Narrow-band UVB induces apoptosis in human keratinocytes
- PMID: 16309917
- DOI: 10.1016/j.jphotobiol.2005.08.011
Narrow-band UVB induces apoptosis in human keratinocytes
Abstract
Narrow-band ultraviolet (NB-UVB) phototherapy emits mostly 311/312 nm light and is commonly used in the treatment of inflammatory skin disorders. As a source of UVB irradiation, NB-UVB causes apoptosis in T lymphocytes but its effects on keratinocytes are unknown. Herein, we have investigated the ability of NB-UVB to induce apoptosis in keratinocytes. Two types of human keratinocytes, primary and immortalized, were exposed to NB-UVB and broad-band UVB (BB-UVB; 315-280 nm) and tested for apoptosis. Both UVB light sources induced apoptosis in keratinocytes as determined by the presence of DNA ladders, although NB-UVB required approximately ten fold higher doses; NB-UVB (1000 mJ/cm2) and BB-UVB (125 mJ/cm2). By comparison, lower doses of NB-UVB (750 mJ/cm2) induced apoptosis in T lymphocytes, suggesting cell type specificity for NB-UVB induced apoptosis. Approximately, 50% or more of the cells underwent apoptosis when exposed to NB-UVB or BB-UVB as revealed by TUNEL assay. Electron micrographs showed that NB-UVB irradiated keratinocytes contained marked chromatin condensation, extensive cytoplasmic vacuolization and fragmentation of the nuclear envelope. Furthermore, Western blot analysis confirmed the presence of activated products of caspase 3 in keratinocytes that received apoptotic doses of NB-UVB. This study defines conditions by which NB-UVB irradiation causes apoptosis in keratinocytes.
Similar articles
-
Inhibition of T helper 2 chemokine production by narrowband ultraviolet B in cultured keratinocytes.Br J Dermatol. 2007 May;156(5):830-7. doi: 10.1111/j.1365-2133.2007.07774.x. Epub 2007 Feb 20. Br J Dermatol. 2007. PMID: 17313491
-
Effects of arsenic and UVB on normal human cultured keratinocytes: impact on apoptosis and implication on photocarcinogenesis.Chem Res Toxicol. 2005 Feb;18(2):139-44. doi: 10.1021/tx049834b. Chem Res Toxicol. 2005. PMID: 15720117
-
Narrow-band UVB-induced externalization of selected nuclear antigens in keratinocytes: implications for lupus erythematosus pathogenesis.Photochem Photobiol. 2009 Jan-Feb;85(1):1-7. doi: 10.1111/j.1751-1097.2008.00480.x. Epub 2008 Dec 8. Photochem Photobiol. 2009. PMID: 19076311
-
Starting and propagating apoptotic signals in UVB irradiated keratinocytes.Photochem Photobiol Sci. 2009 Mar;8(3):299-308. doi: 10.1039/b813346h. Epub 2009 Jan 5. Photochem Photobiol Sci. 2009. PMID: 19255669 Review.
-
Effects of narrow band UVB (311 nm) irradiation on epidermal cells.Int J Mol Sci. 2013 Apr 17;14(4):8456-66. doi: 10.3390/ijms14048456. Int J Mol Sci. 2013. PMID: 23594996 Free PMC article. Review.
Cited by
-
Ultraviolet B Exposure Does Not Influence the Expression of YAP mRNA in Human Epidermal Keratinocytes-Preliminary Study.Biomedicines. 2025 Mar 1;13(3):596. doi: 10.3390/biomedicines13030596. Biomedicines. 2025. PMID: 40149574 Free PMC article.
-
Photo(chemo)therapy reduces circulating Th17 cells and restores circulating regulatory T cells in psoriasis.PLoS One. 2013;8(1):e54895. doi: 10.1371/journal.pone.0054895. Epub 2013 Jan 24. PLoS One. 2013. PMID: 23365685 Free PMC article.
-
Effect of Narrow Band Ultraviolet B Therapy versus Methotrexate on Serum Levels of Interleukin-17 and Interleukin-23 in Egyptian Patients with Severe Psoriasis.Dermatol Res Pract. 2013;2013:618269. doi: 10.1155/2013/618269. Epub 2013 Dec 31. Dermatol Res Pract. 2013. PMID: 24489536 Free PMC article.
-
Photoaging: UV radiation-induced cGAS-STING signaling promotes the aging process in skin by remodeling the immune network.Biogerontology. 2025 Jun 20;26(4):123. doi: 10.1007/s10522-025-10268-1. Biogerontology. 2025. PMID: 40542276 Free PMC article. Review.
-
The Ultraviolet Irradiation of Keratinocytes Induces Ectopic Expression of LINE-1 Retrotransposon Machinery and Leads to Cellular Senescence.Biomedicines. 2023 Nov 10;11(11):3017. doi: 10.3390/biomedicines11113017. Biomedicines. 2023. PMID: 38002016 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials