Literature DB >> 27135389

Cell adhesion and invasion mechanisms that guide developing axons.

Caitlin A Short1, Edwin A Suarez-Zayas1, Timothy M Gomez2.   

Abstract

Axon extension, guidance and tissue invasion share many similarities to normal cell migration and cancer cell metastasis. Proper cell and growth cone migration requires tightly regulated adhesion complex assembly and detachment from the extracellular matrix (ECM). In addition, many cell types actively remodel the ECM using matrix metalloproteases (MMPs) to control tissue invasion and cell dispersal. Targeting and activating MMPs is a tightly regulated process, that when dysregulated, can lead to cancer cell metastasis. Interestingly, new evidence suggests that growth cones express similar cellular and molecular machinery as migrating cells to clutch retrograde actin flow on ECM proteins and target matrix degradation, which may be used to facilitate axon pathfinding through the basal lamina and across tissues.
Copyright © 2016 Elsevier Ltd. All rights reserved.

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Year:  2016        PMID: 27135389      PMCID: PMC4987159          DOI: 10.1016/j.conb.2016.04.012

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  112 in total

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4.  Differential Regulation of Neurite Outgrowth and Growth Cone Morphology by 3D Fibronectin and Fibronectin-Collagen Extracellular Matrices.

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Review 7.  RACK1 regulates neural development.

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8.  Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration.

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