Project Description: 

 

Obesity is a grave health threat. Despite extensive research and investment around the world, it remains highly challenging to overcome. The cause of obesity involves the complex interaction between gene–environment, which is mediated by epigenetic mechanisms. DNA methylation is a major epigenetic modification and we and others have demonstrate that it plays an important role in multiple aspects of adipose tissue development and function. Ten-eleventranslocation (TET) proteins are methylcytosine oxygenase and act as active DNA demethylase. Some studies have suggested that TETs may play a role in regulating in vitro adipogenesis. However, it remains unknown whether and how they regulate adipose development in vivo and what impact it has on whole body metabolism.

The goal of this proposal is to better understand how epigenetics regulates adipose tissue development and remodeling during chronic nutrition and determine the metabolic impacts, focusing on the role of TET3. Our preliminary studies have discovered that TET3 expression is induced during in vitro and in vivo adipogenesis. Tet3 deficiency in vitro inhibited adipogenesis in cultured adipocyte models. In line with this, ablation of Tet3 in PDGFRa-positive adipocyte precursor cells (APCs) led to reduced white adipose development. PDGFRa-Tet3 KO mice did not display any discernable metabolic changes when reared on a regular chow diet. However, when put on a high fat diet, the KO mice were highly resistant to diet induced obesity (DIO) with a dramatic improvement of metabolic profiles. Based upon these novel preliminary findings, we hypothesize that TET3 is a key epigenetic regulator of adipose tissue expansion and metabolism by regulating critical target genes in APCs and cell fate during diet-induced obesity.  To test that, we will assess adipogenic potential of PDGFRa+ WT and KO APCs by culturing them to adipogenesis and by performing transplanting them into WT and KO niches. To determine the role of TET3 in APC proliferation, we will assess proliferation by flow cytometry and histological analysis of WT and KO APCs in vitro and in vivo. We will analyze the full metabolic consequences of Tet3 deficiency in APCs in response to high fat diet by analyzing the detailed metabolic function of adipocytes and by assessing whole body metabolism.  These studies will elucidate how APC-specific Tet3 deficiency impact whole body metabolism and energy homeostasis in response to high fat feeding.

 

Department: 
NST
Undergraduate's Role: 

Undergrad reseachers are required to learn and assist with metabolic studies, such as insulin tolerance and glucose tolerance test, and some of  the mechanistic studies using RT-PCR, western blotting, etc. Also, we expect them to participate in weekly lab meetings.

Undergraduate's Qualifications: 

We seek someone who is mature, responsible, and serious about research. 

Location: 
On Campus
Hours: 
More than 12 hours