A single dose of radiation elicits comparable acute salivary gland injury to fractionated radiation.
Amanda L JohnsonSonia S ElderJohn G McKendrickLizi M HegartyElla MercerElaine EmmersonPublished in: Disease models & mechanisms (2024)
The salivary glands are often damaged during head and neck cancer radiotherapy. This results in chronic dry mouth, which adversely affects quality of life and for which there is no long-term cure. Mouse models of salivary gland injury are routinely used in regenerative research. However, there is no clear consensus on the radiation regime required to cause injury. Here, we analysed three regimes of γ-irradiation of the submandibular salivary gland. Transcriptional analysis, immunofluorescence and flow cytometry was used to profile DNA damage, gland architecture and immune cell changes 3 days after single doses of 10 or 15 Gy or three doses of 5 Gy. Irrespective of the regime, radiation induced comparable levels of DNA damage, cell cycle arrest, loss of glandular architecture, increased pro-inflammatory cytokines and a reduction in tissue-resident macrophages, relative to those observed in non-irradiated submandibular glands. Given these data, coupled with the fact that repeated anaesthetic can negatively affect animal welfare and interfere with saliva secretion, we conclude that a single dose of 10 Gy irradiation is the most refined method of inducing acute salivary gland injury in a mouse model.
Keyphrases
- radiation induced
- dna damage
- mouse model
- radiation therapy
- flow cytometry
- liver failure
- cell cycle arrest
- oxidative stress
- stem cells
- dna repair
- drug induced
- respiratory failure
- cell death
- gene expression
- early stage
- small cell lung cancer
- electronic health record
- transcription factor
- patient safety
- squamous cell carcinoma
- machine learning
- quality improvement
- extracorporeal membrane oxygenation
- data analysis
- tissue engineering