Dorsal and ventral stimuli in sandwich-like microenvironments. Effect on cell differentiation

dc.contributor.authorBallester Beltrán, Josées_ES
dc.contributor.authorLebourg, Myriam Madeleinees_ES
dc.contributor.authorSalmerón Sánchez, Manueles_ES
dc.contributor.funderMinisterio de Educaciónes_ES
dc.contributor.funderEuropean Commission
dc.date.accessioned2014-05-14T08:01:48Z
dc.date.issued2013-06-27
dc.description.abstractWhile most of the in vivo extracellular matrices are 3D, most of the in vitro cultures are 2D--where only ventral adhesion is permitted--thus modifying cell behavior as a way to self-adaptation to this unnatural environment. We hypothesize that the excitation of dorsal receptors in cells already attached on a 2D surface (sandwich culture) could cover the gap between 2D and 3D cell-material interactions and result in a more physiological cell behavior. In this study we investigate the role of dorsal stimulation on myoblast differentiation within different poly(L-lactic acid) (PLLA) sandwich-like microenvironments, including plain material and aligned fibers. Enhanced cell differentiation levels were found for cells cultured with dorsal fibronectin-coated films. Seeking to understand the underlying mechanisms, experiments were carried out with (i) different types of dorsal stimuli (FN, albumin, FN after blocking the RGD integrin-binding site and activating dorsal cell integrin receptors), (ii) in the presence of an inhibitor of cell contractility, and (iii) increasing the frequency of culture medium changes to assess the effect of paracrine factors. Furthermore, FAK and integrin expressions, determined by Western blotting, revealed differences between cell sandwiches and 2D controls. Results show a stimuli-dependent response to dorsal excitation, proving that integrin outside-in signaling is involved in the enhanced cell differentiation. Due to their easiness and versatility, these sandwich-like systems are excellent candidates to get deeper insights into the study of 3D cell behavior and to direct cell fate within multilayer constructs.es_ES
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationBallester Beltrán, J.; Lebourg, MM.; Salmerón Sánchez, M. (2013). Dorsal and ventral stimuli in sandwich-like microenvironments. Effect on cell differentiation. Biotechnology and Bioengineering. 11:3048-3058. https://doi.org/10.1002/bit.24972es_ES
dc.description.referencesBajaj, P., Reddy, B., Millet, L., Wei, C., Zorlutuna, P., Bao, G., & Bashir, R. (2011). Patterning the differentiation of C2C12 skeletal myoblasts. Integrative Biology, 3(9), 897. doi:10.1039/c1ib00058fes_ES
dc.description.referencesBallester-Beltrán, J., Cantini, M., Lebourg, M., Rico, P., Moratal, D., García, A. J., & Salmerón-Sánchez, M. (2011). Effect of topological cues on material-driven fibronectin fibrillogenesis and cell differentiation. Journal of Materials Science: Materials in Medicine, 23(1), 195-204. doi:10.1007/s10856-011-4532-zes_ES
dc.description.referencesBallester-Beltrán, J., Lebourg, M., Rico, P., & Salmerón-Sánchez, M. (2012). Dorsal and Ventral Stimuli in Cell–Material Interactions: Effect on Cell Morphology. Biointerphases, 7(1), 39. doi:10.1007/s13758-012-0039-5es_ES
dc.description.referencesBelkin, A. M., Zhidkova, N. I., Balzac, F., Altruda, F., Tomatis, D., Maier, A., … Burridge, K. (1996). Beta 1D integrin displaces the beta 1A isoform in striated muscles: localization at junctional structures and signaling potential in nonmuscle cells. The Journal of Cell Biology, 132(1), 211-226. doi:10.1083/jcb.132.1.211es_ES
dc.description.referencesBennett, A. M. (1997). Regulation of Distinct Stages of Skeletal Muscle Differentiation by Mitogen-Activated Protein Kinases. Science, 278(5341), 1288-1291. doi:10.1126/science.278.5341.1288es_ES
