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Development of the articular cavity in the rat temporomandibular joint with special reference to the behavior of endothelial cells and macrophages

机译:大鼠颞下颌关节关节腔的发育,特别要注意内皮细胞和巨噬细胞的行为

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Previous developmental studies on the temporomandibular joint (TMJ) have proposed several hypotheses on the formation of its articular cavity. However, detailed information is meager. The present study examined the formation process of the articular cavity in the rat TMJ by immunocytochemistry for CD31, RECA-1, and ED1, which are useful cellular markers for endothelial cells and monocyte/macrophage lineages, respectively. The upper articular cavity formation had begun by embryonic day 21 (E21) and was completed at postnatal day 1 (P1) in advance of the lower cavitation; the latter took place from P1 to P3. The occurrence and distribution pattern of the CD31-, RECA-1-, and ED1-positive cells differed between the upper and lower articular cavity-forming areas: the ED1-positive cells exclusively occurred in the area of the prospective upper articular cavity prior to its formation, while no ED1-positive cell appeared in the lower cavity-forming area. In contrast, the CD31- and RECA-1-positive endothelial cells were restricted to the lower cavity-forming area (never the prospective upper cavity) at E19 and diminished thereafter. Throughout the cavity formation, we failed to find any apoptotic cells in the cavity formation area, indicating no involvement of apoptosis in the cavity formation in TMJ. The present findings on the behaviors of endothelial cells and ED1-positive cells show a possibility of different mechanism in the cavity formation between the upper and lower articular cavities in the rat TMJ. The appearance of ED1-reactive cells and temporal vascularization may play crucial roles in the upper and lower articular cavity formation, respectively. (C) 2005 Wiley-Liss, Inc.
机译:关于颞下颌关节(TMJ)的先前发展研究已经提出了关于其关节腔形成的几种假设。但是,详细信息很少。本研究通过免疫细胞化学对大鼠TMJ的CD31,RECA-1和ED1的免疫细胞化学进行了检查,这些CD31,RECA-1和ED1分别是内皮细胞和单核细胞/巨噬细胞谱系的有用细胞标记。上关节腔的形成在胚胎第21天(E21)开始,并在出生后的第1天(P1)在下部空化之前完成;后者发生在P1到P3。 CD31,RECA-1和ED1阳性细胞的发生和分布模式在上,下关节腔形成区域之间有所不同:ED1阳性细胞仅在前瞻性上关节腔区域发生其形成,而在下腔形成区域中没有ED1阳性细胞出现。相比之下,CD31和RECA-1阳性的内皮细胞在E19处被限制在下腔形成区域(绝非预期的上腔),并且此后减少。在整个腔形成过程中,我们未能在腔形成区域中找到任何凋亡细胞,这表明TMJ的腔形成中未涉及凋亡。目前关于内皮细胞和ED1阳性细胞行为的发现表明,在大鼠TMJ的上,下关节腔之间的腔形成中可能存在不同机制的可能性。 ED1反应性细胞的出现和颞血管形成可能分别在上,下关节腔的形成中起关键作用。 (C)2005 Wiley-Liss,Inc.

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