Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/77868

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Campo DCValorIdioma
dc.contributor.authorGómez-Florit, Manuelpor
dc.contributor.authorLabrador-Rached, Claudia J.por
dc.contributor.authorDomingues, Rui Miguel Andradepor
dc.contributor.authorGomes, Manuela E.por
dc.date.accessioned2022-05-24T13:57:04Z-
dc.date.available2023-05-01T06:00:29Z-
dc.date.issued2022-04-
dc.date.submitted2022-05-
dc.identifier.citationGómez-Florit M., Labrador-Rached C. J., Domingues R. M. A., Gomes M. E. The tendon microenvironment: Engineered in vitro models to study cellular crosstalk, Advanced Drug Delivery Reviews, Vol. 185, pp. 114299, doi:10.1016/j.addr.2022.114299, 2022por
dc.identifier.issn0169-409Xpor
dc.identifier.urihttps://hdl.handle.net/1822/77868-
dc.description.abstractTendinopathy is a multi-faceted pathology characterized by alterations in tendon microstructure, cellularity and collagen composition. Challenged by the possibility of regenerating pathological or ruptured tendons, the healing mechanisms of this tissue have been widely researched over the past decades. However, so far, most of the cellular players and processes influencing tendon repair remain unknown, which emphasizes the need for developing relevant in vitro models enabling to study the complex multicellular crosstalk occurring in tendon microenvironments. In this review, we critically discuss the insights on the interaction between tenocytes and the other tendon resident cells that have been devised through different types of existing in vitro models. Building on the generated knowledge, we stress the need for advanced models able to mimic the hierarchical architecture, cellularity and physiological signaling of tendon niche under dynamic culture conditions, along with the recreation of the integrated gradients of its tissue interfaces. In a forward-looking vision of the field, we discuss how the convergence of multiple bioengineering technologies can be leveraged as potential platforms to develop the next generation of relevant in vitro models that can contribute for a deeper fundamental knowledge to develop more effective treatments.por
dc.description.sponsorshipThe authors acknowledge the European Union’s Horizon 2020 research and innovation program under European Research Council grant agreement 772817 and Twinning grant agreement no. 810850 – Achilles. Fundação para a Ciência e a Tecnologia (FCT) for project PTDC/NAN-MAT/30595/2017 and for CEE-CIND/01375/2017 (MGF) and 2020.03410.CEECIND (RMAD). Schematics in some figures were created with BioRender.com. The authors also want to acknowledge Mahwish Bakht (3B’s Research Group, University of Minho) for designing Fig. 1.por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FNAN-MAT%2F30595%2F2017/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F01375%2F2017%2FCP1458%2FCT0023/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 3ed/2020.03410.CEECIND%2FCP1600%2FCT0013/PTpor
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/772817/EU-
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/810850/EU-
dc.rightsopenAccesspor
dc.subject2D modelspor
dc.subject3D modelspor
dc.subjectRegenerative medicinepor
dc.subjectTendinopathypor
dc.subjectTendonpor
dc.subjectTissue engineeringpor
dc.subjectBioengineeringpor
dc.titleThe tendon microenvironment: engineered in vitro models to study cellular crosstalkeng
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://doi.org/10.1016/j.addr.2022.114299por
dc.commentshttp://3bs.uminho.pt/node/20761por
oaire.citationVolume185por
dc.date.updated2022-05-18T10:21:52Z-
dc.identifier.eissn1872-8294por
dc.identifier.doi10.1016/j.addr.2022.114299por
dc.identifier.pmid35436570por
dc.subject.wosScience & Technologypor
sdum.journalAdvanced Drug Delivery Reviewspor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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