University of Illinois at Chicago, Department of Oral Biology, Chicago, United States of America.
Tokyo Dental College, Department of Fixed Prosthodontics, Tokyo, Japan.
PLoS One. 2019 Mar 21;14(3):e0214072. doi: 10.1371/journal.pone.0214072. eCollection 2019.
End stage temporomandibular joint osteoarthritis (TMJ-OA) is characterized by fibrillations, fissures, clefts, and erosion of the mandibular condylar cartilage. The goal of this study was to define changes in pericellular and interterritorial delineations of the extracellular matrix (ECM) that occur preceding and concurrent with the development of this end stage degeneration in a murine surgical instability model. Two-photon fluorescence (TPF) and second harmonic generation (SHG) microscopy was used to evaluate TMJ-OA mediated changes in the ECM. We illustrate that TPF/SHG microscopy reconstructs the three-dimensional network of key fibrillar and micro-fibrillar collagens altered during the progression of TMJ-OA. This method not only generates spatially distinct pericellular and interterritorial delineations of the ECM but distinguishes early and end stage TMJ-OA by signal organization, orientation, and composition. Early stage TMJ-OA at 4- and 8-weeks post-injury is characterized by two structurally distinct regions containing dense, large fiber collagens and superficial, small fiber collagens rich in types I, III, and VI collagen oriented along the mesiodistal axis of the condyle. At 8-weeks post-injury, type VI collagen is locally diminished on the central and medial condyle, but the type I/III rich superficial layer is still present. Twelve- and 16-weeks post-injury mandibular cartilage is characteristic of end-stage disease, with hypocellularity and fibrillations, fissures, and clefts in the articular layer that propagate along the mediolateral axis of the MCC. We hypothesize that the localized depletion of interterritorial and pericellular type VI collagen may signify an early marker for the transition from early to end stage TMJ-OA, influence the injury response of the tissue, and underlie patterns of degeneration that follow attritional modes of failure.
终末期颞下颌关节骨关节炎(TMJ-OA)的特征是下颌髁状突软骨的纤维颤动、裂隙、裂缝和侵蚀。本研究的目的是定义在一种小鼠手术不稳定模型中,在发生这种终末期退变之前和同时发生的细胞外基质(ECM)的细胞周和细胞间边界的变化。双光子荧光(TPF)和二次谐波产生(SHG)显微镜用于评估 TMJ-OA 介导的 ECM 变化。我们表明,TPF/SHG 显微镜重建了在 TMJ-OA 进展过程中改变的关键纤维状和微纤维状胶原的三维网络。这种方法不仅生成 ECM 的空间上不同的细胞周和细胞间边界,而且通过信号组织、方向和组成来区分早期和晚期 TMJ-OA。损伤后 4 周和 8 周的早期 TMJ-OA 具有两个结构上不同的区域,含有密集的大纤维胶原和富含 I 型、III 型和 VI 型胶原的浅层小纤维胶原,这些胶原沿着髁突的近远中轴排列。在损伤后 8 周,中央和内侧髁突的 VI 型胶原局部减少,但富含 I/III 型的浅层仍存在。损伤后 12 周和 16 周的下颌软骨是终末期疾病的特征,关节层出现细胞减少、纤维颤动、裂隙和裂缝,这些裂缝沿着髁突的内外侧轴传播。我们假设细胞间和细胞周 VI 型胶原的局部耗竭可能是从早期到晚期 TMJ-OA 过渡的早期标志物,影响组织的损伤反应,并为随后的退行性模式奠定基础。