Dermatopathological studies on skin lesions of MRL mice

F Furukawa, H Tanaka, K Sekita, T Nakamura… - Archives of …, 1984 - Springer
F Furukawa, H Tanaka, K Sekita, T Nakamura, Y Horiguchi, Y Hamashima
Archives of dermatological research, 1984Springer
The MRL-lpr/lpr (MRL/l) mouse is a new animal model for human systemic lupus
erythematosus (SLE) and skin lesions with hair loss and scab formation are one of the
characteristic manifestations in this mouse. We investigated the histopathology of the skin
lesions in MRL/l mice and studied the related autoimmune phenomenon. Light
microscopical observations revealed hyperkeratosis, acanthosis, hypergranulosis,
liquefaction, vasodilation in the dermis and T-cell infiltration into the dermis at the age of 5 …
Summary
The MRL-lpr/lpr(MRL/l) mouse is a new animal model for human systemic lupus erythematosus (SLE) and skin lesions with hair loss and scab formation are one of the characteristic manifestations in this mouse. We investigated the histopathology of the skin lesions in MRL/l mice and studied the related autoimmune phenomenon. Light microscopical observations revealed hyperkeratosis, acanthosis, hypergranulosis, liquefaction, vasodilation in the dermis and T-cell infiltration into the dermis at the age of 5 months (mo). Immunohistological studies showed the presence of immunoglobulins and/or complement depositions at the dermal-epidermal junction (DEJ). In some mice there was deposition of immunoglobulin at the DEJ at 2 mo and in 90%–100% of MRL/l mice at over 5 mo. Temporal relationship was present among cutaneous immunoglobulin depositions, the occurrence of anti-DNA antibodies and proteinuria. These findings suggest that MRL/l mice might provide a new aid for studying the biological mechanisms of the development of skin lesions in human SLE.
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