Desmogleins are desmosomal cadherins that mediate cell–cell adhesion. In stratified squamous epithelia there are two major isoforms of desmoglein, 1 and 3, with different distributions in epidermis and mucous membrane. Since either desmoglein isoform alone can mediate adhesion, the reason for their differential distribution is not known. To address this issue, we engineered transgenic mice with desmoglein 3 under the control of the involucrin promoter. These mice expressed desmoglein 3 with the same distribution in epidermis as found in normal oral mucous membranes, while expression of other major differentiation molecules was unchanged. Although the nucleated epidermis appeared normal, the epidermal stratum corneum was abnormal with gross scaling, and a lamellar histology resembling that of normal mucous membrane. The mice died shortly after birth with severe dehydration, suggesting excessive transepidermal water loss, which was confirmed by in vitro and in vivo measurement. Ultrastructure of the stratum corneum showed premature loss of cohesion of corneocytes. This dysadhesion of corneocytes and its contribution to increased transepidermal water loss was confirmed by tape stripping. These data demonstrate that differential expression of desmoglein isoforms affects the major function of epidermis, the permeability barrier, by altering the structure of the stratum corneum.
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16 April 2001
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April 09 2001
Desmoglein Isoform Distribution Affects Stratum Corneum Structure and Function
Peter M. Elias,
Peter M. Elias
aDepartment of Dermatology, University of California San Francisco, San Francisco, California 94143
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Norihisa Matsuyoshi,
Norihisa Matsuyoshi
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
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Hong Wu,
Hong Wu
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
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Chenyan Lin,
Chenyan Lin
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
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Zhi Hong Wang,
Zhi Hong Wang
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
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Barbara E. Brown,
Barbara E. Brown
aDepartment of Dermatology, University of California San Francisco, San Francisco, California 94143
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John R. Stanley
John R. Stanley
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
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Peter M. Elias
aDepartment of Dermatology, University of California San Francisco, San Francisco, California 94143
Norihisa Matsuyoshi
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Hong Wu
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Chenyan Lin
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Zhi Hong Wang
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Barbara E. Brown
aDepartment of Dermatology, University of California San Francisco, San Francisco, California 94143
John R. Stanley
bDepartment of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Abbreviation used in this paper: Dsg, desmoglein.
Received:
December 01 2000
Revision Requested:
March 01 2001
Accepted:
March 01 2001
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Cell Biol (2001) 153 (2): 243–250.
Article history
Received:
December 01 2000
Revision Requested:
March 01 2001
Accepted:
March 01 2001
Citation
Peter M. Elias, Norihisa Matsuyoshi, Hong Wu, Chenyan Lin, Zhi Hong Wang, Barbara E. Brown, John R. Stanley; Desmoglein Isoform Distribution Affects Stratum Corneum Structure and Function. J Cell Biol 16 April 2001; 153 (2): 243–250. doi: https://doi.org/10.1083/jcb.153.2.243
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