Characterization of Endothelin Release from Guinea-pig Tracheal Epithelium: Influence of Proinflammatory Mediators Including Major Basic Protein

1997 ◽  
Vol 10 (4) ◽  
pp. 189-198 ◽  
Author(s):  
D.W.P. Hay ◽  
M.R. Van Scott ◽  
R.M. Muccitelli
1979 ◽  
Vol 16 (9) ◽  
pp. 711-719 ◽  
Author(s):  
Donald L. Wassom ◽  
David A. Loegering ◽  
Gerald J. Gleich

2000 ◽  
Vol 67 (4) ◽  
pp. 567-576 ◽  
Author(s):  
MiMi P. Macias ◽  
Kenneth C. Welch ◽  
Karen L. Denzler ◽  
Kirsten A. Larson ◽  
Nancy A. Lee ◽  
...  

FEBS Letters ◽  
1991 ◽  
Vol 279 (2) ◽  
pp. 330-334 ◽  
Author(s):  
Ikuo Aoki ◽  
Yutaka Shindoh ◽  
Tsutomu Nishida ◽  
Satoru Nakai ◽  
Yeong-Man Hong ◽  
...  

1983 ◽  
Vol 158 (4) ◽  
pp. 1211-1226 ◽  
Author(s):  
D E Maddox ◽  
J H Butterfield ◽  
S J Ackerman ◽  
C B Coulam ◽  
G J Gleich

We have shown that serum levels of a molecule immunochemically similar to eosinophil granule major basic protein (MBP) are elevated in pregnant women throughout gestation. MBP levels increase during gestation and plateau at approximately 7,500 ng/ml by the 20th wk (greater than 10-fold above normal). Levels return to normal after delivery, with a T1/2 of 13.7 d. The MBP in pregnancy serum is remarkably similar to the eosinophil granule MBP in that: (a) pregnancy MBP fully inhibits the binding of radiolabeled MBP standard in a double antibody radioimmunoassay; (b) this inhibition reaction is specific for human MBP because pregnancy serum produces no inhibition of the binding of radiolabeled guinea pig MBP in the guinea pig MBP radioimmunoassay; (c) in a two-site immunoradiometric assay for MBP, slopes of dose-response curves for pregnancy serum, purified MBP, and serum from a patient with hypereosinophilic syndrome are identical, and maximal binding is comparable; (d) reduction and alkylation of pregnancy sera increases measured MBP 100-fold, as previously shown for eosinophil granule MBP in serum; and (e) the MBP in pregnancy serum demonstrates the same pattern of heat lability as has been previously reported for MBP. Four observations have raised the possibility that the eosinophil is not the source of the MBP in pregnancy serum: (a) no correlation between serum MBP level and peripheral blood eosinophil count exists in pregnant women, in contrast to previous studies of patients with eosinophilia; (b) levels of three other eosinophil-associated proteins are normal or low in pregnancy sera, whereas the serum levels of these proteins are elevated in patients with eosinophilia; (c) the slopes of dose-response curves for pregnancy sera and MBP standards differ in the double antibody radioimmunoassay; and (d) the molecule in pregnancy serum elutes from Sephadex G-50 columns at the void volume, while eosinophil granule MBP and the MBP in serum of patients with eosinophilia elute at a volume consistent with the previously established molecular weight of 9,300. These findings suggest that the MBP in pregnancy serum is derived from a source other than the eosinophil.


1978 ◽  
Vol 77 (3) ◽  
pp. 702-713 ◽  
Author(s):  
DM Lewis ◽  
JC Lewis ◽  
DA Loegering ◽  
GJ Gleich

The localization of the guinea pig eosinophil major basic protein (MBP) within the cell was investigated by the use of immunoelectron microscopy and by isolation of the granule crystalloids. First, by immunoperoxidase electron microscopy, we found that the MBP of eosinophil granules is contained within the crystalloid core of the granule. Specific staining of cores was present when rabbit antiserum to MBP was used as the first stage antibody in a double antibody staining procedure, whereas staining was not seen when normal rabbit serum was used as the first stage antibody. Second, crystalloids were isolated from eosinophil granules by disruption in 0.1% Triton X-100 and centrifugation through a cushion of 50% sucrose. Highly purified core preparations yielded essentially a single band when analyzed by electrophoresis on polyacrylamide gels containing 1% sodium dodecyl sulfate (SDS). The E1%1cm of the core protein was 26.8 +/- 1.0 (X +/- SEM); the E1%1cm for the MBP was 26.3. The core protein could not be distinguished from the MBP by radioimmunoassay (RIA) and essentially all of the protein in the core preparations could be accounted for as MBP. The results indicate that the MBP is contained in the core of the guinea pig eosinophil granule and that it is probably the only protein present in the core.


1976 ◽  
Vol 13 (9) ◽  
pp. 743-746 ◽  
Author(s):  
Daniel M. Lewis ◽  
David A. Loegering ◽  
Gerald J. Gleich

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