Contractile dynamics change before morphological cues during florescence illumination

S. G. Knoll, W. W. Ahmed, M Taher A Saif

Research output: Contribution to journalArticle

Abstract

Illumination can have adverse effects on live cells. However, many experiments, e.g. traction force microscopy, rely on fluorescence microscopy. Current methods to assess undesired photo-induced cell changes rely on qualitative observation of changes in cell morphology. Here we utilize a quantitative technique to identify the effect of light on cell contractility prior to morphological changes. Fibroblasts were cultured on soft elastic hydrogels embedded with fluorescent beads. The adherent cells generated contractile forces that deform the substrate. Beads were used as fiducial markers to quantify the substrate deformation over time, which serves as a measure of cell force dynamics. We find that cells exposed to moderate fluorescence illumination (λ = 540-585 nm, I = 12.5 W/m2, duration = 60 s) exhibit rapid force relaxation. Strikingly, cells exhibit force relaxation after only 2 s of exposure, suggesting that photo-induced relaxation occurs nearly immediately. Evidence of photo-induced morphological changes were not observed for 15-30 min after illumination. Force relaxation and morphological changes were found to depend on wavelength and intensity of excitation light. This study demonstrates that changes in cell contractility reveal evidence of a photo-induced cell response long before any morphological cues.

Original languageEnglish (US)
Article number18513
JournalScientific Reports
Volume5
DOIs
StatePublished - Dec 22 2015

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Lighting
Cues
Fiducial Markers
Light
Hydrogels
Atomic Force Microscopy
Traction
Fluorescence Microscopy
Fibroblasts
Fluorescence
Observation

ASJC Scopus subject areas

  • General

Cite this

Contractile dynamics change before morphological cues during florescence illumination. / Knoll, S. G.; Ahmed, W. W.; Saif, M Taher A.

In: Scientific Reports, Vol. 5, 18513, 22.12.2015.

Research output: Contribution to journalArticle

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