4.3 Article

Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice

Journal

IMMUNOGENETICS
Volume 60, Issue 10, Pages 599-607

Publisher

SPRINGER
DOI: 10.1007/s00251-008-0320-4

Keywords

mast cell; lupus-prone mouse; hypotrichosis; desmoglein 4; early transposon

Funding

  1. Ministry of Education, Science, Sports, and Culture of Japan [16790221, 16390113, 19390108, 19659096]
  2. Grants-in-Aid for Scientific Research [19659096, 16790221, 19390108, 16390113] Funding Source: KAKEN

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Desmosomal cadherins are essential cell adhesion molecules expressed in the epidermis. We identified a mutation of a cadherin superfamily member, namely, desmoglein 4 (Dsg4), in early onset of death (EOD)(hage) mice with hypotrichosis. The mutation was induced by the insertion of an early transposon II-beta into intron 8 of Dsg4. Mast cell hyperplasia was observed in the skin of EOD(hage) mice. The abnormally expanded population of lpr T cells, i.e., CD4(-)CD8(-)B220(+)Thy1.2(+) alpha beta T cells, in the splenocytes of EOD mice was reduced in EOD(hage) mice. Therefore, it was suspected that the long-living mutant EOD(hage) mice were selected from lupus-prone EOD mice because of their immunological immaturity. These findings clearly indicate that Dsg4 is an important molecule for the formation of hair follicles and hypothesize that unorganized hyperplastic hair follicles in anagen due to the Dsg4 mutation provide niches for mast cell precursors in the skin.

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