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==Blistering diseases== ==Blistering diseases==
If the desmosomes connecting adjacent epithelial cells of the ] are not functioning correctly, layers of the skin can pull apart and allow abnormal movements of fluid within the skin, resulting in blisters and other tissue damage. Blistering diseases such as Pemphigus Vulgaris can be due to ] defects in desmosomal proteins or due to an ] response. These patients are often be found to have antibodies that bind to the desmosomal cadherins and disrupt the desmosomes. If the desmosomes connecting adjacent epithelial cells of the ] are not functioning correctly, layers of the skin can pull apart and allow abnormal movements of fluid within the skin, resulting in blisters and other tissue damage. Blistering diseases such as Pemphigus Vulgaris can be due to ] defects in desmosomal proteins or due to an ] response. These patients are often be found to have ] that bind to the desmosomal cadherins and disrupt the desmosomes.


==Hemidesmosomes == ==Hemidesmosomes ==

Revision as of 22:54, 18 March 2004

A Desmosome is a cell structure specialized for cell-to-cell adhesion. Desmosomes are molecular complexes of cell adhesion proteins and linking proteins that attach the cell surface adhesion proteins to intracellular keratin cytoskeletal filaments. The cell adhesion proteins of the desmosome are members of the cadherin family of cell adhesion molecules. They are transmembrane proteins that bridge the space between adjacent epithelial cells by way of homophilic binding of their extracellular domains to other desmosomal cadherins on the adjacent cell. The desmosomal linking proteins such as desmoplakin bind to the intracellular domain of cadherins and form a connecting bridge to the cytoskeleton.

cell adhesion in desmosomes

Blistering diseases

If the desmosomes connecting adjacent epithelial cells of the skin are not functioning correctly, layers of the skin can pull apart and allow abnormal movements of fluid within the skin, resulting in blisters and other tissue damage. Blistering diseases such as Pemphigus Vulgaris can be due to genetic defects in desmosomal proteins or due to an autoimmune response. These patients are often be found to have antibodies that bind to the desmosomal cadherins and disrupt the desmosomes.

Hemidesmosomes

When visualized by electron microscopy, hemidesmosomes are similar in appearance to desmosomes. Rather than linking two cells, hemidesmosomes attach one cell to the extracellular matrix. Rather than using cadherins, hemidesmosomes use integrin cell adhesion proteins.