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@INBOOK{Rusakov:272338,
      author       = {Zeug, André and Unichenko, Petr and Müller, Franziska E.
                      and Henneberger, Christian},
      editor       = {Rusakov, Dmitri},
      title        = {{Q}uantitative {O}ptical {A}nalysis of {A}strocytic {C}a2+
                      {S}ignaling},
      volume       = {209},
      address      = {New York, NY},
      publisher    = {Springer US},
      reportid     = {DZNE-2024-01157},
      isbn         = {978-1-0716-4010-4 (print)},
      series       = {Neuromethods},
      pages        = {21 - 57},
      year         = {2024},
      comment      = {Fluorescence Imaging of the Brain / Rusakov, Dmitri
                      (Editor) ; New York, NY : Springer US, 2024, Chapter 2 ;
                      ISSN: 0893-2336=1940-6045 ; ISBN:
                      978-1-0716-4010-4=978-1-0716-4011-1 ;
                      doi:10.1007/978-1-0716-4011-1},
      booktitle     = {Fluorescence Imaging of the Brain /
                       Rusakov, Dmitri (Editor) ; New York, NY
                       : Springer US, 2024, Chapter 2 ; ISSN:
                       0893-2336=1940-6045 ; ISBN:
                       978-1-0716-4010-4=978-1-0716-4011-1 ;
                       doi:10.1007/978-1-0716-4011-1},
      abstract     = {Ca2+ signaling of astrocytes plays a central role in the
                      physiology and pathophysiology of these non-neuronal cells
                      in the brain. Decades of research have revealed the
                      heterogeneity of astrocytic Ca2+ signals and how they are
                      triggered, how they propagate, what mechanisms sustain them,
                      and what their downstream effects are on the cellular,
                      network, and behavioral level. Imaging of astrocytic Ca2+
                      signals has been and is at the center of this research. It
                      has benefited from the development of novel indicators, of
                      new imaging techniques, and of new analytical approaches.
                      This enabled researchers to uncover a striking diversity of
                      Ca2+ signals regarding, for instance, their spatial and
                      temporal patterns, which have been linked to the operation
                      of brain circuits. When interpreting recorded Ca2+ signals
                      it needs to be considered how cellular changes of [Ca2+] are
                      reflected by the recorded fluorescence of a Ca2+ indicator,
                      what available and useful analytical approaches are, and
                      what their advantages and limitations are. Here, we provide
                      an overview of quantitative Ca2+ imaging in astrocytes by
                      covering theoretical and practical aspects of Ca2+ imaging,
                      available indicators and strategies, and toolboxes for image
                      data analysis.},
      cin          = {AG Henneberger},
      ddc          = {610},
      cid          = {I:(DE-2719)1013029},
      pnm          = {351 - Brain Function (POF4-351)},
      pid          = {G:(DE-HGF)POF4-351},
      typ          = {PUB:(DE-HGF)7},
      doi          = {10.1007/978-1-0716-4011-1_2},
      url          = {https://pub.dzne.de/record/272338},
}