dc.description.referencesBoonen, K. J. M., Langelaan, M. L. P., Polak, R. B., van der Schaft, D. W. J., Baaijens, F. P. T., & Post, M. J. (2010). Effects of a combined mechanical stimulation protocol: Value for skeletal muscle tissue engineering. Journal of Biomechanics, 43(8), 1514-1521. doi:10.1016/j.jbiomech.2010.01.039es_ES
dc.description.referencesChan, X. C. Y., McDermott, J. C., & Siu, K. W. M. (2007). Identification of Secreted Proteins during Skeletal Muscle Development. Journal of Proteome Research, 6(2), 698-710. doi:10.1021/pr060448kes_ES
dc.description.referencesCharest, J. L., García, A. J., & King, W. P. (2007). Myoblast alignment and differentiation on cell culture substrates with microscale topography and model chemistries. Biomaterials, 28(13), 2202-2210. doi:10.1016/j.biomaterials.2007.01.020es_ES
dc.description.referencesChatzizacharias, N. A., Kouraklis, G. P., & Theocharis, S. E. (2008). Disruption of FAK signaling: A side mechanism in cytotoxicity. Toxicology, 245(1-2), 1-10. doi:10.1016/j.tox.2007.12.003es_ES
dc.description.referencesChen, S.-E., Jin, B., & Li, Y.-P. (2007). TNF-α regulates myogenesis and muscle regeneration by activating p38 MAPK. American Journal of Physiology-Cell Physiology, 292(5), C1660-C1671. doi:10.1152/ajpcell.00486.2006es_ES
dc.description.referencesClegg, C. H., Linkhart, T. A., Olwin, B. B., & Hauschka, S. D. (1987). Growth factor control of skeletal muscle differentiation: commitment to terminal differentiation occurs in G1 phase and is repressed by fibroblast growth factor. The Journal of Cell Biology, 105(2), 949-956. doi:10.1083/jcb.105.2.949es_ES
dc.description.referencesClemente, C. F. M. Z., Corat, M. A. F., Saad, S. T. O., & Franchini, K. G. (2005). Differentiation of C2C12 myoblasts is critically regulated by FAK signaling. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 289(3), R862-R870. doi:10.1152/ajpregu.00348.2004es_ES
dc.description.referencesCukierman, E. (2001). Taking Cell-Matrix Adhesions to the Third Dimension. Science, 294(5547), 1708-1712. doi:10.1126/science.1064829es_ES
dc.description.referencesCukierman, E., Pankov, R., & Yamada, K. M. (2002). Cell interactions with three-dimensional matrices. Current Opinion in Cell Biology, 14(5), 633-640. doi:10.1016/s0955-0674(02)00364-2es_ES
dc.description.referencesHaba, G. D. L., Cooper, G. W., & Elting, V. (1966). HORMONAL REQUIREMENTS FOR MYOGENESIS OF STRIATED MUSCLE IN VITRO: INSULIN AND SOMATOTROPIN. Proceedings of the National Academy of Sciences, 56(6), 1719-1723. doi:10.1073/pnas.56.6.1719es_ES
dc.description.referencesDi Carlo, A., De Mori, R., Martelli, F., Pompilio, G., Capogrossi, M. C., & Germani, A. (2004). Hypoxia Inhibits Myogenic Differentiation through Accelerated MyoD Degradation. Journal of Biological Chemistry, 279(16), 16332-16338. doi:10.1074/jbc.m313931200es_ES
dc.description.referencesEngler, A. J., Sen, S., Sweeney, H. L., & Discher, D. E. (2006). Matrix Elasticity Directs Stem Cell Lineage Specification. Cell, 126(4), 677-689. doi:10.1016/j.cell.2006.06.044es_ES
dc.description.referencesEvinger-Hodges, M. J., Ewton, D. Z., Seifert, S. C., & Florini, J. R. (1982). Inhibition of myoblast differentiation in vitro by a protein isolated from liver cell medium. The Journal of Cell Biology, 93(2), 395-401. doi:10.1083/jcb.93.2.395es_ES
dc.description.referencesFlorini, J. R., & Magri, K. A. (1989). Effects of growth factors on myogenic differentiation. American Journal of Physiology-Cell Physiology, 256(4), C701-C711. doi:10.1152/ajpcell.1989.256.4.c701es_ES
