<p>(<b>A</b>) Human keratinocytes with assembled desmosomes were treated with NH or PV IgG for 3 hrs either in the absence or presence of 1 mM mβCD. Dsg3 was detected by live labeling with AK15 for 30 min on ice. Keratinocytes treated with PV IgG exhibit disrupted Dsg3 staining (surface clustering and linear array formation). mβCD treatment prevented both Dsg3 clustering and linear array formation in response to PV IgG. (<b>B</b>) mβCD treatment protected desmosomes against PV IgG-induced fragmentation. Means ± SEM (<i>n</i> = 4–8 monolayers per group); *p<0.05. Scale bar in A, 10 µm.</p
In the human autoimmune blistering disease pemphigus vulgaris (PV) pathogenic antibodies bind the de...
<p>(<b>A</b>) Two PV patient samples, PV IgGa (patient #3270) and PV IgGb (patient #7860) were ident...
Desmosomes provide intercellular adhesive strength required for integrity of epithelial and some non...
<p>(<b>A–C</b>) Desmoplakin (DP) localization is unchanged upon addition of NH IgG. (<b>D–I</b>) PV ...
<p>(<b>A–C</b>) Dsg3 colocalization with various membrane markers was analyzed using structured illu...
<p>(<b>A–H</b>) Cell surface Dsg3 was pulse-labeled with biotinylated AK23 and detected using strept...
<p>(<b>A–D</b>) Cell surface Dsg3 was labeled with biotin-conjugated AK23 monoclonal antibody follow...
Pemphigus vulgaris (PV) is an epidermal blistering disorder caused by antibodies directed against th...
Pemphigus vulgaris (PV) is a severe autoimmune disease in which autoantibodies against the desmosoma...
AbstractDefects of cell–cell adhesion underlie disruption of epithelial integrity observed in patien...
Pemphigus vulgaris (PV) is a potentially lethal autoimmune disease characterized by blister formatio...
The intercellular interactions of the desmosomal cadherins, desmoglein and desmocollin, are required...
<p>A) Immunofluorescence analysis to examine localization of various desmosomal components in <i>Dsg...
<div><p>Strong intercellular adhesion is critical for tissues that experience mechanical stress, suc...
<p>Pemphigus vulgaris (PV) is a potentially lethal autoimmune disease characterized by blister forma...
In the human autoimmune blistering disease pemphigus vulgaris (PV) pathogenic antibodies bind the de...
<p>(<b>A</b>) Two PV patient samples, PV IgGa (patient #3270) and PV IgGb (patient #7860) were ident...
Desmosomes provide intercellular adhesive strength required for integrity of epithelial and some non...
<p>(<b>A–C</b>) Desmoplakin (DP) localization is unchanged upon addition of NH IgG. (<b>D–I</b>) PV ...
<p>(<b>A–C</b>) Dsg3 colocalization with various membrane markers was analyzed using structured illu...
<p>(<b>A–H</b>) Cell surface Dsg3 was pulse-labeled with biotinylated AK23 and detected using strept...
<p>(<b>A–D</b>) Cell surface Dsg3 was labeled with biotin-conjugated AK23 monoclonal antibody follow...
Pemphigus vulgaris (PV) is an epidermal blistering disorder caused by antibodies directed against th...
Pemphigus vulgaris (PV) is a severe autoimmune disease in which autoantibodies against the desmosoma...
AbstractDefects of cell–cell adhesion underlie disruption of epithelial integrity observed in patien...
Pemphigus vulgaris (PV) is a potentially lethal autoimmune disease characterized by blister formatio...
The intercellular interactions of the desmosomal cadherins, desmoglein and desmocollin, are required...
<p>A) Immunofluorescence analysis to examine localization of various desmosomal components in <i>Dsg...
<div><p>Strong intercellular adhesion is critical for tissues that experience mechanical stress, suc...
<p>Pemphigus vulgaris (PV) is a potentially lethal autoimmune disease characterized by blister forma...
In the human autoimmune blistering disease pemphigus vulgaris (PV) pathogenic antibodies bind the de...
<p>(<b>A</b>) Two PV patient samples, PV IgGa (patient #3270) and PV IgGb (patient #7860) were ident...
Desmosomes provide intercellular adhesive strength required for integrity of epithelial and some non...