Programme(s) to which this project applies:
|☑ MPhil/PhD||☒ MRes[Med]||☒ URIS|
In contrast to white adipose tissue (WAT) that stores energy, brown adipose tissue (BAT) is specialised for energy dissipation and considered as a potential weapon to combat obesity by uncoupling mitochondrial respiratory chain and ATP synthesis. Recently, the ‘inducible’ brown adipocytes, denoted as ‘beige’ cells, were found scattering within the WAT. Animal-based studies have shown that functional beige or brown adipocytes possess multiple metabolic benefits independent of its adiposity-reducing effect, including insulin sensitising, lipid lowering, anti-inflammatory and anti-atherosclerotic effects.
In adult human, a significant amount of active brown/beige adipose tissue has been detected by positron emission tomography (PET) and its amount/activity is inversely related to ageing, obesity and a cluster of cardio-metabolic diseases. Moreover, activation of brown/beige adipocytes in human by cold acclimation confers protection against a series of metabolic disorders. Notably, beiging of WAT requires participation of immune responses. We have discovered that adipokines, including adiponectin and FGF21, contribute to cold-induced beige cell biogenesis by fostering the type 2 immune responses in WAT, which involves sequential activation of IL-C2 cells, eosinophils and M2 macrophages. However, whether and how other immune cells are involved in this process is unknown.
Compared to the RNA-sequencing-based bulk analysis, single cell sequencing examines the sequence information from individual cells, facilitating a higher resolution of cellular differences and a better understanding of the function of an individual cell in the context of its microenvironment. Therefore, in order to gain a further insight into the immunological events underlying brown remodelling of WAT, we will perform single cell sequencing analysis in mouse WAT before and after cold-induced browning. The novel immune cells involved will be identified. Cell and animal-based studies will be carried out to further elucidate the molecular mechanisms whereby the immune cell integrates into the immune-metabolism network during adipose browning. The findings will also be verified in human adipose biopsies so as to explore the clinical relevance of the study. Implementation of the study will identify novel factors/pathways that engage WAT browning, and thereby provide new targets for treatment of obesity and metabolic complications.
Professor A Xu, Department of Medicine
Professor Aimin Xu has been focusing on both basic and translational research on obesity/diabetes-related disorders. He is leading the State Key Laboratory of Pharmaceutical Biotechnology, which is at the forefront of innovation and discovery in the field of molecular metabolism, with a focus on hormones and biomarkers. Professor Xu has made significant contributions to discovery and functional characterisation of several adipokines and hormones including adiponectin, fibroblast growth factor 21 (FGF21), adipocyte-fatty acid binding protein (A-FABP) and lipocalin-2.
For more information or to express interest for this project, please email the supervisor or the specified contact point in the project description. Interested candidates are advised to enclose with your email:
Information on the research programme, funding support and admission documentations could be referenced online at the Research Postgraduate Admissions website. General admission enquiries should be directed to firstname.lastname@example.org.
HKUMed MBBS students interested in the Master of Research in Medicine (MRes[Med]) programme may visit the programme website for more information.
HKUMed UG students interested in the Undergraduate Research Internship Scheme (URIS) may visit the scheme’s website for more information.