Differential Cellular Responses to Adhesive Interactions with Galectin-8 and Fibronectin Coated Substrates

The mechanisms underlying the cellular response to extracellular matrices (ECM), consisting of multiple adhesive ligands, are still poorly understood. Here we address this topic by monitoring the differential cellular response to two different extracellular adhesion molecules - fibronectin, a major...

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Detalles Bibliográficos
Autores: Li, Wenhong, Sancho Erkizia, Ana, Chung, Wen-Lu, Vinik, Yaron, Groll, Jürgen, Zick, Yehiel, Medalia, Ohad, Bershadsky, Alexander D., Geiger, Benjamin
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universidad del País Vasco
Repositorio:Addi. Archivo Digital para la Docencia y la Investigación
OAI Identifier:oai:addi.ehu.eus:10810/51217
Acceso en línea:http://hdl.handle.net/10810/51217
Access Level:acceso abierto
Palabra clave:extracellular matrix
filopodia
focal adhesions
lamellipodia
Myosin-II
Rho GTPases
Descripción
Sumario:The mechanisms underlying the cellular response to extracellular matrices (ECM), consisting of multiple adhesive ligands, are still poorly understood. Here we address this topic by monitoring the differential cellular response to two different extracellular adhesion molecules - fibronectin, a major integrin ligand, and galectin-8, a lectin, that binds beta-galactoside residues, as well as to mixtures of the two proteins. Cell spreading on galectin-8 coated substrates results in a larger projected cell area, a more extensive extension of filopodia, yet an inability to form focal adhesions and stress fibers, compared to cell spreading on fibronectin. These differences can be partially reversed by experimental manipulations of small G-proteins of the Rho family and their downstream targets, such as formins, Arp2/3 complex, and Rho kinase. We also show that the physical adhesion of cells to galectin-8 is stronger than the adhesion to fibronectin. Notably, galectin-8 and fibronectin differentially regulate cell spreading and focal adhesion formation, yet they act synergistically to upregulate the number and length of filopodia. The physiological significance of the coherent cellular response to a molecularly complex matrix is discussed