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Studies in cutaneous aging: II. The microvasculature
The Journal of Investigative Dermatology
|May 1, 1982
Summary
Sun exposure and aging impact skin microvessels differently. UV radiation and early aging thicken vessel walls via veil cells, while advanced aging thins them by reducing veil cell activity.
Area of Science:
- Dermatology
- Microcirculation Research
- Aging Biology
Background:
- Skin aging involves chronological and environmental factors like UV radiation.
- Microcirculatory changes contribute to skin aging and disease, such as psoriasis.
- Veil cells' role in vascular maintenance is not fully understood.
Purpose of the Study:
- Differentiate actinic damage from chronological aging effects on skin microvasculature.
- Investigate the role of veil cells in dermal microvessel wall changes.
- Correlate veil cell activity with aging and UV exposure.
Main Methods:
- Light and electron microscopy of skin microvessels.
- Comparison of sun-exposed versus sun-protected skin.
- Analysis of normal and psoriatic skin samples.
Main Results:
- Actinically damaged skin showed thickened vascular walls with added basement membrane-like material.
- Veil cells in damaged skin exhibited dilated endoplasmic reticulum with electron-dense material.
- Aging showed varied effects: some older individuals had thickened walls, while others had abnormally thin walls with reduced/absent veil cells.
Conclusions:
- Veil cells synthesize and maintain dermal microvessel walls.
- UV light, diabetes, and early aging stimulate excessive veil cell activity.
- Progressive aging decreases veil cell number and activity, leading to thin-walled vessels.