scholarly journals Down-regulation and Inactivation of Neutral Endopeptidase 24.11 (Enkephalinase) in Human Neutrophils

1989 ◽  
Vol 264 (24) ◽  
pp. 14519-14523
Author(s):  
E G Erdös ◽  
B Wagner ◽  
C B Harbury ◽  
R G Painter ◽  
R A Skidgel ◽  
...  
Author(s):  
V. Kriho ◽  
B. Wagner ◽  
E.G. Erdos ◽  
R.P. Becker

We have documented the presence of neutral endopeptidase 24.11 (NEP), on the surface of human neutrophils (PMN) and PMN cytoplasts. Cytoplasts are whole cell preparations which contain cytomatrix, but lack internal membranes and organelles ,such as nuclei and lysosomal granules. These structures have been extracted mechanically, leaving the plasma membrane “outside-out” topology intact. Cytoplasts are very useful in correlative studies of cell surface structure and function. Biochemically, the membrane component of cytoplasts is predominantly plasma membrane; structurally, chemical activity may be localized to domains of the intact cell surface. NEP is a membrane-bound metalloendopeptidase present in human PMN' s. We have marked NEP on the plasma membranes of PMNs and PMN cytoplasts via pre-embedding iramunocytochemistry. We used scanning electron microscopy (SEM) with backscattered electron imaging (BEI) to visualize Au labelled anti-NEP on the surface of a large number of cells. Transmission electron microscopy (TEM) was used to confirm the presence of the enzyme on PMN's and PMN cytoplasts.Suspensions of PMN or PMN cytoplasts (2 x 106 cells/ml) were fixed for 8 min at room temp. in 0.25% glutaraldehyde in phosphate buffered saline (PBS) pH 7.2 rinsed in PBS, treated with 0.1% glycine in PBS for 10 rain and then incubated for 15 min in 5% normal goat serum (NGS) in 0.1% bovine serum albumin dissolved in PBS (BSA/PBS). Following this step, cells were incubated for 20 min in anti- NEP antibody, rinsed in BSA/PBS, incubated in goat anti-rabbit IgG coupled to 15nm colloidal Au particles (GARG15) for 1 h and again rinsed in PBS. Postfixation for 30 min in 2.5% glutaraldehyde and PBS rinsing followed. For SEM a drop of cell suspension was put on a polylysine- treated Formvar-carbon-coated Au grid and cells were allowed to settle and attach for 30 min. The grid was rinsed in water, dehydrated and critical point dried. Cells were coated with carbon before viewing by SEM. For TEM, following immunolabelling, cells were post-fixed in OsO4, rinsed, dehydrated and embedded in Epon for sectioning.


1995 ◽  
Vol 89 (1) ◽  
pp. 83-89 ◽  
Author(s):  
Christine Fagny ◽  
Arnaud Marchant ◽  
Eric De Prez ◽  
Michel Goldman ◽  
Monique Deschodt-Lanckman

1. As lipopolysaccharide is a major stimulator of neutrophil responses during Gram-negative bacterial infections, we studied its effect on the membrane expression of neutral endopeptidase 24.11/CD10 on neutrophils in a model of endotoxaemia in vitro. Lipopolysaccharide added to human whole-blood induced a marked and sustained CD10/neutral endopeptidase upregulation that was already detectable at 0.1 ng/ml and was maximal at a lipopolysaccharide concentration of 10 ng/ml. 2. We observed that neither tumour necrosis factor-α nor any newly synthesized protein was involved in the upregulation observed after 1 h incubation with 10 ng/ml lipopolysaccharide. 3. We further studied whether the lipopolysaccharide-induced CD10/neutral endopeptidase upregulation was mediated by lipopolysaccharide binding to the neutrophil CD14 receptor. Incubation of whole blood with an anti-CD14 monoclonal antibody before the addition of 0.1 ng/ml or 0.5 ng/ml lipopolysaccharide resulted in complete inhibition of CD10/neutral endopeptidase upregulation. In contrast, at a lipopolysaccharide concentration of 10 ng/ml, the anti-CD14 monoclonal antibody had an incomplete blocking effect. 4. The differential requirement for the CD14 receptor, depending on the lipopolysaccharide dose, was confirmed by the study of a patient suffering from paroxysmal nocturnal haemoglobinuria (in whom a complete defect in neutrophil CD14 expression was previously documented). 5. We finally confirmed these results using purified neutrophils, demonstrating that lipopolysaccharide-induced CD10/neutral endopeptidase upregulation depends on direct interaction with neutrophil CD14.


1985 ◽  
Vol 82 (24) ◽  
pp. 8737-8741 ◽  
Author(s):  
J. C. Connelly ◽  
R. A. Skidgel ◽  
W. W. Schulz ◽  
A. R. Johnson ◽  
E. G. Erdos

1990 ◽  
Vol 265 (24) ◽  
pp. 14150-14155
Author(s):  
J. Vijayaraghavan ◽  
A.G. Scicli ◽  
O.A. Carretero ◽  
C. Slaughter ◽  
C. Moomaw ◽  
...  

1995 ◽  
Vol 5 (2) ◽  
pp. 151-154 ◽  
Author(s):  
Stéphane De Lombaer ◽  
Louis Blanchard ◽  
Carol Berry ◽  
Rajendra D. Ghai ◽  
Angelo J. Trapani

Blood ◽  
2003 ◽  
Vol 102 (8) ◽  
pp. 3028-3034 ◽  
Author(s):  
Soohee Lee ◽  
Asim K. Debnath ◽  
Colvin M. Redman

Abstract In addition to its importance in transfusion, Kell protein is a member of the M13 family of zinc endopeptidases and functions as an endothelin-3–converting enzyme. To obtain information on the structure of Kell protein we built a model based on the crystal structure of the ectodomain of neutral endopeptidase 24.11 (NEP). Similar to NEP, the Kell protein has 2 globular domains consisting mostly of α-helical segments. The domain situated closest to the membrane contains both the N- and C-terminal sequences and the enzyme-active site. The outer domain contains all of the amino acids whose substitutions lead to different Kell blood group phenotypes. In the model, the zinc peptidase inhibitor, phosphoramidon, was docked in the active site. Site-directed mutagenesis of amino acids in the active site was performed and the enzymatic activities of expressed mutant Kell proteins analyzed and compared with NEP. Our studies indicate that Kell and NEP use the same homologous amino acids in the coordination of zinc and in peptide hydrolysis. However, Kell uses different amino acids than NEP in substrate binding and appears to have more flexibility in the composition of amino acids allowed in the active site.


2003 ◽  
Vol 278 (26) ◽  
pp. 24181-24188 ◽  
Author(s):  
Karim Dib ◽  
Fredrik Melander ◽  
Lena Axelsson ◽  
Marie-Claire Dagher ◽  
Pontus Aspenström ◽  
...  

2006 ◽  
Vol 17 (1) ◽  
pp. 16-38 ◽  
Author(s):  
David S. Cohen ◽  
Cynthia A. Fink ◽  
Angelo J. Trapani ◽  
Randy L. Webb ◽  
Patricia A. Zane ◽  
...  

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