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骨形态发生蛋白配体 Gdf6 可防止颅早期发育中冠状缝间充质的分化。

The BMP ligand Gdf6 prevents differentiation of coronal suture mesenchyme in early cranial development.

机构信息

Department of Molecular Physiology and Biophysics, Center for Human Genetics Research, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.

出版信息

PLoS One. 2012;7(5):e36789. doi: 10.1371/journal.pone.0036789. Epub 2012 May 31.

Abstract

Growth Differentiation Factor-6 (Gdf6) is a member of the Bone Morphogenetic Protein (BMP) family of secreted signaling molecules. Previous studies have shown that Gdf6 plays a role in formation of a diverse subset of skeletal joints. In mice, loss of Gdf6 results in fusion of the coronal suture, the intramembranous joint that separates the frontal and parietal bones. Although the role of GDFs in the development of cartilaginous limb joints has been studied, limb joints are developmentally quite distinct from cranial sutures and how Gdf6 controls suture formation has remained unclear. In this study we show that coronal suture fusion in the Gdf6-/- mouse is due to accelerated differentiation of suture mesenchyme, prior to the onset of calvarial ossification. Gdf6 is expressed in the mouse frontal bone primordia from embryonic day (E) 10.5 through 12.5. In the Gdf6-/- embryo, the coronal suture fuses prematurely and concurrently with the initiation of osteogenesis in the cranial bones. Alkaline phosphatase (ALP) activity and Runx2 expression assays both showed that the suture width is reduced in Gdf6+/- embryos and is completely absent in Gdf6-/- embryos by E12.5. ALP activity is also increased in the suture mesenchyme of Gdf6+/- embryos compared to wild-type. This suggests Gdf6 delays differentiation of the mesenchyme occupying the suture, prior to the onset of ossification. Therefore, although BMPs are known to promote bone formation, Gdf6 plays an inhibitory role to prevent the osteogenic differentiation of the coronal suture mesenchyme.

摘要

生长分化因子-6(Gdf6)是骨形态发生蛋白(BMP)家族中一种分泌的信号分子。先前的研究表明,Gdf6 在形成多种骨骼关节中起作用。在小鼠中,Gdf6 的缺失导致冠状缝融合,即分离额骨和顶骨的膜内关节。尽管已经研究了 GDF 在软骨肢关节发育中的作用,但肢关节在发育上与颅缝有很大的不同,并且 Gdf6 如何控制缝的形成仍然不清楚。在这项研究中,我们表明 Gdf6-/- 小鼠冠状缝的融合是由于缝间质的分化加速,早于颅骨骨化的开始。Gdf6 从胚胎第 10.5 天到第 12.5 天在小鼠额骨原基中表达。在 Gdf6-/- 胚胎中,冠状缝过早融合,并与颅骨骨化同时发生。碱性磷酸酶(ALP)活性和 Runx2 表达测定均表明,Gdf6+/- 胚胎的缝宽度减小,并且在 E12.5 时 Gdf6-/- 胚胎的缝完全不存在。与野生型相比,Gdf6+/- 胚胎中的缝间质中的 ALP 活性也增加。这表明 Gdf6 延迟了占据缝的间质的分化,直到骨化开始。因此,尽管 BMP 已知可促进骨形成,但 Gdf6 发挥抑制作用,以防止冠状缝间质的成骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9cb/3365063/9403c5ce70d0/pone.0036789.g001.jpg

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