts: Immunohistochemical Study of Myoepithelial Precursors

2003 ◽  
Vol 6 (5) ◽  
pp. 398-413 ◽  
Author(s):  
Francine Jolicoeur ◽  
Louis A. Gaboury ◽  
Luc L. Oligny
Keyword(s):  
Cancer Progression ◽  
Smooth Muscle Actin ◽  
Adult Life ◽  
Cell Lineage ◽  
Myoepithelial Cells ◽  
Mammary Tissue ◽  
Basal Cells ◽  
Second Trimester ◽  
Laminin 5 ◽  
Type Iv

The molecular characterization of human mammary myoepithelial cells is incomplete, hindering our understanding of its importance in breast physiology and pathology. Because data on the precursors of this cell lineage remain scarce and often contradictory, basal epithelial cells of second trimester fetal breasts were studied by light microscopy (LM) and immunohistochemistry (IHC). Up to 20 wk of gestational age, the mammary rudiments only comprised roundish primary outgrowths, “primary buds,” more likely to represent immature nipples than true mammary tissue. At 21 wk secondary outgrowths, “projections,” extended from enlarged primary buds into well-vascularized layers of dense mesenchyme. Basal projection cells had a partial myoepithelial-like phenotype: they reacted with CD29, CD49f, CD104, keratin 14, vimentin, S100β protein, and p63; furthermore, many became positive for keratin 17, α-smooth muscle actin, and CD10 (but not for keratin 19) between wk 21 and 25. The continuous basement membrane associated with the fetal mammary rudiments was strongly positive for collagens type IV and VII, and for laminin 5. Consistently strong and basally polarized staining for hemidesmosomal components suggested that although incompletely differentiated, most second trimester myoepithelial precursors might already mediate local epithelial-mesenchymal interactions, i.e., complex signaling pathways which are crucial for both orderly growth during development and maintenance of homeostasis during adult life. Because they are likely implicated in the phenomenon of menstrual cycle-related growth spurts in the adult resting breast, the strategically positioned cells of the myoepithelial lineage might constitute critical protagonists in defective epithelial-mesenchymal signaling associated with cancer progression.

scholarly journals Peanut Agglutinin Lectin Immunohistochemical Staining of Normal and Neoplastic Canine Tissues

1993 ◽  
Vol 30 (4) ◽  
pp. 333-342 ◽  
Author(s):  
D. M. Haines
Keyword(s):  
Binding Sites ◽  
Immunohistochemical Staining ◽  
Lectin Binding ◽  
Mesenchymal Cell ◽  
Myoepithelial Cells ◽  
Neoplastic Cell ◽  
Basal Cells ◽  
Peanut Agglutinin ◽  
Normal Cells ◽  
Canine Tumors

Peanut lectin binding sites were demonstrated in normal canine tissues and in 114 canine tumors by avidin biotin complex immunohistochemical staining on unfixed cryostat tissue sections. Peanut agglutinin (PNA) receptors occurred in a variety of normal cells and tissues, including lymphoid follicle center cells; cortical thymocytes; basal cells and the stratum spinosum of stratified squamous epithelium; columnar epithelium of the gastrointestinal tract; parietal cells and chief cells of the stomach; some endothelial cells; myelin; chrondrocytes; spermatogenic cells; cells of the adrenal medulla; Bowman's capsule and the distal convoluted tubules of the kidney; prostatic, perianal and endometrial epithelium; and the extracellular matrix of connective tissues. Neoplastic cell staining was sporadic and was most often observed in benign or well-differentiated neoplastic tissues in which the corresponding normal cells also expressed PNA binding sites. However, PNA also bound to some tumor cells in which the analogous normal tissues were unstained, including cells of some fibrosarcomas, rhabdomyosarcomas, hemangiopericytomas and proliferating myoepithelial cells in mixed mammary tumors. Although PNA binding is complex and heterogeneous in canine tissues and does not appear to immunohistochemically detect a moiety associated with neoplastic transformation per se in the majority of canine tumors, the expression of PNA receptors may be associated with neoplastic changes in some mesenchymal cell populations.

Immunolocalization of aquaporin-8 in rat kidney, gastrointestinal tract, testis, and airways

2001 ◽  
Vol 281 (6) ◽  
pp. F1047-F1057 ◽  
Author(s):  
Marie-Louise Elkjær ◽  
Lene N. Nejsum ◽  
Veronika Gresz ◽  
Tae-Hwan Kwon ◽  
Uffe B. Jensen ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Southern Blotting ◽  
Rat Kidney ◽  
Cell Types ◽  
Myoepithelial Cells ◽  
Proximal Tubules ◽  
Basal Cells ◽  
Rt Pcr ◽  
Collecting Ducts ◽  
Outer Stripe