dc.description.referencesFlorini, J. R., Ewton, D. Z., & Magri, K. A. (1991). Hormones, Growth Factors, and Myogenic Differentiation. Annual Review of Physiology, 53(1), 201-216. doi:10.1146/annurev.ph.53.030191.001221es_ES
dc.description.referencesGarcı́a, A. J., Vega, M. D., & Boettiger, D. (1999). Modulation of Cell Proliferation and Differentiation through Substrate-dependent Changes in Fibronectin Conformation. Molecular Biology of the Cell, 10(3), 785-798. doi:10.1091/mbc.10.3.785es_ES
dc.description.referencesHouse, M., Daniel, J., Elstad, K., Socrate, S., & Kaplan, D. L. (2012). Oxygen Tension and Formation of Cervical-Like Tissue in Two-Dimensional and Three-Dimensional Culture. Tissue Engineering Part A, 18(5-6), 499-507. doi:10.1089/ten.tea.2011.0309es_ES
dc.description.referencesHutmacher, D. W. (2010). Biomaterials offer cancer research the third dimension. Nature Materials, 9(2), 90-93. doi:10.1038/nmat2619es_ES
dc.description.referencesIngber, D. E. (2003). Tensegrity I. Cell structure and hierarchical systems biology. Journal of Cell Science, 116(7), 1157-1173. doi:10.1242/jcs.00359es_ES
dc.description.referencesIshii, I. (2001). Histological and functional analysis of vascular smooth muscle cells in a novel culture system with honeycomb-like structure. Atherosclerosis, 158(2), 377-384. doi:10.1016/s0021-9150(01)00461-0es_ES
dc.description.referencesKislinger, T., Gramolini, A. O., Pan, Y., Rahman, K., MacLennan, D. H., & Emili, A. (2005). Proteome Dynamics during C2C12 Myoblast Differentiation. Molecular & Cellular Proteomics, 4(7), 887-901. doi:10.1074/mcp.m400182-mcp200es_ES
dc.description.referencesLI, Y.-P., & SCHWARTZ, R. J. (2001). TNF-α regulates early differentiation of C2C12 myoblasts in an autocrine fashion. The FASEB Journal, 15(8), 1413-1415. doi:10.1096/fj.00-0632fjees_ES
dc.description.referencesLiu, H., Niu, A., Chen, S.-E., & Li, Y.-P. (2011). β3-Integrin mediates satellite cell differentiation in regenerating mouse muscle. The FASEB Journal, 25(6), 1914-1921. doi:10.1096/fj.10-170449es_ES
dc.description.referencesLutolf MP Hubbell JA 2005 47 55es_ES
dc.description.referencesMancini, A., Sirabella, D., Zhang, W., Yamazaki, H., Shirao, T., & Krauss, R. S. (2011). Regulation of myotube formation by the actin-binding factor drebrin. Skeletal Muscle, 1(1), 36. doi:10.1186/2044-5040-1-36es_ES
dc.description.referencesMeighan, C. M., & Schwarzbauer, J. E. (2008). Temporal and spatial regulation of integrins during development. Current Opinion in Cell Biology, 20(5), 520-524. doi:10.1016/j.ceb.2008.05.010es_ES
dc.description.referencesO'Connell B 2002 Oval Profile Plot. Research Services Branch, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke. Available from http://rsbweb.nih.gov/ij/plugins/oval-profile.htmles_ES
dc.description.referencesPECKHAM, M. (2008). Engineering a multi-nucleated myotube, the role of the actin cytoskeleton. Journal of Microscopy, 231(3), 486-493. doi:10.1111/j.1365-2818.2008.02061.xes_ES
dc.description.referencesQuach, N. L., & Rando, T. A. (2006). Focal adhesion kinase is essential for costamerogenesis in cultured skeletal muscle cells. Developmental Biology, 293(1), 38-52. doi:10.1016/j.ydbio.2005.12.040es_ES
dc.description.referencesRasband WS ImageJ U.S. National Institutes of Health, Bethesda, Maryland, USA http://imagej.nih.gov/ij/1997-2012es_ES
dc.description.referencesRen, K., Crouzier, T., Roy, C., & Picart, C. (2008). Polyelectrolyte Multilayer Films of Controlled Stiffness Modulate Myoblast Cell Differentiation. Advanced Functional Materials, 18(9), 1378-1389. doi:10.1002/adfm.200701297es_ES
dc.description.referencesRimann, M., & Graf-Hausner, U. (2012). Synthetic 3D multicellular systems for drug development. Current Opinion in Biotechnology, 23(5), 803-809. doi:10.1016/j.copbio.2012.01.011es_ES
