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Aggouras, A. N.

Publications and source records attributed to Aggouras, A. N..

2 recordsLinked to original sources

Intrinsic Repair Capacity of Resident Tendon Cells is Dependent on Hole Size in an Ex Vivo Model of Laser-Induced Microdamage

While it is generally accepted that tendon healing following widespread extracellular matrix trauma is limited, tenocytes are thought to have the capacity to repair small amounts of microdamage generated through activities of daily living. Despite this, few studies have directly studied the mechanisms governing this process. To address this, we developed a tunable in vitro model of extracellular matrix microdamage in live tendon explants that enables us to track both clearance of denatured collagen microdamage and closure of a micro-sized defect in the tendon matrix. The purpose of this study was to controllably induce varying levels of localized microdamage to the tendon explants and identify (1) if thresholds for healing exist and (2) whether repair mechanisms are dependent on initial damage size. We found that within three weeks, all tendon explants were able to clear damaged matrix to some extent regardless of the damage size. Interestingly, larger 5 mJ and 10 mJ injuries resulted in a more robust rate of damaged matrix clearance in the later weeks, while smaller injuries exhibited a more consistent rate that led to full clearance in two explants. Greater than 50% clearance of denatured collagen microdamage was typically associated with an accompanying closure of the ECM defect, suggesting a strong relationship between clearance and closure. Overall, our work demonstrates the power of our laser-induced microdamage model, which enables the direct visualization of microdamage responses. This model will be a powerful asset for investigating mechanisms of damage accumulation and/or healing, as well as identifying local tendon-specific factors that can be leveraged for therapeutics.

bioengineering↗

Aged Tendons Exhibit Altered Mechanisms of Strain-Dependent Extracellular Matrix Remodeling

Aging is a primary risk factor for degenerative tendon injuries, yet the etiology and progression of this degeneration is poorly understood. While aged tendons have innate cellular differences that support a reduced ability to maintain mechanical tissue homeostasis, the response of aged tendons to altered levels of mechanical loading has not yet been studied. To address this question, we subjected young and aged murine flexor tendon explants to various levels of in vitro tensile strain. We first compared the effect of static and cyclic strain on matrix remodeling in young tendons, finding that cyclic strain is optimal for studying remodeling in vitro. We then investigated the remodeling response of young and aged tendon explants after 7 days of varied mechanical stimulus (stress-deprivation, 1%, 3%, 5%, or 7% cyclic strain) via assessment of tissue composition, biosynthetic capacity, and degradation profiles. We hypothesized that aged tendons would show muted adaptive responses to changes in tensile strain and exhibit a shifted mechanical setpoint, at which the remodeling balance is optimal. Interestingly, we found 1% cyclic strain best maintains native physiology while promoting ECM turnover for both age groups. However, aged tendons display fewer strain-dependent changes, suggesting a reduced ability to adapt to altered levels of mechanical loading. This work has significant impact in understanding the regulation of tissue homeostasis in aged tendons, which can inform clinical rehabilitation strategies for treating elderly patients.

bioengineering↗