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DOI 10.1111/j.1365-2133.1992.tb00454.x

Медицинская библиотека · The British journal of dermatology · 1992

A quantitative immunohistochemical study of the expression of integrins by nerves in psoriatic and normal skin.

Andrew S M, Edwards B D, Chalmers R J, O'Driscoll J B

Сравнительное исследованиеСтатьяПеревод в очереди

Аннотация

Qualitative and quantitative assessment of integrin expression by dermal nerves was made by an avidin-biotin immunoperoxidase method on snap-frozen biopsies from affected psoriatic skin, and skin from normal control subjects with no history of skin disease. Nerves expressed alpha 1, alpha 2, alpha 3, alpha 6, beta 1 and beta 4 integrin subunits, and perineural sheaths in the mid-dermis also expressed these subunits, with the exception of alpha 2. There were more upper dermal nerve segments expressing alpha 1 integrin compared with other integrins both in controls and in psoriatic skin. The greater number of nerves expressing alpha 1 integrin compared with other integrins may be due to anatomical or functional differences between groups of nerves. There were significantly more nerves expressing alpha 1, alpha 2, alpha 3, alpha 6 and beta 4 integrins in psoriatic skin compared with control skin. This generalized increase may indicate a secondary trophic effect on all nerves rather than a specific increase in one type of nerve. However, the expression of alpha 2 integrin may be significant in the pathogenesis of the psoriatic plaque, in that it was barely detectable in the normal site-matched biopsies, but much greater in psoriatic plaques. The study of the expression of adhesion molecules by neurones in psoriasis offers a new avenue for investigation of the role of neuronal hypertrophy in the initiation and maintenance of psoriatic plaques.

Для цитирования: Andrew S M, Edwards B D, Chalmers R J, O'Driscoll J B. A quantitative immunohistochemical study of the expression of integrins by nerves in psoriatic and normal skin.. The British journal of dermatology. 1992. DOI: 10.1111/j.1365-2133.1992.tb00454.x.

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