Show simple item record

dc.contributor.authorHerráez Aguilar, Diego
dc.contributor.authorMadrazo, Elena
dc.contributor.authorLópez Menéndez, Horacio
dc.contributor.authorRamírez, Manuel
dc.contributor.authorMonroy, Francisco
dc.contributor.authorRedondo Muñoz, Javier
dc.date.accessioned2020-07-14T11:03:52Z
dc.date.available2020-07-14T11:03:52Z
dc.date.issued2020
dc.identifier.issn2045-2322spa
dc.identifier.urihttp://hdl.handle.net/10641/1951
dc.description.abstractThe nucleus is fundamentally composed by lamina and nuclear membranes that enclose the chromatin, nucleoskeletal components and suspending nucleoplasm. The functional connections of this network integrate external stimuli into cell signals, including physical forces to mechanical responses of the nucleus. Canonically, the morphological characteristics of the nucleus, as shape and size, have served for pathologists to stratify and diagnose cancer patients; however, novel biophysical techniques must exploit physical parameters to improve cancer diagnosis. By using multiple particle tracking (MPT) technique on chromatin granules, we designed a SURF (Speeded Up Robust Features)-based algorithm to study the mechanical properties of isolated nuclei and in living cells. We have determined the apparent shear stiffness, viscosity and optical density of the nucleus, and how the chromatin structure influences on these biophysical values. Moreover, we used our MPT-SURF analysis to study the apparent mechanical properties of isolated nuclei from patients of acute lymphoblastic leukemia. We found that leukemia cells exhibited mechanical differences compared to normal lymphocytes. Interestingly, isolated nuclei from high-risk leukemia cells showed increased viscosity than their counterparts from normal lymphocytes, whilst nuclei from relapsed-patient's cells presented higher density than those from normal lymphocytes or standard- and high-risk leukemia cells. Taken together, here we presented how MPT-SURF analysis of nuclear chromatin granules defines nuclear mechanical phenotypic features, which might be clinically relevant.spa
dc.language.isoengspa
dc.publisherScientifics Reportsspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleMultiple particle tracking analysis in isolated nuclei reveals the mechanical phenotype of leukemia cells.spa
dc.typearticlespa
dc.description.versionpost-printspa
dc.rights.accessRightsopenAccessspa
dc.description.extent1994 KBspa
dc.identifier.doi10.1038/s41598-020-63682-5spa
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-020-63682-5spa


Files in this item

FilesSizeFormatView
1.- Multiple particle tracking.pdf1.947MbPDFView/Open

This item appears in the following Collection(s)

Show simple item record

Atribución-NoComercial-SinDerivadas 3.0 España
Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 España