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Research Article Free access | 10.1172/JCI118664

Expression of human group II PLA2 in transgenic mice results in epidermal hyperplasia in the absence of inflammatory infiltrate.

D S Grass, R H Felkner, M Y Chiang, R E Wallace, T J Nevalainen, C F Bennett, and M E Swanson

DNX Transgenics, Princeton, New Jersey 08540, USA.

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DNX Transgenics, Princeton, New Jersey 08540, USA.

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DNX Transgenics, Princeton, New Jersey 08540, USA.

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DNX Transgenics, Princeton, New Jersey 08540, USA.

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DNX Transgenics, Princeton, New Jersey 08540, USA.

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DNX Transgenics, Princeton, New Jersey 08540, USA.

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Published May 15, 1996 - More info

Published in Volume 97, Issue 10 on May 15, 1996
J Clin Invest. 1996;97(10):2233–2241. https://doi.org/10.1172/JCI118664.
© 1996 The American Society for Clinical Investigation
Published May 15, 1996 - Version history
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Abstract

Group II PLA2 has been implicated in inflammatory processes in both man and other animals and has been shown to be involved in inflammatory conditions, such as arthritis and sepsis. Transgenic mice expressing the human group II PLA2 gene have been generated using a 6.2-kb genomic fragment. These mice express the group II PLA2 gene abundantly in liver, lung, kidney, and skin, and have serum PLA2 activity levels approximately eightfold higher than nontransgenic littermates. The group II PLA2 transgenic mice reported here exhibit epidermal and adnexal hyperplasia, hyperkeratosis, and almost total alopecia. The chronic epidermal hyperplasia and hyperkeratosis seen in these mice is similar to that seen in a variety of dermatopathies, including psoriasis. However, unlike what is seen with these dermatopathies, no significant inflammatory-cell influx was observed in the skin of these animals, or in any other tissue examined. These mice provide an important tool for examining group II PLA2 expression, and for determining the role of group II PLA2 in normal and disease physiology. They serve as an in vivo model for identifying inhibitors of group II PLA2 activity and gene expression.

Version history
  • Version 1 (May 15, 1996): No description

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