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Updated: Aug 8, 2026

Imaging Local Ca2+ Signals in Cultured Mammalian Cells
Published on: March 3, 2015
Visualizing calcium signaling in cells by digitized wide-field and confocal fluorescent microscopy
Michael W Roe1, Jerome F Fiekers, Louis H Philipson
1Department of Medicine, University of Chicago, IL, USA.
Abstract:
Calcium (Ca2+) is a fundamentally important component of cellular signal transduction. Dynamic changes in the concentration of Ca2+ ([Ca2+]) in the cytoplasm and within organelles are tightly controlled and regulate a diverse array of biological activities, including fertilization, cell division, gene expression, cellular metabolism, protein biosynthesis, secretion, muscle contraction, intercellular communication, and cell death. Measurement of intracellular [Ca2+] is essential to understanding the role of Ca2+ and for defining the underlying regulatory mechanisms in any cellular process. A broad range of synthetic and biosynthetic fluorescent Ca2+ sensors are available that enable the visualization and quantification of subcellular spatio-temporal [Ca2+] gradients. This chapter describes the application of wide-field digitized video fluorescence microfluorometry and confocal microscopy to quantitatively image Ca2+ in cells with high temporal and spatial resolution.