dc.description.referencesSalmerón-Sánchez, M., Rico, P., Moratal, D., Lee, T. T., Schwarzbauer, J. E., & García, A. J. (2011). Role of material-driven fibronectin fibrillogenesis in cell differentiation. Biomaterials, 32(8), 2099-2105. doi:10.1016/j.biomaterials.2010.11.057es_ES
dc.description.referencesSastry, S. K., Lakonishok, M., Wu, S., Truong, T. Q., Huttenlocher, A., Turner, C. E., & Horwitz, A. F. (1999). Quantitative Changes in Integrin and Focal Adhesion Signaling Regulate Myoblast Cell Cycle Withdrawal. The Journal of Cell Biology, 144(6), 1295-1309. doi:10.1083/jcb.144.6.1295es_ES
dc.description.referencesSchlaepfer, D. D., Hanks, S. K., Hunter, T., & Geer, P. van der. (1994). Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase. Nature, 372(6508), 786-791. doi:10.1038/372786a0es_ES
dc.description.referencesSCHOEN, R. C., BENTLEY, K. L., & KLEBE, R. J. (1982). Monoclonal Antibody Against Human Fibronectin Which Inhibits Cell Attachment. Hybridoma, 1(2), 99-108. doi:10.1089/hyb.1.1982.1.99es_ES
dc.description.referencesSelinummi, J., Seppälä, J., Yli-Harja, O., & Puhakka, J. A. (2005). Software for quantification of labeled bacteria from digital microscope images by automated image analysis. BioTechniques, 39(6), 859-863. doi:10.2144/000112018es_ES
dc.description.referencesSmith, A. S. T., Passey, S., Greensmith, L., Mudera, V., & Lewis, M. P. (2012). Characterization and optimization of a simple, repeatable system for the long term in vitro culture of aligned myotubes in 3D. Journal of Cellular Biochemistry, 113(3), 1044-1053. doi:10.1002/jcb.23437es_ES
dc.description.referencesStreuli, C. H. (2008). Integrins and cell-fate determination. Journal of Cell Science, 122(2), 171-177. doi:10.1242/jcs.018945es_ES
dc.description.referencesTamada, Y., & Ikada, Y. (1993). Effect of Preadsorbed Proteins on Cell Adhesion to Polymer Surfaces. Journal of Colloid and Interface Science, 155(2), 334-339. doi:10.1006/jcis.1993.1044es_ES
dc.description.referencesTanaka, K., Sato, K., Yoshida, T., Fukuda, T., Hanamura, K., Kojima, N., … Watanabe, H. (2011). Evidence for cell density affecting C2C12 myogenesis: possible regulation of myogenesis by cell-cell communication. Muscle & Nerve, 44(6), 968-977. doi:10.1002/mus.22224es_ES
dc.description.referencesTse, J. R., & Engler, A. J. (2011). Stiffness Gradients Mimicking In Vivo Tissue Variation Regulate Mesenchymal Stem Cell Fate. PLoS ONE, 6(1), e15978. doi:10.1371/journal.pone.0015978es_ES
dc.description.referencesWakelam, M. J. (1985). The fusion of myoblasts. Biochemical Journal, 228(1), 1-12. doi:10.1042/bj2280001es_ES
dc.description.referencesWei, W.-C., Lin, H.-H., Shen, M.-R., & Tang, M.-J. (2008). Mechanosensing machinery for cells under low substratum rigidity. American Journal of Physiology-Cell Physiology, 295(6), C1579-C1589. doi:10.1152/ajpcell.00223.2008es_ES
dc.description.referencesWEISS, P. (1959). Cellular Dynamics. Reviews of Modern Physics, 31(1), 11-20. doi:10.1103/revmodphys.31.11es_ES
dc.description.referencesYamada, K. M., Pankov, R., & Cukierman, E. (2003). Dimensions and dynamics in integrin function. Brazilian Journal of Medical and Biological Research, 36(8), 959-966. doi:10.1590/s0100-879x2003000800001es_ES
dc.description.referencesZelzer, M., Albutt, D., Alexander, M. R., & Russell, N. A. (2011). The Role of Albumin and Fibronectin in the Adhesion of Fibroblasts to Plasma Polymer Surfaces. Plasma Processes and Polymers, 9(2), 149-156. doi:10.1002/ppap.201100054es_ES
dc.description.sponsorshipContract grant sponsor: ERC - 306990en_EN
dc.description.upvformatpfin3058es_ES
dc.description.upvformatpinicio3048es_ES
dc.description.volume11es_ES
dc.embargo.lift10000-01-01
dc.embargo.termsforeveres_ES
