Understanding Glial Signaling in Neurodegeneration via Gene Network Analysis
Principal Investigator
Co-Principal Investigator
Project Goals
Recent scientific discoveries suggest that multiple cell types might participate in Alzheimer’s disease (AD), and understanding the key players and their effects on dementia would advance our ability to design new drugs and therapies. However, the complexity of the brain’s different cell types presents a unique challenge to scientific inquiry. Here I propose work to bridge the divide by using cutting edge technology to profile the different cells of the dementia brain at unprecedented resolution. The results of this work will be new candidate drug targets for dementia and a new approach for studying complex brain diseases.
Project Summary
Alzheimer’s disease (AD) has traditionally been studied one gene, cell type, or biological process at a time; however, it is increasingly clear that this disease involves multiple interacting cell types and pathways within those cells. We currently lack a refined view of AD from the cellular and multicellular levels. Such an understanding would advance data driven approaches to identify disease mechanisms and inform rational drug design. Transcriptomic network analysis and functional genomics approaches performed at the whole tissue level have uncovered a complex role for neuron-glial interactions. However, glial contributions to disease are particularly challenging to identify by these methods in whole tissue alone due to complex transcellular interactions and functional heterogeneity among glia, for example, microglia and astrocytes. The objective of this proposal is to complete longitudinal single-cell transcriptional profiling and integrate the results with data from mouse models and human disease, to add the cellular resolution needed to fully leverage transcriptomic networks to understand glial signaling mechanisms in AD.
Publications
Rexach JE, Polioudakis D, Yin A, Swarup V, Chang TS, Nguyen T, Sarkar A, Chen L, Huang J, Lin LC, Seeley W, Trojanowski JQ, Malhotra D, Geschwind DH. Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression. Cell Rep. 2020 Nov 17;33(7):108398. doi: 10.1016/j.celrep.2020.108398. PMID: 33207193. 
More Information
About Jessica Rexach, MD, PhD
Dr. Rexach earned her BA degrees in Chemistry and Biology at Cornell University in 2003. She subsequently entered the joint MD PhD program between California Institute of Technology and University of California, Los Angeles, completing her medical degree and doctoral degree in Neuroscience (with a research focus in Chemical Biology) in 2012. Her graduate work resulted in three first author publications in Nature Chemical Biology. She completed a medical internship at Cedars Sinai Medical Center and a residency in Neurology at University of California, Los Angeles. She subsequently completed a competitive NIH-sponsored joint research and clinical fellowship in Neurogenetics and Neurobehavior at University of California, Los Angeles. Dr. Rexach is currently an attending physician in the UCLA Neurogenetics Program with clinical specialty in neurodegenerative disorders affecting cognition and dementia. She is concurrently completing her postdoctoral research training in the laboratory of Dr. Geschwind. Dr. Rexach’s research uses human genetics and systems biology to understand immune signaling in Alzheimer’s and associated dementias with the goal of developing immune-targeted therapies.
Throughout her education and training, Dr. Rexach has been recognized for excellence in teaching, clinical care, and science. She has received numerous awards including the August Rose Award for Excellence in Teaching and J. Louis Riehl Research Award from the UCLA Department of Neurology, Leo G. Rigler Award for Outstanding Achievement as a medical intern from Cedars Sinai Medical Center, Emil Bogen Research Prize from the UCLA School of Medicine, and Leo and Berdie Mandelkern Prize in Chemistry from Cornell University.
Dr. Rexach's Personal Story
I was born a city girl but my formative years were spent in the mountains of California’s gold country in the small and quiet town of Mariposa. Even as a child, I had an unstoppable internal drive to share my ideas and contribute to fixing big problems in the world. The desire to make a difference in dementia led me on my path as a physician scientist. I believe a physician scientist is tasked to seek out, adopt or create whatever scientific tools are necessary to meet their clinical goal. The caveat is that this takes exceptional mentorship and training to achieve. It is from that view that I chose to train in Chemical Biology under Linda Hsieh-Wilson at California Institute of Technology and develop skills in creating chemical and biological tools to meet gaps in molecular biology. It was the same view that led me to expand into systems biology, genetics, and bioinformatics with my post-doctoral research training, in order to develop the skills to use human data to guide my experimental science. In this work, I have had the remarkable privilege to train under Dr. Daniel Geschwind who is a pioneer in applying systems biology and data science to tackle the critical unknowns in neuropsychiatric disease. This data-driven approach has led me to the study of immune signaling and the interaction of different brain cell types in dementia. I reason that immune signals offer key access points for the development of clinical biomarkers and drug development in dementia, and that a systems view will provide insightful perspective on how to address the rational design of dementia therapies.
First published on: January 08, 2019
Last modified on: November 20, 2024