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Nano-topography: Quicksand for cell cycle progression?
Giannini, Marianna; Primerano, Chiara; Berger, Liron; Giannaccini, Martina; Wang, Zhigang; Landi, Elena; Cuschieri, Alfred; Dente, Luciana; Signore, Giovanni; Raffa, Vittoria.
Afiliação
  • Giannini M; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: marianna.giannini@sssup.it.
  • Primerano C; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: chiaraprim@gmail.com.
  • Berger L; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: lirberger@gmail.com.
  • Giannaccini M; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: martina.giannaccini@unipi.it.
  • Wang Z; Institute for Medical Science and Technology, University of Dundee, Dundee, United Kingdom. Electronic address: z.z.wang@dundee.ac.uk.
  • Landi E; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: elena.landi@unipi.it.
  • Cuschieri A; Institute for Medical Science and Technology, University of Dundee, Dundee, United Kingdom. Electronic address: a.cuschieri@dundee.ac.uk.
  • Dente L; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: luciana.dente@unipi.it.
  • Signore G; Center for Nanotechnology Innovation @NEST, Istituto Italiano di Tecnologia, Pisa, Italy; NEST, Scuola Normale Superiore, and Istituto Nanoscienze-CNR, Pisa, Italy. Electronic address: giovanni.signore@iit.it.
  • Raffa V; Department of Biology, Università di Pisa, Pisa, Italy. Electronic address: vittoria.raffa@unipi.it.
Nanomedicine ; 14(8): 2656-2665, 2018 11.
Article em En | MEDLINE | ID: mdl-30010000
The 3-D spatial and mechanical features of nano-topography can create alternative environments, which influence cellular response. In this paper, murine fibroblast cells were grown on surfaces characterized by protruding nanotubes. Cells cultured on such nano-structured surface exhibit stronger cellular adhesion compared to control groups, but despite the fact that stronger adhesion is generally believed to promote cell cycle progression, the time cells spend in G1 phase is doubled. This apparent contradiction is solved by confocal microscopy analysis, which shows that the nano-topography inhibits actin stress fiber formation. In turn, this impairs RhoA activation, which is required to suppress the inhibition of cell cycle progression imposed by p21/p27. This finding suggests that the generation of stress fibers, required to impose the homeostatic intracellular tension, rather than cell adhesion/spreading is the limiting factor for cell cycle progression. Indeed, nano-topography could represent a unique tool to inhibit proliferation in adherent well-spread cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adesão Celular / Ciclo Celular / Nanoestruturas / Fibroblastos Limite: Animals Idioma: En Revista: Nanomedicine Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adesão Celular / Ciclo Celular / Nanoestruturas / Fibroblastos Limite: Animals Idioma: En Revista: Nanomedicine Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2018 Tipo de documento: Article