Abstract
Calcium acts as a prominent second messenger in virtually every cell type and modulates a plethora of cell functions. Thus, Ca2+ microfluorimetry became a valuable tool to assess information about mechanisms involved in the regulation of the intracellular calcium level in research on living tissues. Here we offer insight into distinct approaches to detect changes in calcium levels specifically in Müller cells, the principal macroglial cells of the retina.
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Acknowledgments
This work was supported by the Deutsche Forschungsgesellschaft (SPP 1172: T.P., A.R.; FOR748: A.W., A.R.; GRK 1097: A.R.; PA 615/2-1). The authors are indebted to Jens Grosche (effigos AG, www.effigos.de) for professional assistance with the illustrations.
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Wurm, A., Pannicke, T., Reichenbach, A. (2012). Ca2+ Microfluorimetry in Retinal Müller Glial Cells. In: Weber, B., LANGMANN, T. (eds) Retinal Degeneration. Methods in Molecular Biology, vol 935. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-080-9_18
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DOI: https://doi.org/10.1007/978-1-62703-080-9_18
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Publisher Name: Humana Press, Totowa, NJ
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Online ISBN: 978-1-62703-080-9
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