Low dose ionizing radiation-induced activation of connexin 43 expression

• Published in: International journal of radiation biology Vol. 79; no. 12; pp. 955 - 964
• Main Authors: Glover, D., Little, J. B., Lavin, M. F., Gueven, N.
• Format: Journal Article
• Language: English
• Published: London Informa UK Ltd 01.12.2003; Taylor & Francis
• Subjects: Amino Acid Sequence; Biological and medical sciences; Connexin 43 - biosynthesis; Connexin 43 - chemistry; Connexin 43 - genetics; Dose-Response Relationship, Radiation; Fibroblasts - metabolism; Fibroblasts - radiation effects; Gene Expression Regulation - radiation effects; HeLa Cells; Humans; Medical sciences; Molecular Sequence Data; Mutation; Radiation Dosage; Radiation, Ionizing; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects); Sequence Analysis, Protein; Technology. Biomaterials. Equipments. Material. Instrumentation; Transcriptional Activation - radiation effects; Up-Regulation - radiation effects; Biomedical engineering
• ISSN: 0955-3002; 1362-3095
• DOI: 10.1080/09553000310001632895

Purpose: Connexin 43 has been implicated in the cellular response to ionizing radiation by enabling cell-to-cell communication. It is established here that the expression of connexin 43 is affected by ionizing radiation and the mechanism involved is investigated. Materials and methods: The human connexin 43 promoter was cloned into a Luciferase reporter plasmid and activation by ionizing radiation was measured in normal human fibroblasts as well as HeLa cells. The regions responsible for the radiation inducibility were defined using deletion and point mutations of the construct. The results were confirmed by Northern and Western blotting. Results: Ionizing radiation activates the human connexin 43 promoter in a time- and dose-dependent manner with a maximal induction (4.2-fold ±0.58) after 6 h and a dose of 0.5 Gy. Higher doses up to 5 Gy led to a less marked increase (2-fold) over the same period. This promoter activation was associated with comparable increases in both connexin 43 mRNA and protein levels. The low dose radiation response of the promoter is mainly dependent on consensus binding sites for nuclear factor of activated T-cells (NFAT) and activator protein (AP1) in a region −2537 and −2110 bp from the transcriptional start site as determined by mutation analysis. Conclusions: Low doses of ionizing radiation induce the transcriptional upregulation of connexin 43 expression employing NFAT and AP1 sites.