Seminar- Dr. Jeff Dong
Dr. Jeff Dong
MBIM Seminar Series
Starts
Mar 13, 2025 - 12:30 pmAdd to Calendar 2025-03-13 19:30:00 2025-03-13 19:30:00 Seminar- Dr. Jeff Dong

Seminar: Understanding oxidized phosphatidylcholines as key mediators of chronic neuroinflammation and neurodegeneration in multiple sclerosis

 

Abstract: Oxidized phosphatidylcholines (OxPC) are harmful byproducts of oxidative inflammation and tissue injury. While OxPC accumulate in brain lesions during neurodegenerative diseases such as multiple sclerosis (MS), their immunological and pathological functions in the central nervous system (CNS) remains relatively unknown. We aim to close this gap of knowledge by elucidating transcriptional and functional changes in the CNS of mice challenged by OxPC, followed by validation in rapid-autopsy MS brain specimens. Our findings indicate that OxPC induces progressive MS-like pathology, and that while CNS macrophages normally help to mitigate OxPC toxicity, their neuroprotective functions are disrupted by chronic neurodegeneration and aging.

LSC 2 (Life Sciences Institute - 2350 Health Sciences Mall) MBIM itsupport@microbiology.ubc.ca America/Vancouver public
Ends
Mar 13, 2025 - 1:30 pm
Location
LSC 2 (Life Sciences Institute - 2350 Health Sciences Mall)
Hosted by
Dr. Marc Horwitz
Presenter title
Assistant Professor of Immunology, Department of Biochemistry, Microbiology & Immunology, University of Saskatchewan College of Medicine
Presenter name
Dr. Jeff Dong

Seminar: Understanding oxidized phosphatidylcholines as key mediators of chronic neuroinflammation and neurodegeneration in multiple sclerosis

 

Abstract: Oxidized phosphatidylcholines (OxPC) are harmful byproducts of oxidative inflammation and tissue injury. While OxPC accumulate in brain lesions during neurodegenerative diseases such as multiple sclerosis (MS), their immunological and pathological functions in the central nervous system (CNS) remains relatively unknown. We aim to close this gap of knowledge by elucidating transcriptional and functional changes in the CNS of mice challenged by OxPC, followed by validation in rapid-autopsy MS brain specimens. Our findings indicate that OxPC induces progressive MS-like pathology, and that while CNS macrophages normally help to mitigate OxPC toxicity, their neuroprotective functions are disrupted by chronic neurodegeneration and aging.