Human Glial Cells as Innovative Targets for the Therapy of Central Nervous System Pathologies.

Cells

Laboratory of Pain Therapy and Neuroimmunology, Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133 Milan, Italy.

Published: March 2024

AI Article Synopsis

  • Preclinical research over the past 35 years has shown that glial cells, like astrocytes and microglia, play a critical role in brain health and diseases, impacting neurodegeneration and pain.
  • Several potential drug targets have been identified, including receptors and enzymes involved in neuroinflammation, but translating these findings into clinical treatments faces significant challenges.
  • The review will focus on the role of glial cells in human diseases, discussing findings from post-mortem studies and human cell models, as well as the potential for visualizing glial responses to neuroinflammation in patients.

Article Abstract

and preclinical research in the last 35 years has clearly highlighted the crucial physiopathological role of glial cells, namely astrocytes/microglia/oligodendrocytes and satellite glial cells/Schwann cells in the central and peripheral nervous system, respectively. Several possible pharmacological targets to various neurodegenerative disorders and painful conditions have therefore been successfully identified, including receptors and enzymes, and mediators of neuroinflammation. However, the translation of these promising data to a clinical setting is often hampered by both technical and biological difficulties, making it necessary to perform experiments on human cells and models of the various diseases. In this review we will, therefore, summarize the most relevant data on the contribution of glial cells to human pathologies and on their possible pharmacological modulation based on data obtained in post-mortem tissues and in iPSC-derived human brain cells and organoids. The possibility of an visualization of glia reaction to neuroinflammation in patients will be also discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11011741PMC
http://dx.doi.org/10.3390/cells13070606DOI Listing

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