Literature DB >> 28689759

Amplification of F-Actin Disassembly and Cellular Repulsion by Growth Factor Signaling.

Jimok Yoon1, Sang Bum Kim2, Giasuddin Ahmed1, Jerry W Shay2, Jonathan R Terman3.   

Abstract

Extracellular cues that regulate cellular shape, motility, and navigation are generally classified as growth promoting (i.e., growth factors/chemoattractants and attractive guidance cues) or growth preventing (i.e., repellents and inhibitors). Yet, these designations are often based on complex assays and undefined signaling pathways and thus may misrepresent direct roles of specific cues. Here, we find that a recognized growth-promoting signaling pathway amplifies the F-actin disassembly and repulsive effects of a growth-preventing pathway. Focusing on Semaphorin/Plexin repulsion, we identified an interaction between the F-actin-disassembly enzyme Mical and the Abl tyrosine kinase. Biochemical assays revealed Abl phosphorylates Mical to directly amplify Mical Redox-mediated F-actin disassembly. Genetic assays revealed that Abl allows growth factors and Semaphorin/Plexin repellents to combinatorially increase Mical-mediated F-actin disassembly, cellular remodeling, and repulsive axon guidance. Similar roles for Mical in growth factor/Abl-related cancer cell behaviors further revealed contexts in which characterized positive effectors of growth/guidance stimulate such negative cellular effects as F-actin disassembly/repulsion.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Gleevec; attraction; cytoskeleton; guidance cues; kinase; oxidation; phosphorylation; post-translational modification; redox enzyme; repulsion

Mesh:

Substances:

Year:  2017        PMID: 28689759      PMCID: PMC5564210          DOI: 10.1016/j.devcel.2017.06.007

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  74 in total

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5.  Phosphorylation of MICAL2 by ARG promotes head and neck cancer tumorigenesis by regulating skeletal rearrangement.

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