Type V collagen exhibits distinct regulatory activities in TMJ articular disc versus condylar cartilage during postnatal growth and remodeling

被引:3
作者
Chandrasekaran, Prashant [1 ]
Alanazi, Abdulaziz [1 ]
Kwok, Bryan [1 ]
Li, Qing [1 ]
Viraraghavan, Girish [1 ]
Balasubramanian, Sriram [1 ]
Frank, David B. [2 ,3 ,4 ]
Lu, X. Lucas [5 ]
Birk, David E. [6 ]
Mauck, Robert L. [7 ,8 ]
Dyment, Nathaniel A. [7 ]
Koyama, Eiki [9 ]
Han, Lin [1 ]
机构
[1] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[2] Univ Penn, Penn CHOP Lung Biol Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Penn Cardiovasc Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Dept Pediat, Div Pediat Cardiol, Philadelphia, PA 19104 USA
[5] Univ Delaware, Dept Mech Engn, Newark, DE 19716 USA
[6] Univ S Florida, Morsani Sch Med, Dept Mol Pharmacol & Physiol, Tampa, FL 33612 USA
[7] Univ Penn, Perelman Sch Med, Dept Orthopaed Surg, McKay Orthopaed Res Lab, Philadelphia, PA 19104 USA
[8] Corporal Michael J Crescenz Vet Adm Med Ctr, Translat Musculoskeletal Res Ctr, Philadelphia, PA 19104 USA
[9] Childrens Hosp Philadelphia, Dept Surg, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Type V collagen; Temporomandibular joint; Fibrocartilage; Extracellular matrix; Mechanobiology; TEMPOROMANDIBULAR-JOINT DISC; EHLERS-DANLOS-SYNDROME; CELL; OSTEOARTHRITIS; DEGRADATION; DISORDERS; DEFICIENT; TURNOVER; MODEL; MICE;
D O I
10.1016/j.actbio.2024.09.046
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Understanding matrix molecular activities that regulate the postnatal growth and remodeling of the temporomandibular joint (TMJ) articular disc and condylar cartilage will enable the development of effective regenerative strategies targeting TMJ disorders. This study elucidated the distinct roles of type V collagen (collagen V) in regulating these two units. Studying the TMJ of young adult Col5a1+/- mice, we found that loss of collagen V resulted in substantial changes in the proliferation, clustering and density of progenitors in condylar cartilage, but did not have a major impact on disc cells that are more fibroblast-like. Although loss of collagen V led to thickened collagen fibrils with increased heterogeneity in the disc, there were no significant changes in local micromodulus, except for a reduction at the posterior end of the inferior side. Following the induction of aberrant occlusal loading by the unilateral anterior crossbite (UAC) procedure, both wild-type (WT) and Col5a1+/- condylar cartilage exhibited salient remodeling, and Col5a1+/- condyle developed more pronounced degeneration and tissue hypertrophy at the posterior end than the WT. In contrast, neither UAC nor collagen V deficiency induced marked changes in the morphology or biomechanical properties of the disc. Together, our findings highlight the distinct roles of collagen V in regulating these two units during postnatal growth and remodeling, emphasizing its more crucial role in condylar cartilage due to its impact on the highly mechanosensitive progenitors. These results provide the foundation for using collagen V to improve the regeneration of TMJ and the care of patients with TMJ disorders. Statement of significance Successful regeneration of the temporomandibular joint (TMJ) articular disc and condylar cartilage remains a significant challenge due to the limited understanding of matrix molecular activities that regulate the formation and remodeling of these tissues. This study demonstrates that collagen V plays distinct and critical roles in these processes. In condylar cartilage, collagen V is essential for regulating progenitor cell fate and maintaining matrix integrity. In the disc, collagen V also regulates fibril structure and local micromechanics, but has a limited impact on cell phenotype or its remodeling response. Our findings establish collagen V as a key component in maintaining the integrity of these two units, with a more crucial role in condylar cartilage due to its impact on progenitor cell activities. (c) 2024 The Author(s). Published by Elsevier Ltd on behalf of Acta Materialia Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:192 / 207
页数:16
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