Literature DB >> 34087208

Depletion of HP1α alters the mechanical properties of MCF7 nuclei.

Susav Pradhan1, Raoul Solomon2, Ankita Gangotra3, Gleb E Yakubov4, Geoff R Willmott5, Catherine P Whitby1, Tracy K Hale6, Martin A K Williams7.   

Abstract

Within the nucleus of the eukaryotic cell, DNA is partitioned into domains of highly condensed, transcriptionally silent heterochromatin and less condensed, transcriptionally active euchromatin. Heterochromatin protein 1α (HP1α) is an architectural protein that establishes and maintains heterochromatin, ensuring genome fidelity and nuclear integrity. Although the mechanical effects of changes in the relative amount of euchromatin and heterochromatin brought about by inhibiting chromatin-modifying enzymes have been studied previously, here we measure how the material properties of the nuclei are modified after the knockdown of HP1α. These studies were inspired by the observation that poorly invasive MCF7 breast cancer cells become more invasive after knockdown of HP1α expression and that, indeed, in many solid tumors the loss of HP1α correlates with the onset of tumor cell invasion. Atomic force microscopy (AFM), optical tweezers (OT), and techniques based on micropipette aspiration (MA) were each used to characterize the mechanical properties of nuclei extracted from HP1α knockdown or matched control MCF7 cells. Using AFM or OT to locally indent nuclei, those extracted from MCF7 HP1α knockdown cells were found to have apparent Young's moduli that were significantly lower than nuclei from MCF7 control cells, consistent with previous studies that assert heterochromatin plays a major role in governing the mechanical response in such experiments. In contrast, results from pipette-based techniques in the spirit of MA, in which the whole nuclei were deformed and aspirated into a conical pipette, showed considerably less variation between HP1α knockdown and control, consistent with previous studies reporting that it is predominantly the lamins in the nuclear envelope that determine the mechanical response to large whole-cell deformations. The differences in chromatin organization observed by various microscopy techniques between the MCF7 control and HP1α knockdown nuclei correlate well with the results of our measured mechanical responses and our hypotheses regarding their origin.
Copyright © 2021 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2021        PMID: 34087208      PMCID: PMC8390905          DOI: 10.1016/j.bpj.2021.05.017

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   3.699


  57 in total

Review 1.  Heterochromatin instability in cancer: from the Barr body to satellites and the nuclear periphery.

Authors:  Dawn M Carone; Jeanne B Lawrence
Journal:  Semin Cancer Biol       Date:  2012-06-18       Impact factor: 15.707

2.  Flow-induced hardening of endothelial nucleus as an intracellular stress-bearing organelle.

Authors:  Shinji Deguchi; Kenjiro Maeda; Toshiro Ohashi; Masaaki Sato
Journal:  J Biomech       Date:  2005-09       Impact factor: 2.712

3.  Heterochromatin protein 1 expression is reduced in human thyroid malignancy.

Authors:  Maria S Tretiakova; Sarah D Bond; David Wheeler; Alejandro Contreras; Masha Kocherginsky; Todd G Kroll; Tracy K Hale
Journal:  Lab Invest       Date:  2014-05-19       Impact factor: 5.662

4.  If cell mechanics can be described by elastic modulus: study of different models and probes used in indentation experiments.

Authors:  Nataliia Guz; Maxim Dokukin; Vivekanand Kalaparthi; Igor Sokolov
Journal:  Biophys J       Date:  2014-08-05       Impact factor: 4.033

5.  Histones H3/H4 form a tight complex with the inner nuclear membrane protein LBR and heterochromatin protein 1.

Authors:  H Polioudaki; N Kourmouli; V Drosou; A Bakou; P A Theodoropoulos; P B Singh; T Giannakouros; S D Georgatos
Journal:  EMBO Rep       Date:  2001-09-24       Impact factor: 8.807

6.  LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation.

Authors:  Irina Solovei; Audrey S Wang; Katharina Thanisch; Christine S Schmidt; Stefan Krebs; Monika Zwerger; Tatiana V Cohen; Didier Devys; Roland Foisner; Leo Peichl; Harald Herrmann; Helmut Blum; Dieter Engelkamp; Colin L Stewart; Heinrich Leonhardt; Boris Joffe
Journal:  Cell       Date:  2013-01-31       Impact factor: 41.582

7.  Directed targeting of chromatin to the nuclear lamina is mediated by chromatin state and A-type lamins.

Authors:  Jennifer C Harr; Teresa Romeo Luperchio; Xianrong Wong; Erez Cohen; Sarah J Wheelan; Karen L Reddy
Journal:  J Cell Biol       Date:  2015-01-05       Impact factor: 10.539

Review 8.  The nuclear envelope in genome organization, expression and stability.

Authors:  Karim Mekhail; Danesh Moazed
Journal:  Nat Rev Mol Cell Biol       Date:  2010-05       Impact factor: 94.444

9.  Single-molecule kinetic analysis of HP1-chromatin binding reveals a dynamic network of histone modification and DNA interactions.

Authors:  Louise C Bryan; Daniel R Weilandt; Andreas L Bachmann; Sinan Kilic; Carolin C Lechner; Pascal D Odermatt; Georg E Fantner; Sandrine Georgeon; Oliver Hantschel; Vassily Hatzimanikatis; Beat Fierz
Journal:  Nucleic Acids Res       Date:  2017-10-13       Impact factor: 16.971

10.  Correlating nuclear morphology and external force with combined atomic force microscopy and light sheet imaging separates roles of chromatin and lamin A/C in nuclear mechanics.

Authors:  Chad M Hobson; Megan Kern; E Timothy O'Brien; Andrew D Stephens; Michael R Falvo; Richard Superfine
Journal:  Mol Biol Cell       Date:  2020-04-08       Impact factor: 4.138

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  1 in total

Review 1.  A survey of physical methods for studying nuclear mechanics and mechanobiology.

Authors:  Chad M Hobson; Michael R Falvo; Richard Superfine
Journal:  APL Bioeng       Date:  2021-11-18
  1 in total

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