In vitro, normal human keratinocytes reconstitute a differentiated stratified epidermis, maintaining the same gene expression pattern as its in vivo counterpart and are suitable for permanent grafting onto patients. Keratinocyte adhesion to basal lamina and lateral interactions among basal epidermal cells are also mediated by integrin receptors that are sorted to defined plasma membrane domains. The hemidesmosome-associated integrin α6β4 is sharply localized at the basal surface of basal cells and codistributes with laminin and nicein/kalinin; the α2β1 and α3β1 integrins are enriched laterally and play crucial roles in cell-cell interaction and proper colony morphology. During wound healing, proliferating and migrating keratinocytes express on their plasma membrane α(v)β5 and α5β1, which allow keratinocyte attachment and migration over the provisional matrix present in the wound. TGFβ, which is an autocrine and paracrine mediator in wound healing, specifically increases the synthesis and expression of α(v)β5 and α5β1, induces the de novo expression of α(v)β6, and determines the loss of integrin polarization. In hyperproliferative skin diseases, such as skin cancer or psoriasis vulgaris, and in normal keratinocytes forced into more frequent cell cycles, the polarized expression of integrins is lost, and α5β1 becomes costitutively expressed on the plasma membrane. In addition, the α6β4 integrin becomes associated with focal contacts. Nerve growth factor (NGF) is a potent autocrine stimulator of keratinocyte growth and induces melanocyte migration toward the leading edge of a healing wound. We are currently investigating the NGF-dependent modulation of integrin expression and function in keratinocytes and melanocytes in both normal epidermis and several hyperproliferative skin diseases.
|Number of pages||8|
|Journal||Journal of Dermatology|
|Publication status||Published - 1994|
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