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The stratum corneum: the rampart of the mammalian body
Author(s) -
Nishifuji Koji,
Yoon Ji Seon
Publication year - 2013
Publication title -
veterinary dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.744
H-Index - 60
eISSN - 1365-3164
pISSN - 0959-4493
DOI - 10.1111/j.1365-3164.2012.01090.x
Subject(s) - corneocyte , stratum corneum , loricrin , involucrin , desquamation , microbiology and biotechnology , filaggrin , chemistry , keratin , proteases , ichthyosis , epidermis (zoology) , biochemistry , ceramide , biophysics , keratinocyte , biology , atopic dermatitis , anatomy , dermatology , immunology , enzyme , genetics , medicine , apoptosis , in vitro
Background – The stratum corneum (SC) is the outermost region of the epidermis and plays key roles in cutaneous barrier function in mammals. The SC is composed of ‘bricks’, represented by flattened, protein‐enriched corneocytes, and ‘mortar’, represented by intercellular lipid‐enriched layers. As a result of this ‘bricks and mortar’ structure, the SC can be considered as a ‘rampart’ that encloses water and solutes essential for physiological homeostasis and that protects mammals from physical, chemical and biological assaults. Structures and functions – The corneocyte cytoskeleton contains tight bundles of keratin intermediate filaments aggregated with filaggrin monomers, which are subsequently degraded into natural moisturizing compounds by various proteases, including caspase 14. A cornified cell envelope is formed on the inner surface of the corneocyte plasma membrane by transglutaminase‐catalysed cross‐linking of involucrin and loricrin. Ceramides form a lipid envelope by covalently binding to the cornified cell envelope, and extracellular lamellar lipids play an important role in permeability barrier function. Corneodesmosomes are the main adhesive structures in the SC and are degraded by certain serine proteases, such as kallikreins, during desquamation. Clinical relevance – The roles of the different SC components, including the structural proteins in corneocytes, extracellular lipids and some proteins associated with lipid metabolism, have been investigated in genetically engineered mice and in naturally occurring hereditary skin diseases, such as ichthyosis, ichthyosis syndrome and atopic dermatitis in humans, cattle and dogs.