|Funding for:||UK Students, EU Students|
|Funding amount:||Not Specified|
|Placed On:||25th October 2021|
|Closes:||16th December 2021|
Applications accepted up to Thursday 16th December 2021, 5pm
1st Supervisor: Dr. Elaine Emmerson (University of Edinburgh)
About the Project
Radiation injury is characterised by an influx of inflammatory cells. Macrophages have long been considered key cells in the tissue repair process, but they can have both beneficial and detrimental effects on damage resolution and tissue repair, depending on their phenotype and the niche they inhabit. The salivary glands (SG) are often inadvertently irradiated during treatment for head and neck cancer; however, our understanding of the cellular and molecular processes that govern effective tissue repair and regeneration in the irradiated SG remains incomplete. The Emmerson lab (1st supervisor) have recently demonstrated that distinct populations of macrophages exist in the mouse and human salivary glands. Furthermore, we have shown that irradiation (IR) injury causes significant changes in the phenotype of some of these populations, suggesting that IR injury may directly or indirectly influence macrophage functions. Finally, we have shown that in the absence of macrophages, epithelial DNA damage accumulates, demonstrating that macrophages are essential for efficient repair (in collaboration with the Bain lab, 3rd supervisor).
Next, we want to determine if macrophage phenotype is important for their role in SG repair after injury, and whether we can help SG regeneration occur more efficiently by specifically targeting the macrophages to develop a particular phenotype.
In this project the student will:
Overall, this will determine if macrophage manipulation can be used as a therapeutic tool to promote salivary gland regeneration.
The student will use in vivo mouse models, ex vivo assays, cell culture, pharmacological experiments, multicolour flow cytometry and fluorescence-activated cell sorting (FACS), high powered confocal microscopy and transcriptional analysis, including the analysis of single cell (sc)-RNA-seq data, in order to address these aims. Furthermore, the student will gain experience in report writing, oral presentation, statistics and data management.
UKRI-funded studentships are open to students worldwide and will cover tuition fees at the UK rate, plus a stipend to support living costs and an annual research grant of £5,000 for the first three years of the PhD research. For further details on funding eligibility and how to apply, please see link below
The EASTBIO team will run a series of 1-hour online sessions in November/December, open to applicants who have queries about the application process. Please view EASTBIO How to Apply webpage for details.
Unfortunately due to workload constraints, we cannot consider incomplete applications.
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