Carboxyamidotriazole (CAI) inhibits the adhesion of endometrial cancer cells to the basement membrane protein, laminin

1998 ◽  
Vol 5 (1) ◽  
pp. 80A-80A
Author(s):  
D ELMOWAFI ◽  
A MUNKARAH ◽  
R MORRIS ◽  
E KOHN ◽  
M DIAMOND ◽  
...  
1996 ◽  
Vol 270 (6) ◽  
pp. C1743-C1750 ◽  
Author(s):  
G. W. Laurie ◽  
J. D. Glass ◽  
R. A. Ogle ◽  
C. M. Stone ◽  
J. R. Sluss ◽  
...  

Regulated secretion requires the developmental coupling of neuronal or hormonal stimuli to an exocytotic response, a multistep pathway whose appearance may be linked with cellular adhesion to the newly formed exocrine cell basement membrane. We screened for adhesion-associated coupling activity using lacrimal acinar cells and have identified “BM180”, a novel basement membrane protein enriched in guanidine HCl extracts of lacrimal and parotid exocrine secretory glands. BM180 resides primarily in a previously inexamined lower molecular-mass basement membrane peak (peak 2) that contains cell adhesion activity inhibitable with the anti-BM180 monoclonal antibody 3E12. Removal of peak 2 by gel filtration or preincubation of basement membrane with 3E12 decreased regulated peroxidase secretion by one-half without affecting constitutive secretion or the amount of cellular peroxidase available for release. Adding back peak 2 restored regulated secretion in a dose-dependent and 3E12-inhibitable manner and suggested a synergistic relationship between BM180 and laminin 1. BM180 has a mobility of 180 and 60 kDa in the absence or presence of dithiothreitol, respectively, and shows no immunological identity by competitive enzyme-linked immunosorbent assay with laminin 1, collagen IV, entactin, fibronectin, BM-40, perlecan, or vitronectin. We propose that BM180 is an important resident of certain glandular basement membranes where it interacts with the cell surface, thereby possibly signaling the appearance of a transducing element in the stimulus-secretion coupling pathway.


FEBS Letters ◽  
1988 ◽  
Vol 236 (2) ◽  
pp. 352-356 ◽  
Author(s):  
Brigitte Lankat-Buttgereit ◽  
Karlheinz Mann ◽  
Rainer Deutzmann ◽  
Rupert Timpl ◽  
Thomas Krieg

2008 ◽  
Vol 1096 ◽  
Author(s):  
Hiroshi Horiguchi ◽  
Yoshitake Akiyama ◽  
Keisuke Morishima

AbstractWe have proposed a novel use of pulsating living cells as a driving source for a micro bio-actuator. Cardiyomyocytes contract autonomously using chemical energy. But, contractile force of a single cardiomyocyte is not enough to actuate a micro robot or a mechanical system. So it is necessary to reconstruct cardiomyocytes to increase the ability to contract. We focused on the reconstruction of cardiomyocytes using a basement membrane protein mixture. In this paper, we fabricated a prototype cardiomyocyte gel structure. We confirmed that the ring-shaped cardiomyocyte gel structure condensed around the central cylinder within the PDMS mold and contracted synchronously and autonomously.


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