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INFORMATION FOR

    Xiaoai Zhao

    she/her/hers
    Assistant Professor
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    Contact Info

    Comparative Medicine

    333 Cedar Street, Sterling Hall of Medicine

    New Haven, CT 06510

    United States

    About

    Titles

    Assistant Professor

    Biography

    Xiaoai Zhao is an Assistant Professor in the Department of Comparative Medicine, and Yale Center for Molecular and Systems Metabolism. She completed her medical training in Nanjing China before moving to the United States. She joined John Sedivy's lab at Brown University for her graduate degree, where she studied molecular pathways of organismal aging in mouse model of longevity. She then completed her postdoctoral training in the laboratory of Anne Brunet at Stanford University. In her postdoctoral work, she investigated the functional consequences of complex lipidome changes during neural stem cell aging. Dr. Zhao joined the faculty at Yale School of Medicine in January 2024. Research in her lab focuses on the functional investigation of lipid biology in aging and age-related diseases.

    Appointments

    Education & Training

    Postdoctoral Fellow
    Stanford University (2023)
    PhD
    Brown University, Pathobiology (2015)
    MD
    Nanjing Medical University, Medicine (2008)

    Research

    Overview

    Functional regulation of lipid composition during neural stem cell aging

    We use mouse neural stem cells, a regenerative cell type in the brain, as a model in our investigation. We want to study the underlying molecular mechanisms of how complex lipids regulate cellular processes, and contribute to the functional decline during aging. Specifically, how does the composition shifts in phospholipids and sphingolipids fatty acyl side chains affect cellular function during aging. Furthermore, what are the molecular targets that regulate lipid composition-mediated impact on neural stem cell aging.

    Organelle-specific lipid regulation during aging

    Lipids are one of the most prominent structural components of organelles (e.g., nucleus, endoplasmic reticulum, Golgi apparatus, mitochondria, lysosomes and peroxisomes). We aim to characterize the organelle-specific lipidomic changes in aging cells and models of age-related diseases. We will test the hypothesis that compartment-specific lipids and lipid-derived metabolites contribute to functional deterioration during aging and age-related pathology.

    Complex lipids in systems metabolism

    Complex lipids are ubiquitous, abundant and undergo dynamic remodeling in response to different cellular and systemic conditions. These characteristics make complex lipids uniquely positioned as a key class of molecule in systems physiology. We want to probe into the ways by which complex lipids may be engaged in contributing to tissue-tissue communication through the lens of systems metabolism. Our work will reveal novel insight into the systemic contribution of complex lipids in normal physiology, aging and diseases.

    Technology development

    We believe technology is empowering in all areas of biomedical research, especially in this new frontier of lipid biology. We will continue to apply the latest technology to overcome technical limitations in addressing biological questions. We will also develop new mass spectrometry-based technologies for identifying and tracing tissue-specific lipid metabolites in studying their systemic effects on tissue and organismal health.

    Research at a Glance

    Publications Timeline

    A big-picture view of Xiaoai Zhao's research output by year.
    8Publications

    Publications

    2022

    2020

    2019

    2018

    2015

    • Reduced expression of MYC increases longevity and enhances healthspan.
      Hofmann JW, Zhao X, De Cecco M, Peterson AL, Pagliaroli L, Manivannan J, Hubbard GB, Ikeno Y, Zhang Y, Feng B, Li X, Serre T, Qi W, Van Remmen H, Miller RA, Bath KG, de Cabo R, Xu H, Neretti N, Sedivy JM. Reduced expression of MYC increases longevity and enhances healthspan. Cell 2015, 160: 477-88. PMID: 25619689, DOI: 10.1016/j.cell.2014.12.016.
      Peer-Reviewed Original Research

    2013

    • Death by transposition - the enemy within?
      Sedivy JM, Kreiling JA, Neretti N, De Cecco M, Criscione SW, Hofmann JW, Zhao X, Ito T, Peterson AL. Death by transposition - the enemy within? Bioessays 2013, 35: 1035-43. PMID: 24129940, DOI: 10.1002/bies.201300097.
      Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus Statements

    2011

    2010

    Get In Touch

    Contacts

    Mailing Address

    Comparative Medicine

    333 Cedar Street, Sterling Hall of Medicine

    New Haven, CT 06510

    United States

    Locations

    • Sterling Hall of Medicine, C-Wing

      Academic Office

      333 Cedar Street, Rm SHM-C326

      New Haven, CT 06510