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Geometrically constrained cytoskeletal reorganisation modulates DNA nanostructures uptake

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F25%3A00618720" target="_blank" >RIV/68378271:_____/25:00618720 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11320/25:10513051 RIV/00023001:_____/25:00085381

  • Result on the web

    <a href="https://hdl.handle.net/11104/0365605" target="_blank" >https://hdl.handle.net/11104/0365605</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/D5TB00074B" target="_blank" >10.1039/D5TB00074B</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Geometrically constrained cytoskeletal reorganisation modulates DNA nanostructures uptake

  • Original language description

    DNA nanostructures (DNs) have gained popularity in various biomedical applications due to their unique properties, including structural programmability, ease of synthesis and functionalization, and low cytotoxicity. Effective utilization of DNs in biomedical applications requires a fundamental understanding of their interactions with living cells and the mechanics of cellular uptake. Current knowledge primarily focuses on how the physicochemical properties of DNs, such as mass, shape, size, and surface functionalization, affect uptake efficacy. However, the role of cellular mechanics and morphology in DN uptake remains largely unexplored. In this work, we show that cells subjected to geometric constraints remodel their actin cytoskeleton, resulting in differential mechanical force generation that facilitates DN uptake. The length, number, and orientation of F-actin fibers are influenced by these constraints, leading to distinct mechanophenotypes. Overall, DN uptake is governed by F-actin forces arising from filament reorganisation under geometric constraints. These results underscore the importance of actin dynamics in the cellular uptake of DNs and suggest that leveraging geometric constraints to induce specific cell morphology adaptations could enhance the uptake of therapeutically designed DNs.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10610 - Biophysics

Result continuities

  • Project

    <a href="/en/project/LUAUS24038" target="_blank" >LUAUS24038: Mechanical regulation of functionalized DNA nanostructures processing by hepatic cells</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Materials Chemistry B

  • ISSN

    2050-750X

  • e-ISSN

    2050-7518

  • Volume of the periodical

    13

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    17

  • Pages from-to

    2335-2351

  • UT code for WoS article

    001400865800001

  • EID of the result in the Scopus database

    2-s2.0-85215854455