File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Taming microglia: the promise of engineered microglia in treating neurological diseases

TitleTaming microglia: the promise of engineered microglia in treating neurological diseases
Authors
KeywordsGlioblastoma
Microglia
Microglial genetic re-engineering
Microglial therapeutic modulation
Multiple sclerosis
Neurodegenerative diseases
Neuroinflammation
Issue Date11-Jan-2024
PublisherBioMed Central
Citation
Journal of Neuroinflammation, 2024, v. 21, n. 1 How to Cite?
Abstract

Microglia, the CNS-resident immune cells, are implicated in many neurological diseases. Nearly one in six of the world’s population suffers from neurological disorders, encompassing neurodegenerative and neuroautoimmune diseases, most with dysregulated neuroinflammation involved. Activated microglia become phagocytotic and secret various immune molecules, which are mediators of the brain immune microenvironment. Given their ability to penetrate through the blood–brain barrier in the neuroinflammatory context and their close interaction with neurons and other glial cells, microglia are potential therapeutic delivery vehicles and modulators of neuronal activity. Re-engineering microglia to treat neurological diseases is, thus, increasingly gaining attention. By altering gene expression, re-programmed microglia can be utilized to deliver therapeutics to targeted sites and control neuroinflammation in various neuroinflammatory diseases. This review addresses the current development in microglial engineering, including genetic targeting and therapeutic modulation. Furthermore, we discuss limitations to the genetic engineering techniques and models used to test the functionality of re-engineered microglia, including cell culture and animal models. Finally, we will discuss future directions for the application of engineered microglia in treating neurological diseases.


Persistent Identifierhttp://hdl.handle.net/10722/340693
ISSN
2023 Impact Factor: 9.3
2023 SCImago Journal Rankings: 2.831
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLuo, Echo Yongqi-
dc.contributor.authorSugimura, Rio Ryohichi-
dc.date.accessioned2024-03-11T10:46:27Z-
dc.date.available2024-03-11T10:46:27Z-
dc.date.issued2024-01-11-
dc.identifier.citationJournal of Neuroinflammation, 2024, v. 21, n. 1-
dc.identifier.issn1742-2094-
dc.identifier.urihttp://hdl.handle.net/10722/340693-
dc.description.abstract<p>Microglia, the CNS-resident immune cells, are implicated in many neurological diseases. Nearly one in six of the world’s population suffers from neurological disorders, encompassing neurodegenerative and neuroautoimmune diseases, most with dysregulated neuroinflammation involved. Activated microglia become phagocytotic and secret various immune molecules, which are mediators of the brain immune microenvironment. Given their ability to penetrate through the blood–brain barrier in the neuroinflammatory context and their close interaction with neurons and other glial cells, microglia are potential therapeutic delivery vehicles and modulators of neuronal activity. Re-engineering microglia to treat neurological diseases is, thus, increasingly gaining attention. By altering gene expression, re-programmed microglia can be utilized to deliver therapeutics to targeted sites and control neuroinflammation in various neuroinflammatory diseases. This review addresses the current development in microglial engineering, including genetic targeting and therapeutic modulation. Furthermore, we discuss limitations to the genetic engineering techniques and models used to test the functionality of re-engineered microglia, including cell culture and animal models. Finally, we will discuss future directions for the application of engineered microglia in treating neurological diseases.<br></p>-
dc.languageeng-
dc.publisherBioMed Central-
dc.relation.ispartofJournal of Neuroinflammation-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectGlioblastoma-
dc.subjectMicroglia-
dc.subjectMicroglial genetic re-engineering-
dc.subjectMicroglial therapeutic modulation-
dc.subjectMultiple sclerosis-
dc.subjectNeurodegenerative diseases-
dc.subjectNeuroinflammation-
dc.titleTaming microglia: the promise of engineered microglia in treating neurological diseases-
dc.typeArticle-
dc.identifier.doi10.1186/s12974-024-03015-9-
dc.identifier.scopuseid_2-s2.0-85182092304-
dc.identifier.volume21-
dc.identifier.issue1-
dc.identifier.eissn1742-2094-
dc.identifier.isiWOS:001141806900001-
dc.identifier.issnl1742-2094-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats