scholarly journals In vitroRelease of Eosinophil Proteins in Allergic and Atopic Dermatitis Patients

1994 ◽  
Vol 3 (3) ◽  
pp. 223-227 ◽  
Author(s):  
L. K. Poulsen ◽  
C. M. Reimert ◽  
C. Bindslev-Jensen

To investigate whether eosinophils are stimulatedin vivoor have acquired an increased susceptibility to stimuli from the coagulation cascade, the release of eosinophil proteins was compared for three groups of donors with different levels of serum IgE. (1) with atopic dermatitis (s-IgE > 5000 IU/ml,n= 11); (2) with inhalant allergy (200 < s-IgE < 2 000 IU/ml,n= 10); and (3) non-allergic (s- IgE < 100 IU/ml,n= 10). The levels of eosinophil cationic protein and eosinophil protein X (ECP, EPX) were determined in serum (clotting time = 2.0 h) and plasma. Serum and plasma ECP in normal donors demonstrated large intra-personal variations (C.V. 50–80%), but serum-ECP (mean 8.1 ng/ml) was clearly distinguishable from plasma ECP (mean 1.0 ng/ml) by a factor of 8 (range: 5.6–11.6). The ECP released during clotting was markedly increased in the atopic dermatitis group (serum:plasma ratio 13.5,p<0.003) compared with the other groups (6.7 and 5.6). EPX, having a higher plasma level, demonstrated a less pronounced release (serum: plasma ratios 2.0, 1.7 and 1.4), with no statistical difference between donor groups. Considering all donors together the levels of ECP and EPX in plasma and in serum were correlated to the number of eosinophils (coefficients of correlation 0.54-0.58,p<0.002).

Author(s):  
Kouichi Ikai ◽  
Atsuhiko Ogino ◽  
Ikuko Furukawa ◽  
Motoaki Ozaki ◽  
Mayumi Fujita ◽  
...  

1991 ◽  
Vol 96 (2) ◽  
pp. 175-178 ◽  
Author(s):  
R. Paganelli ◽  
E. Fanales-Belasio ◽  
D. Carmini ◽  
E. Scala ◽  
P. Meglio ◽  
...  

CHEST Journal ◽  
1993 ◽  
Vol 103 (2) ◽  
pp. 475-478 ◽  
Author(s):  
Tom Pettersson ◽  
Henrik Riska ◽  
Seppo Sutinen ◽  
Matti Klockars ◽  
Christer Peterson

2006 ◽  
Vol 45 (10) ◽  
pp. 1156-1160 ◽  
Author(s):  
Murat-Sušić Slobodna ◽  
Lipozenčić Jasna ◽  
Žiǎić Vesna ◽  
Husar Karmela ◽  
Marinović Branka

2015 ◽  
Vol 7 (284) ◽  
pp. 284ra60-284ra60 ◽  
Author(s):  
Polina L. Yarova ◽  
Alecia L. Stewart ◽  
Venkatachalem Sathish ◽  
Rodney D. Britt ◽  
Michael A. Thompson ◽  
...  

Airway hyperresponsiveness and inflammation are fundamental hallmarks of allergic asthma that are accompanied by increases in certain polycations, such as eosinophil cationic protein. Levels of these cations in body fluids correlate with asthma severity. We show that polycations and elevated extracellular calcium activate the human recombinant and native calcium-sensing receptor (CaSR), leading to intracellular calcium mobilization, cyclic adenosine monophosphate breakdown, and p38 mitogen-activated protein kinase phosphorylation in airway smooth muscle (ASM) cells. These effects can be prevented by CaSR antagonists, termed calcilytics. Moreover, asthmatic patients and allergen-sensitized mice expressed more CaSR in ASMs than did their healthy counterparts. Indeed, polycations induced hyperreactivity in mouse bronchi, and this effect was prevented by calcilytics and absent in mice with CaSR ablation from ASM. Calcilytics also reduced airway hyperresponsiveness and inflammation in allergen-sensitized mice in vivo. These data show that a functional CaSR is up-regulated in asthmatic ASM and targeted by locally produced polycations to induce hyperresponsiveness and inflammation. Thus, calcilytics may represent effective asthma therapeutics.


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