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首页> 外文期刊>Journal of Anatomy >An in situ hybridization study of Runx2, Osterix, and Sox9 at the onset of condylar cartilage formation in fetal mouse mandible.
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An in situ hybridization study of Runx2, Osterix, and Sox9 at the onset of condylar cartilage formation in fetal mouse mandible.

机译:胎儿小鼠下颌骨con突软骨形成开始时Runx2,Osterix和Sox9的原位杂交研究。

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摘要

Mandibular condylar cartilage is the principal secondary cartilage, differing from primary cartilage in its rapid differentiation from progenitor cells (preosteoblasts/skeletoblasts) to hypertrophic chondrocytes. The expression of three transcription factors related to bone and cartilage formation, namely Runx2, Osterix and Sox9, was investigated at the onset of mouse mandibular condylar cartilage formation by in situ hybridization. Messenger RNAs for these three molecules were expressed in the condylar anlage, consisting of preosteoblasts/skeletoblasts, at embryonic day (E)14. Hypertrophic chondrocytes appeared at E15 as soon as cartilage tissue appeared. Runx2 mRNA was expressed in the embryonic zone at the posterior position of the newly formed cartilage, in the bone collar and in the newly formed cartilage, but expression intensity in the newly formed cartilage was slightly weaker. Osterix mRNA was also expressed in the embryonic zone and in the bone collar, but was at markedly lower levels in the newly formed cartilage. Sox9 mRNA was continuously expressed from the embryonic zone to the newly formed cartilage. At this stage, Sox5 mRNA was expressed only in the newly formed cartilage. These results suggest that reduced expression of Osterix in combination with Sox9-Sox5 expression is important for the onset of condylar (secondary) cartilage formation.
机译:下颌con突软骨是主要的继发性软骨,与原发性软骨的区别在于其从祖细胞(前成骨细胞/成骨细胞)快速分化为肥大性软骨细胞。在小鼠下颌at突软骨形成开始时,通过原位杂交研究了与骨骼和软骨形成有关的三个转录因子Runx2,Osterix和Sox9的表达。这三个分子的信使RNA在胚胎天(E)14在in前突中表达,由前成骨细胞/成骨细胞组成。软骨组织出现后,E15处出现肥大的软骨细胞。 Runx2 mRNA在新形成的软骨的后部的胚胎区域,骨颈和新形成的软骨中表达,但是在新形成的软骨中的表达强度稍弱。 Osterix mRNA在胚胎区和骨环中也有表达,但在新形成的软骨中明显较低。 Sox9 mRNA从胚胎区域持续表达到新形成的软骨。在此阶段,Sox5 mRNA仅在新形成的软骨中表达。这些结果表明,Osterix的表达降低与Sox9-Sox5的表达结合对于con突(继发)软骨形成的发作很重要。

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