Abstract

Loading in cartilage is supported primarily by fibrillar collagen, and damage will impair the function of the tissue, leading to pathologies such as osteoarthritis. Damage is initiated by two types of matrix metalloproteinases, collagenase and gelatinase, that cleave and denature the collagen fibrils in the tissue. Experimental and modeling studies have revealed insights into the individual contributions of these two types of MMPs, as well as the mechanical response of intact fibrils and fibrils that have experienced random surface degradation. However, no research has comprehensively examined the combined influences of collagenases and gelatinases on collagen degradation nor studied the mechanical consequences of biological degradation of collagen fibrils. Such preclinical examinations are required to gain insights into understanding, treating, and preventing degradation-related cartilage pathology. To develop these insights, we use sequential Monte Carlo and molecular dynamics simulations to probe the effect of enzymatic degradation on the structure and mechanics of a single collagen fibril. We find that the mechanical response depends on the ratio of collagenase to gelatinase—not just the amount of lost fibril mass—and we provide a possible mechanism underlying this phenomenon. Overall, by characterizing the combined influences of collagenases and gelatinases on fibril degradation and mechanics at the preclinical research stage, we gain insights that may facilitate the development of targeted interventions to prevent the damage and loss of mechanical integrity that can lead to cartilage pathology.

Highlights

  • In healthy tissue, collagen production is typically balanced by collagen degradation mediated by matrix metalloproteinases (MMPs), enzymes that bind and cleave the triple helical collagen molecule

  • We developed a Metropolis Monte Carlo (MC) approach to examine the process of biological degradation of a collagen fibril by collagenase MMP-1 and gelatinase MMP-9

  • Our results demonstrate that the ratio of collagenase to gelatinase dictates fibril degradation and mechanical integrity

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Summary

Introduction

Collagen production is typically balanced by collagen degradation mediated by matrix metalloproteinases (MMPs), enzymes that bind and cleave the triple helical collagen molecule. This balance is disrupted in many disease states, including arthritis, cancer, and fibrosis (Cawston and Wilson 2006; Clark et al 2008; Giannandrea and Parks 2014; Malemud 2006; Mancini and Di Battista 2006). The balance favors destruction, permanent structural changes can occur, especially in tissues that are metabolically mostly quiescent, such as articular cartilage (Maroudas et al 1992; Verzijl et al 2000) Such damage can lead to changes in mechanical properties that impair the function of the tissue. While the isolated interactions of MMPs with their substrates have been experimentally characterized, the combined influences of collagenase and gelatinase on the structural and mechanical properties of an isolated collagen fibril have not been established

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