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Updated: Feb 23, 2026

Modulation of Tau Subcellular Localization as a Tool to Investigate the Expression of Disease-related Genes
Published on: December 20, 2019
Digital quantification of neurite outgrowth and retraction by phase-contrast microscopy: A tau perspective
Brett Cook1, Duncan Proctor2, Rachel Bromberg2
1Neuroscience Research Institute, University of California Santa Barbara, Santa Barbara, CA, United States; Program in Biomolecular Science and Engineering, University of California Santa Barbara, Santa Barbara, CA, United States.
Abstract:
The proper organization and function of the mammalian nervous system relies on neuronal processes or "neurites," extended morphological projections that include axons and dendrites. Tau is a structural microtubule-associated protein that is widely expressed in the nervous system that mediates the establishment of cell polarity, neurite outgrowth, and axonal transport. A useful model for studying the establishment and maintenance of these neuronal structures are rat neuronal PC12 cells, which can be induced to express tau and project neurites by treating the cells with nerve growth factor. Here, we present a simple method for continuously measuring the rate of neurite outgrowth and retraction over time by neurite length and neurite area analyses. This method uses freely available ImageJ software and widely available phase-contrast imaging.

