Abstract

Here we present a model capable of self-healing and explore its ability to resolve pathological alterations in biological tissue. We derive a simple analytic model consisting of an agent representing a cell that exhibits anabolic or catabolic activity, and which interacts with its tissue substrate according to tissue stiffness. When perturbed, this system returns toward a stable fixed point, a process corresponding to self-healing. We implemented this agent-substrate mechanism numerically on a hexagonal elastic network representing biological tissue. Agents, representing fibroblasts, were placed on the network and allowed to migrate around while they remodeled the network elements according to their activity which was determined by the stiffnesses of network elements that each agent encountered during its random walk. Initial injury to the network was simulated by increasing the stiffness of a single central network element above baseline. This system also exhibits a fixed point represented by the uniform baseline state. During the approach to the fixed point, interactions between the agents and the network create a transient spatially extended halo of stiffer network elements around the site of initial injury, which aids in overall injury repair. Non-equilibrium constraints generated by persistent injury prohibit the network to return to baseline and results in progressive stiffening, mimicking the development of fibrosis. Additionally, reducing anabolic or catabolic rates delay self-healing, reminiscent of aging. Our model thus embodies what may be the simplest set of attributes required of a spatiotemporal self-healing system, and so may help understand altered self-healing in chronic fibrotic diseases and aging.

Highlights

  • Self-healing is the ability for spontaneous repair following injury and is a critical homeostatic feature of biological systems that allows them to survive the rigors of life’s experiences for extended periods

  • The aim of this study was to investigate whether a computational model of cells communicating with their surrounding extracellular matrix (ECM) network is capable of exhibiting behavior consistent with biological self-healing

  • We formulated an analytic model of the essential feedback process required for self-healing, and implemented it computationally in an elastic network representing the ECM of biological tissues

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Summary

Introduction

Self-healing is the ability for spontaneous repair following injury and is a critical homeostatic feature of biological systems that allows them to survive the rigors of life’s experiences for extended periods. Biological self-healing involves a complex interplay between numerous cell types in the body (Carlson and Longaker, 2004; Vidmar et al, 2017), leading inexorably to complete resolution of whatever damage the injury caused (Mutsaers et al, 1997). Being able to harness the power of self-healing is of great importance for medicine, and it has even recently led to the bio-inspired development of artificial self-healing systems (Mutsaers et al, 1997; Hong et al, 2019). We still have a poor understanding of the essential components required of any system in order for it to exhibit the property of self-repair; how repair becomes dysregulated in a disease such as IPF remains a mystery

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