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Abstracts of papers presented at the 23rd Genetics Society's Mammalian Genetics and Development Workshop held at the Institute of Child Health, University College London on 22nd November 2012

机译:2012年11月22日在2012年11月22日在儿童健康研究所举行的23次遗传学协会哺乳动物遗传学和开发研讨会上提出的论文摘要

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摘要

The growth of the tooth and alveolar bone is coordinatedso that a studied distance always separatesthe two. We have called this distance, the tooth-boneinterface (TBI). Lack of mineralization, a crucial featureof the TBI, creates the space for the developingtooth to grow and the soft tissues of the periodontiumto develop. No studies have been done to understandthe signals that maintain the bone-free TBI, or theinfluence of the TBI on tooth development. We haveinvestigated the impact of the developing alveolarbone on the size and development of the mouse firstmolar (M1). We evaluated the growth and osteoclastsdistribution of the M1 in explant cultures using twomethods, isolation of the M1 from the surroundingalveolar bone, and enhancement of osteoclastogenesisthrough RANK-RANKL signalling after treatmentwith RANKL, an osteoclast activator. Both methodsshowed a significant increase in the size of M1. Ourdata indicate that alveolar bone and RANKL regulatetooth size without altering development and osteoclastsare indispensable in promoting theformation of the TBI. We intend to further investigatethe interactions between the tooth and alveolar boneduring development, looking at the roles of othergenes involved in TBI formation.
机译:牙齿和肺泡骨的生长是协调的,所以研究的距离总是分层。我们已叫这个距离,牙齿 - 骨质接口(TBI)。缺乏矿化,TBI的一个至关重要的特点,创造了呈现性的空间来生长,并且延期的软组织发展。没有进行研究以了解维持无骨TBI的信号,或TBI对牙齿发育的影响。我们已经投脑了发育肺泡对小鼠Firstmolar(M1)的大小和发育的影响。我们使用Twomethods评估了M1中M1中M1的生长和骨核算分布,从周围的骨骨中分离M1,并在治疗后,增强骨酮骨酮round rankl信号传导。两种方法都显着增加了M1的大小。 Ourdata表示肺泡骨和Rankl调节性,而不改变开发和骨核糖丸不可或缺在促进TBI的形态方面是必不可少的。我们打算进一步调查牙齿和肺泡骨髓发育之间的相互作用,观察参与TBI形成的其他作用。

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