Astrocytes react to the presence of extracellular amyloid-β aggregates in the aging brain by becoming more inflammatory and clustering around the aggregates of misfolded proteins. Researchers here show that this activity crowds out the microglia responsible for ingesting and breaking down these protein aggregates. The crowding can, however, be controlled to some degree by targeting plexin-B1, allowing microglia access to conduct greater clearance of amyloid-β. This is early stage research, so it remains to be seen as to whether it will actually offer a way to make forms of anti-amyloid therapies more effective, or can be the basis for such a therapy itself.
Researchers have made a significant breakthrough in Alzheimer's disease research by identifying a novel way to potentially slow down or even halt disease progression. The study, which focuses on the role of reactive astrocytes and the plexin-B1 protein in Alzheimer's pathophysiology, provides crucial insights into brain cell communication and opens the door to innovative treatment strategies. This groundbreaking work is centered on the downregulation of the plexin-B1 protein to enhance the brain's ability to clear amyloid plaques, a hallmark of Alzheimer's disease. Reactive astrocytes, a type of brain cell that becomes activated in response to injury or disease, were found to play a crucial role in this process. They help control the spacing around amyloid plaques, affecting how other brain cells can access and clear these harmful deposits.
Link: https://www.eurekalert.org/news-releases/1045861
