Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells

Abstract Background Nanoparticles (NPs) can enter cells and cause cellular dysfunction. For example, reactive oxygen species generated by NPs can damage the cytoskeleton and impair cellular adhesion properties. Previously, we reported that cell spreading and protrusion structures such as lamellipodi...

Full description

Bibliographic Details
Main Authors: Abdurazak Aman Ketebo, Tae Hwan Shin, Myeongjun Jun, Gwang Lee, Sungsu Park
Format: Article
Language:English
Published: BMC 2020-11-01
Series:Journal of Nanobiotechnology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12951-020-00730-2
_version_ 1797999258833518592
author Abdurazak Aman Ketebo
Tae Hwan Shin
Myeongjun Jun
Gwang Lee
Sungsu Park
author_facet Abdurazak Aman Ketebo
Tae Hwan Shin
Myeongjun Jun
Gwang Lee
Sungsu Park
author_sort Abdurazak Aman Ketebo
collection DOAJ
description Abstract Background Nanoparticles (NPs) can enter cells and cause cellular dysfunction. For example, reactive oxygen species generated by NPs can damage the cytoskeleton and impair cellular adhesion properties. Previously, we reported that cell spreading and protrusion structures such as lamellipodia and filopodia was reduced when cells are treated with silica-coated magnetic nanoparticles incorporating rhodamine B isothiocyanate (MNPs@SiO2(RITC)), even at 0.1 μg/μL. These protruded structures are involved in a cell’s rigidity sensing, but how these NPs affect rigidity sensing is unknown. Results Here, we report that the rigidity sensing of human embryonic kidney (HEK293) cells was impaired even at 0.1 μg/μL of MNPs@SiO2(RITC). At this concentration, cells were unable to discern the stiffness difference between soft (5 kPa) and rigid (2 MPa) flat surfaces. The impairment of rigidity sensing was further supported by observing the disappearance of locally contracted elastomeric submicron pillars (900 nm in diameter, 2 μm in height, 24.21 nN/μm in stiffness k) under MNPs@SiO2(RITC) treated cells. A decrease in the phosphorylation of paxillin, which is involved in focal adhesion dynamics, may cause cells to be insensitive to stiffness differences when they are treated with MNPs@SiO2(RITC). Conclusions Our results suggest that NPs may impair the rigidity sensing of cells even at low concentrations, thereby affecting cell adhesion and spreading.
first_indexed 2024-04-11T11:00:41Z
format Article
id doaj.art-466b8516f6be4400a8c9b8a5b0349804
institution Directory Open Access Journal
issn 1477-3155
language English
last_indexed 2024-04-11T11:00:41Z
publishDate 2020-11-01
publisher BMC
record_format Article
series Journal of Nanobiotechnology
spelling doaj.art-466b8516f6be4400a8c9b8a5b03498042022-12-22T04:28:36ZengBMCJournal of Nanobiotechnology1477-31552020-11-0118111110.1186/s12951-020-00730-2Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cellsAbdurazak Aman Ketebo0Tae Hwan Shin1Myeongjun Jun2Gwang Lee3Sungsu Park4School of Mechanical Engineering, Sungkyunkwan UniversityDepartment of Physiology, Ajou University School of MedicineSchool of Mechanical Engineering, Sungkyunkwan UniversityDepartment of Physiology, Ajou University School of MedicineSchool of Mechanical Engineering, Sungkyunkwan UniversityAbstract Background Nanoparticles (NPs) can enter cells and cause cellular dysfunction. For example, reactive oxygen species generated by NPs can damage the cytoskeleton and impair cellular adhesion properties. Previously, we reported that cell spreading and protrusion structures such as lamellipodia and filopodia was reduced when cells are treated with silica-coated magnetic nanoparticles incorporating rhodamine B isothiocyanate (MNPs@SiO2(RITC)), even at 0.1 μg/μL. These protruded structures are involved in a cell’s rigidity sensing, but how these NPs affect rigidity sensing is unknown. Results Here, we report that the rigidity sensing of human embryonic kidney (HEK293) cells was impaired even at 0.1 μg/μL of MNPs@SiO2(RITC). At this concentration, cells were unable to discern the stiffness difference between soft (5 kPa) and rigid (2 MPa) flat surfaces. The impairment of rigidity sensing was further supported by observing the disappearance of locally contracted elastomeric submicron pillars (900 nm in diameter, 2 μm in height, 24.21 nN/μm in stiffness k) under MNPs@SiO2(RITC) treated cells. A decrease in the phosphorylation of paxillin, which is involved in focal adhesion dynamics, may cause cells to be insensitive to stiffness differences when they are treated with MNPs@SiO2(RITC). Conclusions Our results suggest that NPs may impair the rigidity sensing of cells even at low concentrations, thereby affecting cell adhesion and spreading.http://link.springer.com/article/10.1186/s12951-020-00730-2LamellipodiaFilopodiaRigidity sensingSilica-coated magnetic nanoparticlesTraction force
spellingShingle Abdurazak Aman Ketebo
Tae Hwan Shin
Myeongjun Jun
Gwang Lee
Sungsu Park
Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
Journal of Nanobiotechnology
Lamellipodia
Filopodia
Rigidity sensing
Silica-coated magnetic nanoparticles
Traction force
title Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
title_full Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
title_fullStr Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
title_full_unstemmed Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
title_short Effect of silica-coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
title_sort effect of silica coated magnetic nanoparticles on rigidity sensing of human embryonic kidney cells
topic Lamellipodia
Filopodia
Rigidity sensing
Silica-coated magnetic nanoparticles
Traction force
url http://link.springer.com/article/10.1186/s12951-020-00730-2
work_keys_str_mv AT abdurazakamanketebo effectofsilicacoatedmagneticnanoparticlesonrigiditysensingofhumanembryonickidneycells
AT taehwanshin effectofsilicacoatedmagneticnanoparticlesonrigiditysensingofhumanembryonickidneycells
AT myeongjunjun effectofsilicacoatedmagneticnanoparticlesonrigiditysensingofhumanembryonickidneycells
AT gwanglee effectofsilicacoatedmagneticnanoparticlesonrigiditysensingofhumanembryonickidneycells
AT sungsupark effectofsilicacoatedmagneticnanoparticlesonrigiditysensingofhumanembryonickidneycells