001     271880
005     20240913103952.0
020 _ _ |a 978-3-031-55528-2 (print)
020 _ _ |a 978-3-031-55529-9 (electronic)
024 7 _ |a 10.1007/978-3-031-55529-9_5
|2 doi
024 7 _ |a pmid:39207687
|2 pmid
037 _ _ |a DZNE-2024-01092
041 _ _ |a English
100 1 _ |a Crockett, Alexis
|b 0
245 _ _ |a Progress in Structural and Functional In Vivo Imaging of Microglia and Their Application in Health and Disease.
260 _ _ |a Cham
|c 2024
|b Springer International Publishing
295 1 0 |a Microglia / Tremblay, Marie-Ève (Editor) ; Cham : Springer International Publishing, 2024, Chapter 5 ; ISSN: 2190-5215=2190-5223 ; ISBN: 978-3-031-55528-2=978-3-031-55529-9 ; doi:10.1007/978-3-031-55529-9
300 _ _ |a 65 - 80
336 7 _ |a BOOK_CHAPTER
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336 7 _ |a Book Section
|0 7
|2 EndNote
336 7 _ |a bookPart
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336 7 _ |a INBOOK
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336 7 _ |a Output Types/Book chapter
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336 7 _ |a Contribution to a book
|b contb
|m contb
|0 PUB:(DE-HGF)7
|s 1726216731_2424
|2 PUB:(DE-HGF)
490 0 _ |a Advances in Neurobiology
|v 37
520 _ _ |a The first line of defense for the central nervous system (CNS) against injury or disease is provided by microglia. Microglia were long believed to stay in a dormant/resting state, reacting only to injury or disease. This view changed dramatically with the development of modern imaging techniques that allowed the study of microglial behavior in the intact brain over time, to reveal the dynamic nature of their responses. Over the past two decades, in vivo imaging using multiphoton microscopy has revealed numerous new functions of microglia in the developing, adult, aged, injured, and diseased CNS. As the most dynamic cells in the brain, microglia continuously contact all structures and cell types, such as glial and vascular cells, neuronal cell bodies, axons, dendrites, and dendritic spines, and are believed to play a central role in sculpting neuronal networks throughout life. Following trauma, or in neurodegenerative or neuroinflammatory diseases, microglial responses range from protective to harmful, underscoring the need to better understand their diverse roles and states in different pathological conditions. In this chapter, we introduce multiphoton microscopy and discuss recent advances in structural and functional imaging technologies that have expanded our toolbox to study microglial states and behaviors in new ways and depths. We also discuss relevant mouse models available for in vivo imaging studies of microglia and review how such studies are constantly refining our understanding of the multifaceted role of microglia in the healthy and diseased CNS.
536 _ _ |a 352 - Disease Mechanisms (POF4-352)
|0 G:(DE-HGF)POF4-352
|c POF4-352
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef Book Series, PubMed, , Journals: pub.dzne.de
650 _ 7 |a Alzheimer’s disease
|2 Other
650 _ 7 |a Imaging technologies and methods
|2 Other
650 _ 7 |a In vitro experiments
|2 Other
650 _ 7 |a In vivo imaging
|2 Other
650 _ 7 |a Microglia
|2 Other
650 _ 7 |a Mouse models
|2 Other
650 _ 7 |a Multiple sclerosis
|2 Other
650 _ 7 |a Two-photon microscopy
|2 Other
650 _ 2 |a Microglia: metabolism
|2 MeSH
650 _ 2 |a Microglia: pathology
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Microscopy, Fluorescence, Multiphoton
|2 MeSH
650 _ 2 |a Brain: diagnostic imaging
|2 MeSH
650 _ 2 |a Neuroinflammatory Diseases: diagnostic imaging
|2 MeSH
650 _ 2 |a Neuroinflammatory Diseases: pathology
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: diagnostic imaging
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: pathology
|2 MeSH
700 1 _ |a Fuhrmann, Martin
|0 P:(DE-2719)2679991
|b 1
|u dzne
700 1 _ |a Garaschuk, Olga
|b 2
700 1 _ |a Davalos, Dimitrios
|b 3
773 _ _ |a 10.1007/978-3-031-55529-9_5
856 4 _ |u https://pub.dzne.de/record/271880/files/DZNE-2024-01092_Restricted.pdf
856 4 _ |u https://pub.dzne.de/record/271880/files/DZNE-2024-01092_Restricted.pdf?subformat=pdfa
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909 C O |p VDB
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 1
|6 P:(DE-2719)2679991
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-352
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
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|v Disease Mechanisms
|x 0
914 1 _ |y 2024
920 1 _ |0 I:(DE-2719)1011004
|k AG Fuhrmann
|l Neuroimmunology and Imaging
|x 0
980 _ _ |a contb
980 _ _ |a VDB
980 _ _ |a I:(DE-2719)1011004
980 _ _ |a UNRESTRICTED


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