dc.identifier.doi10.1002/bit.24972
dc.identifier.issn0006-3592
dc.identifier.urihttps://riunet.upv.es/handle/10251/37462
dc.languageIngléses_ES
dc.publisherWileyes_ES
dc.relation.ispartofBiotechnology and Bioengineeringes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ME//AP2009-2326/ES/AP2009-2326/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/306990/EU/Material-driven Fibronectin Fibrillogenesis to Engineer Synergistic Growth Factor Microenvironments/en_EN
dc.relation.publisherversionhttp://dx.doi.org/10.1002/bit.24972es_ES
dc.relation.references10.1039/c1ib00058fes_ES
dc.relation.references10.1007/s10856-011-4532-zes_ES
dc.relation.references10.1007/s13758-012-0039-5es_ES
dc.relation.references10.1083/jcb.132.1.211es_ES
dc.relation.references10.1126/science.278.5341.1288es_ES
dc.relation.references10.1016/j.jbiomech.2010.01.039es_ES
dc.relation.references10.1021/pr060448kes_ES
dc.relation.references10.1016/j.biomaterials.2007.01.020es_ES
dc.relation.references10.1016/j.tox.2007.12.003es_ES
dc.relation.references10.1152/ajpcell.00486.2006es_ES
dc.relation.references10.1083/jcb.105.2.949es_ES
dc.relation.references10.1152/ajpregu.00348.2004es_ES
dc.relation.references10.1126/science.1064829es_ES
dc.relation.references10.1016/S0955-0674(02)00364-2es_ES
dc.relation.references10.1073/pnas.56.6.1719es_ES
dc.relation.references10.1074/jbc.M313931200es_ES
dc.relation.references10.1016/j.cell.2006.06.044es_ES
dc.relation.references10.1083/jcb.93.2.395es_ES
dc.relation.references10.1152/ajpcell.1989.256.4.C701es_ES
dc.relation.references10.1146/annurev.ph.53.030191.001221es_ES
dc.relation.references10.1091/mbc.10.3.785es_ES
dc.relation.references10.1089/ten.tea.2011.0309es_ES
dc.relation.references10.1038/nmat2619es_ES
dc.relation.references10.1242/jcs.00359es_ES
dc.relation.references10.1016/S0021-9150(01)00461-0es_ES
dc.relation.references10.1074/mcp.M400182-MCP200es_ES
dc.relation.references10.1096/fj.00-0632fjees_ES
dc.relation.references10.1096/fj.10-170449es_ES
dc.relation.references10.1038/nbt1055es_ES
dc.relation.references10.1186/2044-5040-1-36es_ES
dc.relation.references10.1016/j.ceb.2008.05.010es_ES
dc.relation.references10.1111/j.1365-2818.2008.02061.xes_ES
dc.relation.references10.1016/j.ydbio.2005.12.040es_ES
dc.relation.references10.1002/adfm.200701297es_ES
dc.relation.references10.1016/j.copbio.2012.01.011es_ES
dc.relation.references10.1016/j.biomaterials.2010.11.057es_ES
dc.relation.references10.1083/jcb.144.6.1295es_ES
dc.relation.references10.1038/372786a0es_ES
dc.relation.references10.1089/hyb.1.1982.1.99es_ES
dc.relation.references10.2144/000112018es_ES
dc.relation.references10.1002/jcb.23437es_ES
dc.relation.references10.1242/jcs.018945es_ES
dc.relation.references10.1006/jcis.1993.1044es_ES
dc.relation.references10.1002/mus.22224es_ES
dc.relation.references10.1371/journal.pone.0015978es_ES
dc.relation.references10.1042/bj2280001es_ES
dc.relation.references10.1152/ajpcell.00223.2008es_ES
dc.relation.references10.1103/RevModPhys.31.11es_ES
dc.relation.references10.1590/S0100-879X2003000800001es_ES
dc.relation.references10.1002/ppap.201100054es_ES
dc.relation.senia254589
dc.rightsReserva de todos los derechoses_ES
dc.rights.accessRightsAbiertoes_ES
dc.subject3D matrix adhesiones_ES
dc.subjectfibronectines_ES
dc.subjectmultilayerses_ES
dc.subjectmyoblastses_ES
dc.subject.classificationFISICA APLICADAes_ES
dc.subject.classificationTERMODINAMICA APLICADA (UPV)es_ES
dc.titleDorsal and ventral stimuli in sandwich-like microenvironments. Effect on cell differentiationes_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublication
upv.uuida8ff7980-de6f-4924-8752-58375b133c19es_ES

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