4.6 Article

Heterogeneous elastic response of human lung microvascular endothelial cells to barrier modulating stimuli

Journal

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2013.03.006

Keywords

F-actin; Cell; AFM; FEM; Elasticity

Funding

  1. National Heart Lung Blood Institute NIH [P01 HL 58064, R01 HL 88144]
  2. National Institute on Drug Abuse (NIDA) [5R01DA025296-05, 5R01DA024871-15]

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In this study we employ atomic force microscopy, supported by finite element analysis and fluorescence microscopy, to characterize the elastic properties accompanying cytoskeletal structural rearrangements of lung microvascular endothelial cells in response to barrier altering stimuli. Statistical analysis of elasticity data obtained from multiple cells demonstrates a heterogeneous cellular elastic response to barrier-enhancing and barrier-disrupting agents; sphingosine 1-phosphate (S1P) and thrombin, respectively. A small but detectable (10%) increase in the average elastic modulus of all cells is observed for S1P, which is accompanied by a corresponding significant decrease in cell thickness. Variable effects of thrombin on these parameters were observed. To account for possible substrate effects in our elasticity analysis, we analyzed only the low-force sections of the force-displacement curves and utilized a finite-thickness correction to the Hertzian model. Our finite element analysis results substantiate this approach. The heterogeneous elastic behavior correlates with differential cytoskeletal rearrangements observed with fluorescence microscopy. (C) 2013 Elsevier Inc. All rights reserved.

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