Seidel Ronald, Blumer Michael, Zaslansky Paul, Knötel David, Huber Daniel R, Weaver James C, Fratzl Peter, Omelon Sidney, Bertinetti Luca, Dean Mason N
Department Biomaterials, Max Planck Institute of Colloids & Interfaces, Potsdam, Germany.
Division of Clinical and Functional Anatomy, Medical University of Innsbruck, Innsbruck, Austria.
J Struct Biol. 2017 Apr;198(1):5-18. doi: 10.1016/j.jsb.2017.03.004. Epub 2017 Mar 9.
The cartilaginous endoskeletons of elasmobranchs (sharks and rays) are reinforced superficially by minute, mineralized tiles, called tesserae. Unlike the bony skeletons of other vertebrates, elasmobranch skeletons have limited healing capability and their tissues' mechanisms for avoiding damage or managing it when it does occur are largely unknown. Here we describe an aberrant type of mineralized elasmobranch skeletal tissue called endophytic masses (EPMs), which grow into the uncalcified cartilage of the skeleton, but exhibit a strikingly different morphology compared to tesserae and other elasmobranch calcified tissues. We use materials and biological tissue characterization techniques, including computed tomography, electron and light microscopy, X-ray and Raman spectroscopy and histology to characterize the morphology, ultrastructure and chemical composition of tesserae-associated EPMs in different elasmobranch species. EPMs appear to develop between and in intimate association with tesserae, but lack the lines of periodic growth and varying mineral density characteristic of tesserae. EPMs are mineral-dominated (high mineral and low organic content), comprised of birefringent bundles of large calcium phosphate crystals (likely brushite) aligned end to end in long strings. Both tesserae and EPMs appear to develop in a type-2 collagen-based matrix, but in contrast to tesserae, all chondrocytes embedded or in contact with EPMs are dead and mineralized. The differences outlined between EPMs and tesserae demonstrate them to be distinct tissues. We discuss several possible reasons for EPM development, including tissue reinforcement, repair, and disruptions of mineralization processes, within the context of elasmobranch skeletal biology as well as damage responses of other vertebrate mineralized tissues.
软骨鱼类(鲨鱼和鳐鱼)的软骨内骨骼表面由微小的矿化薄片强化,这些薄片称为嵌片。与其他脊椎动物的硬骨骨骼不同,软骨鱼类的骨骼愈合能力有限,其组织在避免损伤或损伤发生时进行处理的机制在很大程度上尚不清楚。在这里,我们描述了一种异常的矿化软骨鱼类骨骼组织,称为内生肿块(EPMs),它生长到骨骼的未钙化软骨中,但与嵌片和其他软骨鱼类钙化组织相比,呈现出截然不同的形态。我们使用包括计算机断层扫描、电子和光学显微镜、X射线和拉曼光谱以及组织学在内的材料和生物组织表征技术,来表征不同软骨鱼类物种中与嵌片相关的EPMs的形态、超微结构和化学成分。EPMs似乎在嵌片之间形成并与之紧密相连,但缺乏嵌片特有的周期性生长线和不同的矿物质密度特征。EPMs以矿物质为主(高矿物质含量和低有机含量),由大的磷酸钙晶体(可能是透钙磷石)的双折射束组成,这些晶体首尾相连排列成长串。嵌片和EPMs似乎都在基于Ⅱ型胶原蛋白的基质中形成,但与嵌片不同的是,所有嵌入EPMs或与之接触的软骨细胞都是死亡且矿化的。EPMs和嵌片之间概述的差异表明它们是不同的组织。我们在软骨鱼类骨骼生物学以及其他脊椎动物矿化组织的损伤反应背景下,讨论了EPMs形成的几种可能原因,包括组织强化、修复和矿化过程的破坏。