Acantholytic change of psoriatic‐involved epidermis during organ culture in vitro

Incubation of unfixed skin slices in RPMI 1640 medium for 24—48 h resulted in two types of histological change in psoriatic‐involved epidermis. The degenerative change was the major finding in 7 out of 11 psoriatic‐involved epidermis, whereas the acantholytic change was observed in the remaining four cases. Neither degenerative nor acantholytic changes were observed in psoriatic‐uninvolved epidermis (11 cases) or in normal human epidermis (5 cases). The acantholytic change was observed after only a 12‐h incubation and was significantly (but not completely) inhibited by the addition of soybean trypsin inhibitor, which had no effect on the degenerative change of keratinocytes. The addition of hydrocortisone in the incubation medium had no effect on cither degenerative or acantholytic changes of keratinocytes. Our results indicate that a significant population of psoriatic‐involved epidermis reveals acantholysis during organ culture in vitro, which might be, at least in part, induced by serine‐type protease, the activity of which is known to be increased in the psoriatic‐involved epidermis.

[1]  H. Iizuka,et al.  Effects of retinoids on the cyclic AMP system of pig skin epidermis. , 1985, The Journal of investigative dermatology.

[2]  J. Nakayama,et al.  STUDIES OF CELL AND ORGAN CULTURE OF PSORIATIC AND NORMAL EPIDERMIS IN VITRO , 1983, The Journal of dermatology.

[3]  J. Fraki,et al.  Correlation of epidermal plasminogen activator activity with disease activity in psoriasis , 1983, The British journal of dermatology.

[4]  K. Hashimoto,et al.  Anti-cell surface pemphigus autoantibody stimulates plasminogen activator activity of human epidermal cells. A mechanism for the loss of epidermal cohesion and blister formation , 1983, The Journal of experimental medicine.

[5]  L. Dubertret,et al.  Localization of proteolytic activity in psoriatic skin. , 1982, The British journal of dermatology.

[6]  H. Iizuka,et al.  Effects of trypsin on the cyclic AMP system of the pig skin. , 1981, The Journal of investigative dermatology.

[7]  H. Ogawa,et al.  The pathogenic role of pemphigus antibodies and proteinase in epidermal acantholysis. , 1981, The Journal of investigative dermatology.

[8]  H. Iizuka,et al.  Epinephrine-induced cyclic AMP accumulation in the psoriatic epidermis. , 1981, Acta dermato-venereologica.

[9]  S. Jabłońska,et al.  The activity of polymorphonuclear leukocyte neutral proteinases and their inhibitors in patients with psoriasis treated with a continuous peritoneal dialysis. , 1980, The Journal of investigative dermatology.

[10]  H. Iizuka,et al.  Cyclic AMP accumulation in psoriatic skin: differential responses to histamine, AMP, and einephrine by the uninvolved and involved epidermis. , 1978, The Journal of investigative dermatology.

[11]  K. Yoshikawa,et al.  Cyclic AMP and psoriasis. , 1975, The Journal of investigative dermatology.

[12]  H. Braunsteiner,et al.  Cationic proteins from human neutrophil granulocytes. Evidence for their chymotrypsin-like properties. , 1975, Biochimica et biophysica acta.

[13]  B. Flaxman,et al.  Organ culture of human skin in chemically defined medium. , 1975, The Journal of investigative dermatology.

[14]  G. Hambrick,et al.  The behavior of explants of psoriasis in vitro. , 1969, The Journal of investigative dermatology.

[15]  G. Caron Organ culture of normal and psoriatic skin. , 1968, Archives of dermatology.