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. 2010 Dec;9(6):689-702.
doi: 10.1007/s10237-010-0205-y. Epub 2010 Mar 18.

Multigenerational interstitial growth of biological tissues

Affiliations

Multigenerational interstitial growth of biological tissues

Gerard A Ateshian et al. Biomech Model Mechanobiol. 2010 Dec.

Abstract

This study formulates a theory for multigenerational interstitial growth of biological tissues whereby each generation has a distinct reference configuration determined at the time of its deposition. In this model, the solid matrix of a growing tissue consists of a multiplicity of intermingled porous permeable bodies, each of which represents a generation, all of which are constrained to move together in the current configuration. Each generation's reference configuration has a one-to-one mapping with the master reference configuration, which is typically that of the first generation. This mapping is postulated based on a constitutive assumption with regard to that generations' state of stress at the time of its deposition. For example, the newly deposited generation may be assumed to be in a stress-free state, even though the underlying tissue is in a loaded configuration. The mass content of each generation may vary over time as a result of growth or degradation, thereby altering the material properties of the tissue. A finite element implementation of this framework is used to provide several illustrative examples, including interstitial growth by cell division followed by matrix turnover.

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Figures

Fig. 1
Fig. 1
Growth of a cantilever beam. a Stress-free reference configuration of T1 (first generation). b Loaded configuration of T1, also loaded configuration of T2, following growth of second generation. c Unloaded (residually stressed) configuration of T2
Fig. 2
Fig. 2
Effective normal stress distribution Txx at fixed end of cantilever beam
Fig. 3
Fig. 3
Thick-walled tube, growth in inner rim only; due to symmetry, only the right side of the tube is modeled. a T1 in stress-free configuration. b T1 (and T2) with internal pressurization. c T2 in unloaded configuration. d T2 in unloaded configuration, after radial cut; the opening angle is positive
Fig. 4
Fig. 4
Thick-walled tube, growth in outer rim only. a T1 in stress-free configuration. b T1 (and T2) with internal pressurization. c T2 in unloaded configuration. d T2 in unloaded configuration, after radial cut; the opening angle is negative
Fig. 5
Fig. 5
Thick-walled tube, homogeneous growth. a T1 in stress-free configuration. b T1 (and T2) with internal pressurization. c T2 in unloaded configuration. d T2 in unloaded configuration, after radial cut; the opening angle is negative
Fig. 6
Fig. 6
Radial distribution of residual circumferential normal effective stress at apex (Θ = π/2), for thick-walled tube in its second generation (T2) unloaded configuration, before and after radial cut. a Inner rim growth; b outer rim growth; c homogeneous growth
Fig. 7
Fig. 7
Growth by cell division, followed by matrix turnover. Js indicates the relative change in volume of T over time; p is the interstitial fluid pressure

References

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