First published August 8, 2001; 10.1152/ajprenal.00158.2001.—The purpose of this study was to determine the cellular and subcellular localization of aquaporin-8 (AQP8) in rat kidney and other organs by RT-PCR analyses and by immunoblotting and immunohistochemistry using peptide-derived rabbit antibodies to rat AQP8. RT-PCR and Southern blotting revealed the presence of AQP8 mRNA in all kidney zones. LLC-PK1 cells transfected with a rat AQP8 construct exhibited strong labeling with the affinity-purified antibodies, whereas controls using cells transfected with the vector, but without the insert, were negative. The labeling was almost exclusively associated with intracellular vesicles. Immunoblotting of kidney membrane fractions revealed a predominant single band of 26–28 kDa. AQP8 immunoreactivity was mainly present in the cortex and outer stripe of the outer medulla. Sequential ultracentrifugation of rat kidney membrane revealed that AQP8 resides predominantly in intracellular vesicular fractions. Immunocytochemistry revealed modest labeling of proximal tubules and weak labeling of collecting ducts in cortex and medulla of rat kidney. The labeling was confined to cytoplasmic areas with no labeling of the brush border. Immunoblotting and RT-PCR/Southern blotting also revealed the presence of AQP8 protein and mRNA in rat liver, testis, epididymis, duodenum, jejunum, colon, and bronchi/trachea. Consistent with this, immunohistochemistry revealed AQP8 labeling in the hepatocytes and spematogenic cells in testis and in the basal cells in ductus epididymis, trachea, and bronchial epithelia. Moreover, AQP8 labeling was observed in the myoepithelial cells in salivary, bronchial, and tracheal glands with no labeling of acini or ductal epithelial cells. AQP8 is also present in the surface epithelial cells in duodenum, jejunum, and colon. In conclusion, AQP8 is expressed at low levels in rat kidney proximal tubules and collecting ducts, and it is present in distinct cell types in liver, testis, epididymis, duodenum, jejunum, colon, trachea, and principal bronchi as well as in multiple glands, including salivary glands.

scholarly journals p63 Is Expressed in Basal and Myoepithelial Cells of Human Normal and Tumor Salivary Gland Tissues

2003 ◽  
Vol 51 (2) ◽  
pp. 133-139 ◽  
Author(s):  
Hadi Bilal ◽  
Adriana Handra-Luca ◽  
Jacques-Charles Bertrand ◽  
Pierre J. Fouret
Keyword(s):  
Salivary Gland ◽  
Myoepithelial Cells ◽  
Salivary Gland Tumors ◽  
Basal Cells ◽  
Squamous Cells ◽  
Human Salivary Gland ◽  
Duct Cells ◽  
Normal Human ◽  
Luminal Cells ◽  
Tumor Types

p63 is essential for epithelial cell survival and may function as an oncogene. We examined by immunohistochemistry p63 expression in human normal and tumor salivary gland tissues. In normal salivary glands, p63 was expressed in the nuclei of myoepithelial and basal duct cells. Among 68 representative salivary gland tumors, 63 displayed p63 reactivity. In all tumor types differentiated towards luminal and myoepithelial lineages (pleomorphic adenomas, basal cell adenomas, adenoid cystic carcinomas, and epithelial-myoepithelial carcinomas), p63 was expressed in myoepithelial cells, whereas luminal cells were always negative. Similarly, in mucoepidermoid carcinomas, basal, intermediate, and squamous cells expressed p63, in contrast to luminal mucous cells. p63 reactivity was also restricted to basal cells in Warthin tumors and oncocytomas. Myoepitheliomas and myoepithelial carcinomas all expressed p63. The only five negative tumors were three of four acinar cell carcinomas and two of three adenocarcinomas. In conclusion, p63 is expressed in the nuclei of normal human salivary gland myoepithelial and basal duct cells. p63 expression is retained in the modified myoepithelial and basal cells of human salivary gland tumors, which suggests a role for p63 in oncogenesis of these complex tumors.

scholarly journals Luminal MCF-12A and myoepithelial-like Hs 578Bst cells form bilayered acini similar to human breast

2018 ◽  
Author(s):  
Anne Weber-Ouellette ◽  
Mélanie Busby ◽  
Isabelle Plante
Keyword(s):  
Cell Lines ◽  
Smooth Muscle Actin ◽  
Three Dimensional ◽  
Myoepithelial Cells ◽  
Normal Breast ◽  
Breast Development ◽  
Basal Cells ◽  
Culture Model ◽  
Luminal And Myoepithelial Cells

2.3.1AbstractThe mammary gland is a complex organ, structured in a ramified epithelium supported by the stroma. The epithelium’s functional unit is the bilayered acinus, made of a layer of luminal cells surrounded by a layer of basal cells mainly composed of myoepithelial cells. The aim of this study was to develop a reproducible and manipulable three-dimensional co-culture model of the bilayered acinus in vitro to study the interactions between the two layers. Two different combinations of cell lines were co-cultured in Matrigel: SCp2 and SCg6 mice cells, or MCF-12A and Hs 578Bst human cell lines. Cell ratios and Matrigel concentration were optimized. The resulting acini were analysed by confocal microscopy using epithelial (E-cadherin) and myoepithelial (α-smooth muscle actin) markers. SCp2 and SCg6 cells formed distinct three-dimensional structures, whereas MCF-12A and Hs 578Bst cells formed some bilayered acini. This in vitro bilayered acini model will allow us to understand the role of interactions between luminal and myoepithelial cells in the normal breast development.

CD109, a new marker for myoepithelial cells of mammary, salivary, and lacrimal glands and prostate basal cells

2007 ◽  
Vol 57 (5) ◽  
pp. 245-250 ◽  
Author(s):  
Masaki Hasegawa ◽  
Sumitaka Hagiwara ◽  
Tomoko Sato ◽  
Mayumi Jijiwa ◽  
Yoshiki Murakumo ◽  
...  
Keyword(s):  
Myoepithelial Cells ◽  
Basal Cells ◽  
Lacrimal Glands
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