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Nanoneedle-Mediated Stimulation of Cell Mechanotransduction Machinery.
Hansel, Catherine S; Crowder, Spencer W; Cooper, Samuel; Gopal, Sahana; João Pardelha da Cruz, Maria; de Oliveira Martins, Leonardo; Keller, Debora; Rothery, Stephen; Becce, Michele; Cass, Anthony E G; Bakal, Chris; Chiappini, Ciro; Stevens, Molly M.
Afiliación
  • Cooper S; Chester Beatty Laboratories , Institute for Cancer Research , London SW3 6JB , U.K.
  • João Pardelha da Cruz M; Department of Bioengineering and Institute for Bioengineering and Biosciences , Instituto Superior Técnico, Universidade de Lisboa , 1649-004 Lisbon , Portugal.
  • Bakal C; Chester Beatty Laboratories , Institute for Cancer Research , London SW3 6JB , U.K.
ACS Nano ; 13(3): 2913-2926, 2019 03 26.
Article en En | MEDLINE | ID: mdl-30829469
Biomaterial substrates can be engineered to present topographical signals to cells which, through interactions between the material and active components of the cell membrane, regulate key cellular processes and guide cell fate decisions. However, targeting mechanoresponsive elements that reside within the intracellular domain is a concept that has only recently emerged. Here, we show that mesoporous silicon nanoneedle arrays interact simultaneously with the cell membrane, cytoskeleton, and nucleus of primary human cells, generating distinct responses at each of these cellular compartments. Specifically, nanoneedles inhibit focal adhesion maturation at the membrane, reduce tension in the cytoskeleton, and lead to remodeling of the nuclear envelope at sites of impingement. The combined changes in actin cytoskeleton assembly, expression and segregation of the nuclear lamina, and localization of Yes-associated protein (YAP) correlate differently from what is canonically observed upon stimulation at the cell membrane, revealing that biophysical cues directed to the intracellular space can generate heretofore unobserved mechanosensory responses. These findings highlight the ability of nanoneedles to study and direct the phenotype of large cell populations simultaneously, through biophysical interactions with multiple mechanoresponsive components.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Silicio / Mecanotransducción Celular / Nanoestructuras Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: ACS Nano Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Silicio / Mecanotransducción Celular / Nanoestructuras Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: ACS Nano Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos