Dr. Ghazaleh Eskandari-Sedighi highlighted by UCI MIND

Talented UCI MIND Trainee awarded Research Fellowship

Ghazaleh Eskandar-Sedighi, PhD, is a postdoctoral fellow, supervised by Mathew Blurton-Jones, PhD, professor of Neurobiology and Behavior in the Charlie Dunlop School of Biological Sciences. Dr. Eskander-Sedighi was recently awarded a prestigious Postdoctoral Fellowship in Alzheimer’s disease research from the BrightFocus Foundation. Ghazeleh’s research focuses on leveraging human stem cell-derived microglia and chimeric animal models to investigate protective microglial responses in the context of Alzheimer’s disease (AD). Her BrightFocus Foundation project specifically aims to take advantage of novel, multi-faceted stem cell and chimeric mouse models to study the impact of the protective microglial ApoE3 Christchurch mutation on disease pathogenesis in a novel mouse model of AD with combined amyloid and tau pathologies. Considering the significant advancements in the field of microglia-based therapeutics, the results from this 2-year, $200,000 fellowship could help the field clarify the potential therapeutic role of protective variants like APOE Christchurch against AD. Congratulations Ghazeleh!

Dr. Chadarevian awarded Tom Angell Fellowship Award

UCI Mentoring Awards - UC Irvine Office of Inclusive ExcellenceDr. Jean Paul Chadarevian was awarded the 2025 Tom Angell Fellowship Award by the Office of Inclusive Excellence’s Mentoring for Achievement and Excellence. This fellowship is intended to honor Tom Angell’s contributions as the UCI Graduate Counselor to graduate student wellness and retention and signifies outstanding mentorship by going above and beyond their normal duties to create new opportunities. Congratulations, Jean Paul!

Chadarevian et al. highlighted in Alzforum

Delivery Courier? Microglia Drop Neprilysin Off Near Plaques in Brain

The blood-brain barrier border protects the brain by regulating the flow of molecules, peptides, and cells, but it also keeps out many therapeutics. Now, researchers have harnessed the power of a resident drug courier, i.e., microglia.
  • Researchers genetically engineered human iPSC-microglia to deliver neprilysin when the cells are near amyloid plaques.
  • Both local injection and brain-wide engraftment of neprilysin-secreting microglia reduced Aβ pathology.
  • Only widespread engraftment helped reduce pathologies and improve neuronal density in the subiculum.

Mathew Blurton-Jones and his team at the University of California, Irvine, have engineered human iPSC-derived microglia (iMG) to ferry protein therapeutics into the brain. They CRISPR-engineered the immune cells to express the Aβ-degrading enzyme neprilysin, but only in areas where the cells encounter amyloid plaques. When the researchers injected the couriers into mouse models of Alzheimer’s disease, the cells not only reduced the amount of amyloid, but also improved downstream aspects of Alzheimer’s pathogenesis. “While there are, of course, other approaches to reduce [Aβ] levels, this study demonstrated the powerful potential of iPSC-microglia to provide a novel immune cell therapy for a broad array of neurological diseases,” senior author Blurton-Jones wrote to Alzforum.

Read the full article here.