ADAM33 Expression in Asthmatic Airways and Human Embryonic Lungs

2005 ◽  
Vol 171 (9) ◽  
pp. 958-965 ◽  
Author(s):  
Hans Michael Haitchi ◽  
Robert M. Powell ◽  
Timothy J. Shaw ◽  
Peter H. Howarth ◽  
Susan J. Wilson ◽  
...  
Keyword(s):  
Development ◽  
1996 ◽  
Vol 122 (6) ◽  
pp. 1759-1767 ◽  
Author(s):  
L. Schuger ◽  
G.R. Johnson ◽  
K. Gilbride ◽  
G.D. Plowman ◽  
R. Mandel

Epithelial and mesenchymal cells isolated from mouse embryonic lungs synthesized and responded to amphiregulin (AR) in a different fashion. Mesenchymal cells produced and deposited 3- to 4-fold more AR than epithelial cells, proliferated in the presence of exogenous AR, and their spontaneous growth was blocked by up to 85% by anti-AR antibodies. In contrast, epithelial cells exhibited a broad response to this growth regulator factor depending on whether they were supplemented with extracellular matrix (ECM) and whether this ECM was of epithelial or mesenchymal origin. AR-treated epithelial cells proliferated by up to 3-fold in the presence of mesenchymal-deposited ECM, remained unchanged in the presence of epithelial-deposited ECM, and decreased in their proliferation rate below controls in the absence of ECM supplementation. This effect was abolished by treatment with the glycosaminoglycan-degrading enzymes heparinase and heparitinase suggesting the specific involvement of heparan sulfate proteoglycan (HSPG) in AR-mediated cell proliferation. In whole lung explants, branching morphogenesis was inhibited by antibodies against the AR heparan sulfate binding site and stimulated by exogenous AR. Since during development, epithelial cells are in contact with mesenchymal ECM at the tips of the growing buds and alongside the basement membrane, focal variations in the proportion of epithelial and mesenchymal HSPG will focally affect epithelial proliferation rates. Therefore, AR-HSPG interaction may underlie the process of branching morphogenesis by inducing differential cell proliferation.


2014 ◽  
Vol 306 (1) ◽  
pp. L10-L22 ◽  
Author(s):  
Yan Cai ◽  
Melissa E. Winn ◽  
John K. Zehmer ◽  
William K. Gillette ◽  
Jacek T. Lubkowski ◽  
...  

Secretoglobin (SCGB) 3A2 is a member of the SCGB gene superfamily of small secreted proteins, predominantly expressed in lung airways. We hypothesize that human SCGB3A2 may exhibit anti-inflammatory, growth factor, and antifibrotic activities and be of clinical utility. Recombinant human SCGB3A2 was expressed, purified, and biochemically characterized as a first step to its development as a therapeutic agent in clinical settings. Human SCGB3A2, as well as mouse SCGB3A2, readily formed a dimer in solution and exhibited novel phospholipase A2 inhibitory activity. This is the first demonstration of any quantitative biochemical measurement for the evaluation of SCGB3A2 protein. In the mouse as an experimental animal, human SCGB3A2 exhibited growth factor activity by promoting embryonic lung development in both ex vivo and in vivo systems and antifibrotic activity in the bleomycin-induced lung fibrosis model. The results suggested that human SCGB3A2 can function as a growth factor and an antifibrotic agent in humans. When SCGB3A2 was administered to pregnant female mice through the tail vein, the protein was detected in the dam's serum and lung, as well as the placenta, amniotic fluids, and embryonic lungs at 10 min postadministration, suggesting that SCGB3A2 readily crosses the placenta. The results warrant further development of recombinant SCGB3A2 as a therapeutic agent in treating patients suffering from lung diseases or preterm infants with respiratory distress.


1997 ◽  
Vol 60 (1) ◽  
pp. 38-48 ◽  
Author(s):  
Heber C. Nielsen ◽  
Ana Martin ◽  
MaryAnn V. Volpe ◽  
Dimitrios Hatzis ◽  
Robert J. Vosatka

2015 ◽  
Vol 5 (2) ◽  
pp. 382-397 ◽  
Author(s):  
Kaori Ihida-Stansbury ◽  
Juliana Ames ◽  
Mithil Chokshi ◽  
Norman Aiad ◽  
Sonali Sanyal ◽  
...  

2010 ◽  
Vol 27 (2) ◽  
pp. 181-185 ◽  
Author(s):  
Toko Shinkai ◽  
Masato Shinkai ◽  
Martina A. Pirker ◽  
Sandra Montedonico ◽  
Prem Puri

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