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Are Microglial Cells the Regulators of Lymphocyte Responses in the CNS?
Beatriz Almolda1, Berta González1, Bernardo Castellano1
1Department of Cell Biology, Physiology and Immunology, Facultat de Medicina, Institute of Neurosciences, Universitat Autònoma de Barcelona Bellaterra, Spain.
Insights
Resident glial cells and dendritic cells (DCs) communicate with T-cells in the central nervous system (CNS). This review explores how microglial cells and DCs regulate T-cell function during neuroinflammation.
Area of Science:
- Neuroimmunology
- Central Nervous System (CNS) Research
- Cellular Communication in the CNS
Background:
- Immune cell infiltration is common in neuroinflammatory conditions.
- Resident glial cells and infiltrated immune cells, including T-cells, interact within the CNS.
- Dendritic cells (DCs) are present in specific CNS locations and their precursors may infiltrate during neuroinflammation.
Purpose of the Study:
- To review the molecules involved in T-cell cross-talk by microglial cells and DCs.
- To discuss the role of microglial cells and DCs in regulating T-cell function within the CNS.
- To highlight the potential contribution of these cells in neuroinflammatory settings.
Main Methods:
- Literature review of studies on microglial cells and dendritic cells in the CNS.
- Analysis of molecular mechanisms underlying cell-cell communication.
- Synthesis of current knowledge on T-cell regulation by glial and dendritic cells.
Main Results:
- Microglial cells can adopt a dendritic cell (DC) phenotype under certain conditions.
- Both microglial cells and DCs express molecules crucial for T-cell interaction.
- These cells potentially regulate T-cell recruitment, activation, and function in the CNS.
Conclusions:
- Microglial cells and DCs play significant roles in modulating T-cell responses within the CNS.
- Understanding this cross-talk is vital for comprehending neuroinflammatory processes.
- Further research into these cellular interactions may reveal therapeutic targets for CNS disorders.
Abstract:
The infiltration of immune cells in the central nervous system is a common hallmark in different neuroinflammatory conditions. Accumulating evidence indicates that resident glial cells can establish a cross-talk with infiltrated immune cells, including T-cells, regulating their recruitment, activation and function within the CNS. Although the healthy CNS has been thought to be devoid of professional dendritic cells (DCs), numerous studies have reported the presence of a population of DCs in specific locations such as the meninges, choroid plexuses and the perivascular space. Moreover, the infiltration of DC precursors during neuroinflammatory situations has been proposed, suggesting a putative role of these cells in the regulation of lymphocyte activity within the CNS. On the other hand, under specific circumstances, microglial cells are able to acquire a phenotype of DC expressing a wide range of molecules that equip these cells with all the necessary machinery for communication with T-cells. In this review, we summarize the current knowledge on the expression of molecules involved in the cross-talk with T-cells in both microglial cells and DCs and discuss the potential contribution of each of these cell populations on the control of lymphocyte function within the CNS.
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