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Relationship of epidermal lipogenesis to cutaneous barrier function
Journal of Lipid Research
|June 1, 1987
Summary
Disrupting the skin barrier increases epidermal lipid and sterol synthesis. This response, crucial for barrier repair, appears regulated by water loss, not systemic factors.
Area of Science:
- Dermatology
- Biochemistry
- Skin Biology
Background:
- Mammalian stratum corneum lipids are vital for skin barrier function.
- Factors regulating epidermal lipid biosynthesis remain largely unknown.
- Previous research suggests barrier needs, not circulating sterols, control skin sterol synthesis.
Purpose of the Study:
- To investigate if barrier disruption globally stimulates epidermal lipogenesis.
- To identify the signaling mechanism behind lipid biosynthesis activation.
- To differentiate between epidermal and dermal lipid responses to barrier impairment.
Main Methods:
- Inducing skin barrier alterations using acetone, sodium dodecyl sulfate (SDS), and essential fatty acid deficiency (EFAD) in mice.
- Measuring epidermal and dermal sterol and fatty acid biosynthesis.
- Utilizing plastic occlusion to assess the role of water flux.
Main Results:
- Acetone and SDS treatments significantly increased epidermal sterol and fatty acid biosynthesis.
- Essential fatty acid deficiency (EFAD) also enhanced epidermal lipid synthesis.
- Plastic occlusion normalized lipid biosynthesis, suggesting water flux as a key signal.
Conclusions:
- Cutaneous permeability barrier disruption triggers a coordinated increase in epidermal sterol and fatty acid synthesis.
- This lipogenic stimulation is reversed upon barrier repair.
- Transcutaneous water gradients likely regulate epidermal lipogenesis.