Unknown

Dataset Information

0

Ultraviolet radiation damages self noncoding RNA and is detected by TLR3.


ABSTRACT: Exposure to ultraviolet B (UVB) radiation from the sun can result in sunburn, premature aging and carcinogenesis, but the mechanism responsible for acute inflammation of the skin is not well understood. Here we show that RNA is released from keratinocytes after UVB exposure and that this stimulates production of the inflammatory cytokines tumor necrosis factor ? (TNF-?) and interleukin-6 (IL-6) from nonirradiated keratinocytes and peripheral blood mononuclear cells (PBMCs). Whole-transcriptome sequencing revealed that UVB irradiation of keratinocytes induced alterations in the double-stranded domains of some noncoding RNAs. We found that this UVB-damaged RNA was sufficient to induce cytokine production from nonirradiated cells, as UVB irradiation of a purified noncoding RNA (U1 RNA) reproduced the same response as the one we observed to UVB-damaged keratinocytes. The responses to both UVB-damaged self-RNAs and UVB-damaged keratinocytes were dependent on Toll-like receptor 3 (TLR3) and Toll-like receptor adaptor molecule 1 (TRIF). In response to UVB exposure, Tlr3(-/-) mice did not upregulate TNF-? in the skin. Moreover, TLR3 was also necessary for UVB-radiation-induced immune suppression. These findings establish that UVB damage is detected by TLR3 and that self-RNA is a damage-associated molecular pattern that serves as an endogenous signal of solar injury.

SUBMITTER: Bernard JJ 

PROVIDER: S-EPMC3812946 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications


Exposure to ultraviolet B (UVB) radiation from the sun can result in sunburn, premature aging and carcinogenesis, but the mechanism responsible for acute inflammation of the skin is not well understood. Here we show that RNA is released from keratinocytes after UVB exposure and that this stimulates production of the inflammatory cytokines tumor necrosis factor α (TNF-α) and interleukin-6 (IL-6) from nonirradiated keratinocytes and peripheral blood mononuclear cells (PBMCs). Whole-transcriptome s  ...[more]

Similar Datasets

| S-EPMC5933051 | biostudies-literature
| S-EPMC3384068 | biostudies-literature
| S-EPMC3287179 | biostudies-literature
| S-EPMC5105223 | biostudies-literature
2020-04-14 | GSE137226 | GEO
| S-EPMC7268463 | biostudies-literature
| 2330122 | ecrin-mdr-crc
| S-EPMC8605545 | biostudies-literature
| S-EPMC7497027 | biostudies-literature
| S-EPMC6883822 | biostudies-literature