4.8 Article

Predicting bulk mechanical properties of cellularized collagen gels using multiphoton microscopy

Journal

ACTA BIOMATERIALIA
Volume 6, Issue 12, Pages 4657-4665

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2010.07.004

Keywords

Collagen; Fibroblast; Second harmonic; Fluorescence; Mechanical properties

Funding

  1. National Heart, Lung, and Blood Institute [R01 HL067954, HL085339]
  2. National Institute of Biomedical Imaging and Bioengineering [F31 EB006677]
  3. ARCS Foundation
  4. National Institutes of Health under National Center for Research Resources [P41RR01192]
  5. Arnold and Mabel Beckman Foundation

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Cellularized collagen gels are a common model in tissue engineering, but the relationship between the microstructure and bulk mechanical properties is only partially understood. Multiphoton microscopy (MPM) is an ideal non-invasive tool for examining collagen microstructure, cellularity and crosslink content in these gels. In order to identify robust image parameters that characterize microstructural determinants of the bulk elastic modulus, we performed serial MPM and mechanical tests on acellular and cellularized (normal human lung fibroblasts) collagen hydrogels, before and after glutaraldehyde cross-linking. Following gel contraction over 16 days, cellularized collagen gel content approached that of native connective tissues (similar to 200 mg ml(-1)). Young's modulus (E) measurements from acellular collagen gels (range 0.5-12 kPa) exhibited a power-law concentration dependence (range 3-9 mg ml(-1)) with exponents from 2.1 to 2.2, similar to other semiflexible biopolymer networks such as fibrin and actin. In contrast, cellularized collagen gel stiffness (range 0.5-27 kPa) produced concentration-dependent exponents of 0.7 uncrosslinked and 1.1 crosslinked (range similar to 5-200 mg ml(-1)). The variation in E of cellularized collagen hydrogels can be explained by a power-law dependence on robust image parameters: either the second harmonic generation (SHG) and two-photon fluorescence (TPF) (matrix component) skewness (R-2 = 0.75, exponents of -1.0 and -0.6, respectively); or alternatively the SHG and TPF (matrix component) speckle contrast (R-2 = 0.83, exponents of -0.7 and -1.8, respectively). Image parameters based on the cellular component of TPF signal did not improve the fits. The concentration dependence of E suggests enhanced stress relaxation in cellularized vs. acellular gels. SHG and TPF image skewness and speckle contrast from cellularized collagen gels can predict E by capturing mechanically relevant information on collagen fiber, cell and crosslink density. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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