Division of Craniofacial Development and Tissue Biology, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.
Anat Sci Int. 2022 Mar;97(2):213-220. doi: 10.1007/s12565-021-00643-6. Epub 2021 Dec 2.
Meckel's cartilage is essential for the normal development of the mandible. The fate of the intermediate portion of Meckel's cartilage is unique as most of it disappears soon after birth except for the part that forms the sphenomandibular ligament. The mechanism of the disappearance of Meckel's cartilage is unknown; therefore, this study was designed to investigate the process of Meckel's cartilage degradation, focusing on cartilage matrix calcification and the appearance of chondroclasts. Developing mouse mandibles at embryonic days 15, 16, 17, and 18, and postnatal day 2 were processed for whole-mount staining with alcian blue and alizarin red. The mandibles on embryonic days 15, 16, 17, and 18 were fixed and embedded in paraffin. Adjacent sections were processed for von Kossa and tartrate-resistant acid phosphatase (TRAP) histochemistry and scanning electron microscopy/energy-dispersive X-ray spectrometry (SEM/EDS). Calcification and the element concentrations of calcium, phosphorus, and carbon were examined with von Kossa histochemistry and SEM/EDS. The involvement of chondroclasts was investigated using TRAP histochemistry. The results demonstrated that the intermediate portion of Meckel's cartilage is resorbed by chondroclasts after chondrocyte hypertrophy and cartilage matrix calcification and that the mineral concentration of calcified Meckel's cartilage is comparable to that of the surrounding bone. This study contributes to the understanding of the mechanism of Meckel's cartilage resorption and provides useful insights into the development of the mandible.
Meckel 软骨对于下颌骨的正常发育至关重要。 Meckel 软骨中间部分的命运是独特的,因为它在出生后不久就会消失,除了形成蝶下颌韧带的部分。 Meckel 软骨消失的机制尚不清楚;因此,本研究旨在研究 Meckel 软骨降解的过程,重点关注软骨基质钙化和破骨细胞的出现。对胚胎第 15、16、17 和 18 天以及出生后第 2 天的发育中小鼠下颌骨进行阿利新蓝和茜素红全染色。将胚胎第 15、16、17 和 18 天的下颌骨固定并嵌入石蜡中。对相邻切片进行 von Kossa 和抗酒石酸酸性磷酸酶(TRAP)组织化学和扫描电子显微镜/能谱分析(SEM/EDS)处理。通过 von Kossa 组织化学和 SEM/EDS 检查钙化和钙、磷、碳元素的浓度。使用 TRAP 组织化学研究破骨细胞的参与。结果表明, Meckel 软骨中间部分在软骨细胞肥大和软骨基质钙化后被破骨细胞吸收,钙化的 Meckel 软骨的矿物质浓度与周围骨相似。本研究有助于了解 Meckel 软骨吸收的机制,并为下颌骨发育提供了有用的见解。