Related Experiment Video
Updated: Jun 3, 2026

Obtaining Human Microglia from Adult Human Brain Tissue
Published on: August 30, 2020
The role of microglial cell subsets in Alzheimer's disease
1Laboratory of Endocrinology and Genomics, CHUL Research Center and, Department of Molecular Medicine, Faculty of Medicine, Laval University, 2705 Laurier boul., Québec, G1V 4G2, Canada.
Abstract:
Alzheimer disease (AD) is characterized by a progressive cognitive decline and accumulation of β-amyloid (Aβ forming senile plaques that are associated with inflammatory molecules and cells. Resident microglia and newly differentiated cells that are derived from the bone marrow are found in the vicinity of Aβ plaques. Although these two types of microglia are not distinguishable by specific markers in the brain, they seem to possess different phenotype and functions. In mouse models of AD, bone marrow-derived microglia (BMDM) have been shown to delay or stop the progression of AD and preventing their recruitment exacerbates the pathology. Transplantation of competent hematopoietic stem cells or their genetic modifications ameliorate cognitive functions, reduce Aβ accumulation and prevent synaptic dysfunctions. Improving the recruitment of genetically-modified BMDM may be considered as a powerful new therapeutic strategy to counteract AD. Here we review the role of microglia subsets in AD and how these cells have a great potential to fight against Aβ accumulation and cognitive impairment.
Insights
Bone marrow-derived microglia (BMDM) show potential in combating Alzheimer disease (AD) by reducing amyloid-beta plaques and improving cognitive function. Enhancing BMDM recruitment offers a promising therapeutic avenue for AD.
Area of Science:
- Neuroscience
- Immunology
- Pathology
Background:
- Alzheimer disease (AD) involves cognitive decline and amyloid-beta (Aβ) plaque accumulation.
- Microglia, including resident and bone marrow-derived cells, are present near Aβ plaques.
- These microglial subsets may have distinct functions in AD pathology.
Purpose of the Study:
- To review the role of different microglial subsets in Alzheimer disease.
- To explore the therapeutic potential of bone marrow-derived microglia (BMDM) in counteracting AD.
- To highlight strategies for improving BMDM recruitment for AD treatment.
Main Methods:
- Review of existing literature on microglia in Alzheimer disease models.
- Analysis of studies investigating the effects of bone marrow-derived microglia (BMDM) on AD progression.
- Examination of therapeutic strategies involving hematopoietic stem cell transplantation or genetic modification.
Main Results:
- Bone marrow-derived microglia (BMDM) can delay or halt Alzheimer disease progression in mouse models.
- Preventing BMDM recruitment exacerbates AD pathology.
- Transplantation or genetic modification of hematopoietic stem cells can improve cognitive function and reduce Aβ burden.
Conclusions:
- Microglia subsets play a critical role in Alzheimer disease.
- Genetically-modified bone marrow-derived microglia (BMDM) offer a potent therapeutic strategy for AD.
- Enhancing BMDM recruitment is a promising approach to combat Aβ accumulation and cognitive impairment in Alzheimer disease.
Related Concept Videos
Alzheimer Disease ll: Pathophysiology
Alzheimer's Disease: Overview
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ and tau...
Glial Cells
Nervous Tissue: Glial Cells
The CNS glial cell includes the astrocytes, the oligodendrocytes, the microglia, and the ependymal cells.
Astrocytes are star-shaped glial cells that interact...
Alzheimer Disease l: Introduction
