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    Binding of the chemokine CXCL12 alpha to its natural extracellular matrix ligand heparan sulfate enables myoblast adhesion and facilitates cell motility

    Year: 2017

    Journal: Biomaterials, Volume 123, APR, page 24–38

    Authors: Thakar, Dhruv; Dalonneau, Fabien; Migliorini, Elisa; Lortat-Jacob, Hugues; Boturyn, Didier; Albiges-Rizo, Corinne; Coche-Guerente, Liliane; Picart, Catherine; Richter, Ralf P.

    Keywords: Glycosaminoglycan; Chemokine; Cell adhesion and migration; Biomimetics; Bioactive surfaces; Extracellular matrix

    The chemokine CXCL12 alpha is a potent chemoattractant that guides the migration of muscle precursor cells (myoblasts) during myogenesis and muscle regeneration. To study how the molecular presentation of chemokines influences myoblast adhesion and motility, we designed multifunctional biomimetic surfaces as a tuneable signalling platform that enabled the response of myoblasts to selected extracellular cues to be studied in a well-defined environment. Using this platform, we demonstrate that CXCL12 alpha, when presented by its natural extracellular matrix ligand heparan sulfate (HS), enables the adhesion and spreading of myoblasts and facilitates their active migration. In contrast, myoblasts also adhered and spread on CXCL12 alpha that was quasi-irreversibly surface-bound in the absence of HS, but were essentially immotile. Moreover, co-presentation of the cyclic RGD peptide as integrin ligand along with HS-bound CXCL12 alpha led to enhanced spreading and motility, in a way that indicates cooperation between CXCR4 (the CXCL12 alpha receptor) and integrins (the RGD receptors). Our findings reveal the critical role of HS in CXCL12 alpha induced myoblast adhesion and migration. The biomimetic surfaces developed here hold promise for mechanistic studies of cellular responses to different presentations of biomolecules. They may be broadly applicable for dissecting the signalling pathways underlying receptor cross-talks, and thus may guide the development of novel biomaterials that promote highly specific cellular responses. (C) 2017 Elsevier Ltd. All rights reserved.
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