Slow-Release Plastic Pellets (Elvax) for Localized In Situ Treatments of Mouse and Rat Mammary Tissue

Author(s):  
Gary B. Silberstein ◽  
Charles W. Daniel
Development ◽  
1991 ◽  
Vol 113 (3) ◽  
pp. 867-878 ◽  
Author(s):  
S.D. Robinson ◽  
G.B. Silberstein ◽  
A.B. Roberts ◽  
K.C. Flanders ◽  
C.W. Daniel

Transforming Growth Factor-beta 1 (TGF-beta 1) was previously shown to inhibit reversibly the growth of mouse mammary ducts when administered in vivo by miniature slow-release plastic implants. We now report a comparative analysis of three TGF-beta isoforms with respect to gene expression and localization of protein products within the mouse mammary gland. Our studies revealed overlapping expression patterns of TGF-beta 1, TGF-beta 2 and TGF-beta 3 within the epithelium of the actively-growing mammary end buds during branching morphogenesis, as well as within the epithelium of growth-quiescent ducts. However, TGF-beta 3 was the only isoform detected in myoepithelial progenitor cells (cap cells) of the growing end buds and myoepithelial cells of the mature ducts. During pregnancy, TGF-beta 2 and TGF-beta 3 transcripts increased to high levels, in contrast to TGF-beta 1 transcripts which were moderately abundant; TGF-beta 2 was significantly transcribed only during pregnancy. Molecular hybridization in situ revealed overlapping patterns of expression for the three TGF-beta isoforms during alveolar morphogenesis, but showed that, in contrast to the patterns of TGF-beta 1 and TGF-beta 2 expression, TGF-beta 3 is expressed more heavily in ducts than in alveoli during pregnancy. Developing alveolar tissue and its associated ducts displayed striking TGF-beta 3 immunoreactivity which was greatly reduced during lactation. All three isoforms showed dramatically reduced expression in lactating tissue. The biological effects of active, exogenous TGF-beta 2 and TGF-beta 3 were tested with slow-release plastic implants. These isoforms, like TGF-beta 1, inhibited mammary ductal elongation in situ by causing the disappearance of the proliferating stem cell layer (cap cells) and rapid involution of ductal end buds. None of the isoforms were active in inhibiting alveolar morphogenesis. We conclude that under the limited conditions of these tests, the three mammalian isoforms are functionally equivalent. However, striking differences in patterns of gene expression and in the distribution of immunoreactive peptides suggest that TGF-beta isoforms may have distinct roles in mammary growth regulation, morphogenesis and functional differentiation.


2014 ◽  
Vol 31 (4) ◽  
pp. 377-382 ◽  
Author(s):  
Massimiliano Baric ◽  
Lucia Pierro ◽  
Biancamaria Pietrangeli ◽  
Marco Petrangeli Papini

1986 ◽  
Vol 34 (7) ◽  
pp. 869-881 ◽  
Author(s):  
R B Nagle ◽  
W Böcker ◽  
J R Davis ◽  
H W Heid ◽  
M Kaufmann ◽  
...  

Two monoclonal antibodies, KA 1 and KA 4, raised against human epidermis, were biochemically and immunologically characterized and were shown to react with specific cytokeratin polypeptides. On frozen sections of human mammary gland, these antibodies distinguish between myoepithelial and luminal epithelial cells. We present evidence that in these cells KA 1 antibody recognized cytokeratin 5 and KA 4 antibody cytokeratin 19. In normal mammary tissue, KA 4 antibody invariably reacted with the epithelial cells lining the lumina of acini, ductules, ducts, and sinus. In contrast, KA 1 antibody decorated only the myoepithelial and basal epithelial cells of acini, ducts, and sinus. In ductules, however, KA 1 also stained the luminal cells. All 73 invasive lobular and ductal carcinomas studied reacted with KA 4 antibody; five of these were also positive, apparently in the same tumor cells, with KA 1. The tumor cells of in situ carcinomas were also stained in a homogeneous pattern with KA 4 antibody; KA 1 antibody reacted only with the surrounding myoepithelium. In epithelial hyperplasias, the proliferating cells were decorated by KA 1 and KA 4 antibodies in a heterogeneous pattern. Other antibodies were used for comparison. The results are discussed with respect to epithelial differentiation and pathogenesis and to the application of such antibodies for immunohistodiagnosis of mammary lesions.


