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Published on: March 2, 2011
Interleukin-1 alpha in human sweat is functionally active and derived from the eccrine sweat gland
1Marshall Dermatology Research Laboratories, Department of Dermatology, University of Iowa College of Medicine, Iowa City 52242-1181.
Insights
Interleukin-1 (IL-1) alpha is present in human sweat, originating from sweat glands. This biologically active substance stimulates other inflammatory cytokines, suggesting a role in skin immunity.
Area of Science:
- Immunology
- Dermatology
- Human Physiology
Background:
- Interleukin-1 (IL-1) is a key inflammatory cytokine.
- Its presence and role in human sweat were previously unclear.
Purpose of the Study:
- To confirm the presence of IL-1 in human sweat.
- To determine the origin and secretion mechanism of IL-1 in sweat.
- To assess the biological activity of sweat IL-1.
Main Methods:
- Quantification of IL-1 alpha and IL-1 beta in sweat samples from different body sites.
- Western blot analysis and immunohistochemistry for IL-1 alpha.
- Polymerase chain reaction (PCR) for IL-1 alpha mRNA detection.
- In vitro assays measuring fibroblast response to sweat IL-1.
Main Results:
- IL-1 alpha concentration in sweat increased with sweat rate, with higher levels in women than men.
- Significant IL-1 alpha and IL-1 beta levels were found in palmar sweat.
- IL-1 alpha mRNA and protein were detected within sweat glands and cultured eccrine cells.
- Sweat IL-1 alpha stimulated the production of IL-6 and IL-8 in fibroblasts.
Conclusions:
- The substance in sweat is indeed IL-1 alpha, originating from the sweat gland.
- IL-1 alpha in sweat is biologically active at physiological concentrations.
- Sweat glands are a source of biologically active IL-1 alpha, potentially contributing to skin immune responses.
Abstract:
We wished to establish the presence of interleukin-1 (IL-1) in human sweat (5) and clarify its origin and mechanism of secretion. IL-1 alpha concentration ([IL-1 alpha]) in clean sweat from the back increased with the sweat rate, plateauing at the maximal sweat rate ([IL-1 alpha]max). The mean [IL-1 alpha]max was 545 pg/ml (n = 17) for men and 1,324 pg/ml for women in back sweat. The mean [IL-1 alpha]max for axillary sweat in men was 1,568 (n = 6). Palmar sweat was 9.2 ng/ml (n = 5) for IL-1 alpha and 7.9 ng/ml for IL-1 beta. [IL-1 alpha]max decreased to one-third that of the first sweat test, when second sauna sweat tests were conducted after 2 h of continuous sweating on the same day. Western blot analysis of the purified sweat IL-1 alpha fraction revealed bands at 17, 29, and 33 kDa. Immunoreactive IL-1 alpha was localized mainly in the secretory coil lumen, intercellular canaliculi, cytoplasm, mitochondria, and near plasma membranes. Polymerase chain reaction revealed the presence of IL-1 alpha mRNA in the sweat gland and in cultured human eccrine secretory coil cells. Both sweat IL-1 alpha and human recombinant IL-1 alpha at 500 pg/ml strongly stimulated interleukin-6 and interleukin-8 production in cultured fibroblasts. We conclude that the IL-1 alpha-like immunoreactive substance in sweat is IL-1 alpha itself, is derived from the sweat gland, and is biologically active at concentrations normally present in fresh sweat.
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