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Expression and localization of insulin-like growth factor-I in four parts of the red deer antler.

机译:胰岛素样生长因子-I在马鹿茸的四个部分中的表达和定位。

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The expression and localization of insulin-like growth factor-I (IGF-I) in the four parts (tip, upper, mid and base) of the red deer antler has been extensively investigated. We used reverse transcriptase polymerase chain reaction (RT-PCR) and real-time reverse transcriptase polymerase chain reaction (real time RT-PCR), in situ hybridization, immunohistochemistry and Western blot techniques to localize IGF-I messenger ribonucleic acid (mRNA) and IGF-I peptide in the four parts of the antler. The specific sequence encoding IGF-I was detected by RT-PCR in all of the four specimens, and the 395 bp IGF-I sequence from the red deer antler was shown to have very high homology with human, goat and mouse IGF-I. In situ hybridization and immunohistochemistry results demonstrated that the expression of IGF-I occurred in chondrocytes and osteoblasts in the tip and upper parts of the antler. However, IGF-I was only detectable in osteoblasts around the bone in the mid and base parts. There were significant differences in the intensity of the signal obtained with the IGF-I probe in the tip, upper, mid and base tissues. The Western blot analysis also provided evidence that IGF-I expression was localized differentially in the four parts of the deer antler. This study indicates that antler tissue is an essential part of the IGF system, which is involved in the regulation of the growth of red deer antlers. The specific expression of IGF-I in the four parts of the deer antler suggests that the IGF-I molecule is present at significantly different levels throughout the deer antler development and regeneration processes. Localization of IGF-I in chondrocytes and osteoblasts suggests that IGF-I may play an important role in cartilage and bone formation. In addition, it may have a variety of biophysical effects that influence the rapid growth of deer antlers.
机译:胰岛素样生长因子-I(IGF-I)在马鹿茸的四个部分(尖端,上部,中部和底部)的表达和定位已得到广泛研究。我们使用逆转录聚合酶链反应(RT-PCR)和实时逆转录聚合酶链反应(实时RT-PCR),原位杂交,免疫组化和Western blot技术来定位IGF-1信使核糖核酸(mRNA)和IGF-1肽在鹿角的四个部分。通过RT-PCR在所有四个标本中检测到编码IGF-I的特异性序列,并且显示来自马鹿鹿角的395bp IGF-I序列与人,山羊和小鼠IGF-I具有非常高的同源性。原位杂交和免疫组化结果表明,IGF-I的表达发生在鹿角尖端和上部的软骨细胞和成骨细胞中。但是,仅在中部和基部的骨周围成骨细胞中检测到了IGF-I。使用IGF-I探针在尖端,上,中和基础组织中获得的信号强度存在显着差异。 Western印迹分析还提供了证据,即IGF-1表达差异地定位在鹿角的四个部分中。这项研究表明,鹿角组织是IGF系统的重要组成部分,它参与了对马鹿鹿角生长的调节。在鹿茸的四个部分中IGF-1的特异性表达表明,在整个鹿茸的发育和再生过程中,IGF-1分子以明显不同的水平存在。 IGF-1在软骨细胞和成骨细胞中的定位表明IGF-1可能在软骨和骨形成中起重要作用。另外,它可能具有影响鹿角快速生长的多种生物物理作用。

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