1988 ◽  
Vol 68 (3) ◽  
pp. 779-786 ◽  
Author(s):  
P. H. ROBINSON ◽  
J. J. KENNELLY

High-moisture barley (HMB) was ensiled in polyethylene silage bags. Treatments applied to 30% moisture HMB as a percentage of dry matter (DM) were: none, 1% ammonia, 2% ammonia, and 1.5% sulphur dioxide. A fifth treatment was the addition of 1.5% sulphur dioxide to 20% moisture HMB. Barley samples were ruminally incubated to estimate degradability of DM and nitrogen (N). Ruminally incubated bags were also introduced to the duodenal cannulae and collected in feces to estimate true whole-tract digestion. Sulphur dioxide treatment, or moisture content, had no influence on ruminal degradability, with the exception of increased degradation rate of potentially degradable N for 20 vs 30% HMB, or whole-tract true digestion. Ammoniation resulted in net reduction in rate of ruminal DM release due to shift of soluble DM to the potentially degradable fraction, and decrease in the potentially degradable fraction degradation rate. Ammoniation increased barley N content up to 44% with no change in rate of ruminal N release. Whole-tract true DM digestion was higher for ammoniated barley but N digestion was not influenced. Sulphur dioxide appears to offer no advantages beyond grain preservation, whereas ammoniation offers potential by reducting rate of ruminal DM release, and providing a source of slow release nonprotein N, without affecting post-ruminal digestibility. Key words: High-moisture barley, ammonia, sulphur dioxide


1998 ◽  
Vol 65 (2) ◽  
pp. 199-208 ◽  
Author(s):  
DAVID T. CALVERT ◽  
TAE-GYU KIM ◽  
JAI-JUN CHOUNG ◽  
CAROLYNN BURNS ◽  
DAVID B. SHENNAN

The transport of L-glutamine by the lactating rat mammary gland has been investigated using rat mammary tissue explants and the in situ perfused rat mammary gland. L-glutamine uptake by both explants and the perfused mammary gland was via both Na+-dependent and Na+-independent pathways. It appeared that these pathways are situated on the blood-facing aspect of the mammary gland. L-glutamine uptake by both mammary preparations was markedly inhibited by 2-aminobicyclo[2,2,1]heptane-2-carboxylic acid in the absence of external Na+. This is consistent with L-glutamine uptake via system L. The Na+-dependent component(s) of L-glutamine uptake remains to be precisely identified. However, system A can be ruled out on the basis that L-glutamine was not inhibited by (methylamino)isobutyric acid. Mammary tissue concentrates L-glutamine with respect to both milk and plasma: we suggest that the Na+-dependent component(s) of L-glutamine uptake is responsible for generating the intracellular to extracellular concentration gradient.


2000 ◽  
Vol 166 (3) ◽  
pp. 503-510 ◽  
Author(s):  
F Sinowatz ◽  
D Schams ◽  
S Kolle ◽  
A Plath ◽  
D Lincoln ◽  
...  

We have used immunohistochemistry and non-radioactive in situ hybridisation to localise the GH receptor and its transcript in the bovine mammary gland during mammogenesis, lactation and involution. We found a characteristic pattern of immunoreactive GH (irGH) receptor distribution in the epithelial and stromal compartments during the different stages of mammary gland development: The ductular epithelium showed a distinct staining for irGH receptor during most stages, whereas the alveolar epithelium contained a modest amount of GH receptor during pregnancy which increased during lactation and galactopoiesis. In dry cows, the immunostaining for GH receptors in the alveolar epithelium was very weak or negative. Curiously, the amount of GH receptor mRNA appeared relatively constant during mammogenesis and lactation. The epithelial cells of the alveoli and ducts as well as the endothelial cells showed a distinct signal in our in situ hy! bridisation studies. The predominant localisation of GH receptors in the epithelium of ducts and alveoli is supportive of a role for GH in epithelial differentiation and maintenance. Furthermore, the increased intensity of immunostaining in bovine mammary tissue post partum suggests a direct role for GH receptor in mediating the effect of GH in milk production and secretion.


2019 ◽  
Vol 8 (5) ◽  
pp. 1970016
Author(s):  
Arjyabaran Sinha ◽  
Youngjin Choi ◽  
Minh Hoang Nguyen ◽  
Thanh Loc Nguyen ◽  
Seung Woo Choi ◽  
...  
Keyword(s):  

Chemosphere ◽  
2019 ◽  
Vol 221 ◽  
pp. 802-811 ◽  
Author(s):  
Patrick J. Evans ◽  
Pamela Dugan ◽  
Dung Nguyen ◽  
Michael Lamar ◽  
Michelle Crimi

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