Literature DB >> 23055261

WIS-NeuroMath enables versatile high throughput analyses of neuronal processes.

Ida Rishal1, Ofra Golani, Marek Rajman, Barbara Costa, Keren Ben-Yaakov, Zohar Schoenmann, Avraham Yaron, Ronen Basri, Mike Fainzilber, Meirav Galun.   

Abstract

Automated analyses of neuronal morphology are important for quantifying connectivity and circuitry in vivo, as well as in high content imaging of primary neuron cultures. The currently available tools for quantification of neuronal morphology either are highly expensive commercial packages or cannot provide automated image quantifications at single cell resolution. Here, we describe a new software package called WIS-NeuroMath, which fills this gap and provides solutions for automated measurement of neuronal processes in both in vivo and in vitro preparations. Diverse image types can be analyzed without any preprocessing, enabling automated and accurate detection of neurites followed by their quantification in a number of application modules. A cell morphology module detects cell bodies and attached neurites, providing information on neurite length, number of branches, cell body area, and other parameters for each cell. A neurite length module provides a solution for images lacking cell bodies, such as tissue sections. Finally, a ganglion explant module quantifies outgrowth by identifying neurites at different distances from the ganglion. Quantification of a diverse series of preparations with WIS-NeuroMath provided data that were well matched with parallel analyses of the same preparations in established software packages such as MetaXpress or NeuronJ. The capabilities of WIS-NeuroMath are demonstrated in a range of applications, including in dissociated and explant cultures and histological analyses on thin and whole-mount sections. WIS-NeuroMath is freely available to academic users, providing a versatile and cost-effective range of solutions for quantifying neurite growth, branching, regeneration, or degeneration under different experimental paradigms.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23055261     DOI: 10.1002/dneu.22061

Source DB:  PubMed          Journal:  Dev Neurobiol        ISSN: 1932-8451            Impact factor:   3.964


  28 in total

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5.  A Ca2+-Dependent Switch Activates Axonal Casein Kinase 2α Translation and Drives G3BP1 Granule Disassembly for Axon Regeneration.

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6.  Selective axonal translation of the mRNA isoform encoding prenylated Cdc42 supports axon growth.

Authors:  Seung Joon Lee; Matthew D Zdradzinski; Pabitra K Sahoo; Amar N Kar; Priyanka Patel; Riki Kawaguchi; Byron J Aguilar; Kelsey D Lantz; Caylee R McCain; Giovanni Coppola; Qun Lu; Jeffery L Twiss
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8.  Nucleolin-Mediated RNA Localization Regulates Neuron Growth and Cycling Cell Size.

Authors:  Rotem Ben-Tov Perry; Ida Rishal; Ella Doron-Mandel; Ashley L Kalinski; Katalin F Medzihradszky; Marco Terenzio; Stefanie Alber; Sandip Koley; Albina Lin; Meir Rozenbaum; Dmitry Yudin; Pabitra K Sahoo; Cynthia Gomes; Vera Shinder; Wasim Geraisy; Eric A Huebner; Clifford J Woolf; Avraham Yaron; Alma L Burlingame; Jeffery L Twiss; Mike Fainzilber
Journal:  Cell Rep       Date:  2016-07-28       Impact factor: 9.423

9.  Association of Cell Adhesion Molecules Contactin-6 and Latrophilin-1 Regulates Neuronal Apoptosis.

Authors:  Amila Zuko; Asami Oguro-Ando; Harm Post; Renske L R E Taggenbrock; Roland E van Dijk; A F Maarten Altelaar; Albert J R Heck; Alexander G Petrenko; Bert van der Zwaag; Yasushi Shimoda; R J Pasterkamp; J P H Burbach
Journal:  Front Mol Neurosci       Date:  2016-12-15       Impact factor: 5.639

10.  Schwann Cell Expressed Nogo-B Modulates Axonal Branching of Adult Sensory Neurons Through the Nogo-B Receptor NgBR.

Authors:  Christoph Eckharter; Nina Junker; Lilli Winter; Irmgard Fischer; Barbara Fogli; Steffen Kistner; Kristian Pfaller; Binhai Zheng; Gerhard Wiche; Lars Klimaschewski; Rüdiger Schweigreiter
Journal:  Front Cell Neurosci       Date:  2015-11-23       Impact factor: 5.505

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