A. Saalbach , M. Stein , S. Lee , U. Krügel , M. Haffner-Luntzer , K. Krohn , S. Franz , J.C. Simon , J. Tuckermann , U. Anderegg
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We therefore investigated whether HA synthesis is involved in adult bone turnover and whether abrogation of HA synthesis in adult mice would alter bone quality.</div><div>To achieve complete abrogation of HA synthesis in adult mice, we generated a novel Has-total knockout (Has-tKO) mouse model in which a constitutive knockout of Has1 and Has3 was combined with an inducible, Ubc-Cre-driven Has2 knockout.</div><div>By comparing bone tissue from wild-type, Has1,3 double knockout and Has-tKO mice, we demonstrate that Has2-derived HA mainly contributes to the HA content in bone. Furthermore, Has-tKO mice show a significant decrease of bone integrity in trabecular and cortical bone, as shown by µ-CT analysis. These effects are detectable as early as five weeks after induced Has2 deletion, irrespective of sex and progress with age.</div><div>Mesenchymal stem cells (MSC) during osteogenic differentiation <em>in vitro</em> showed that Has2 expression is increased while Has3 expression is decreased during differentiation. Furthermore, the complete abrogation of HA synthesis results in significantly reduced osteogenic differentiation as indicated by reduced marker gene expression (Runx-2, Tnalp, Osterix) as well as alizarin red staining. RNAseq analysis revealed that MSC from Has-tKO are characterised by decreased expression of genes annotated for bone and organ development, whereas expression of genes associated with chemokine related interactions and cytokine signalling is increased.</div><div>Taken together, we present a novel mouse model with complete deletion of HA synthases in adult mice which has the potential to study HA function in different organs and during age-related HA reduction. 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Hyaluronan (HA) is an important glycosaminoglycan in many tissues including bone.</div><div>Previously, the importance of HA synthesis for bone development during embryogenesis has been shown. We therefore investigated whether HA synthesis is involved in adult bone turnover and whether abrogation of HA synthesis in adult mice would alter bone quality.</div><div>To achieve complete abrogation of HA synthesis in adult mice, we generated a novel Has-total knockout (Has-tKO) mouse model in which a constitutive knockout of Has1 and Has3 was combined with an inducible, Ubc-Cre-driven Has2 knockout.</div><div>By comparing bone tissue from wild-type, Has1,3 double knockout and Has-tKO mice, we demonstrate that Has2-derived HA mainly contributes to the HA content in bone. Furthermore, Has-tKO mice show a significant decrease of bone integrity in trabecular and cortical bone, as shown by µ-CT analysis. These effects are detectable as early as five weeks after induced Has2 deletion, irrespective of sex and progress with age.</div><div>Mesenchymal stem cells (MSC) during osteogenic differentiation <em>in vitro</em> showed that Has2 expression is increased while Has3 expression is decreased during differentiation. Furthermore, the complete abrogation of HA synthesis results in significantly reduced osteogenic differentiation as indicated by reduced marker gene expression (Runx-2, Tnalp, Osterix) as well as alizarin red staining. RNAseq analysis revealed that MSC from Has-tKO are characterised by decreased expression of genes annotated for bone and organ development, whereas expression of genes associated with chemokine related interactions and cytokine signalling is increased.</div><div>Taken together, we present a novel mouse model with complete deletion of HA synthases in adult mice which has the potential to study HA function in different organs and during age-related HA reduction. 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引用次数: 0
摘要
骨骼由复杂的矿化基质组成,通过不同类型细胞的合成和吸收控制平衡来维持。透明质酸(HA)是包括骨骼在内的许多组织中的一种重要的糖胺聚糖。因此,我们研究了 HA 合成是否参与了成年小鼠的骨转换,以及在成年小鼠中终止 HA 合成是否会改变骨质量。为了在成年小鼠中实现 HA 合成的完全终止,我们产生了一种新型的 Has-total knockout(Has-tKO)小鼠模型,在该模型中,Has1 和 Has3 的组成型基因敲除与 Ubc-Cre 驱动的诱导型 Has2 基因敲除相结合。通过比较野生型小鼠、Has1,3双基因敲除小鼠和Has-tKO小鼠的骨组织,我们证明Has2衍生的HA是骨中HA含量的主要来源。此外,µ-CT 分析显示,Has-tKO 小鼠骨小梁和骨皮质的骨完整性显著下降。间充质干细胞(MSC)在体外成骨分化过程中显示,分化过程中Has2表达增加,而Has3表达减少。此外,标记基因(Runx-2、Tnalp、Osterix)表达减少以及茜素红染色显示,完全终止HA合成会导致成骨分化明显降低。RNAseq分析表明,来自Has-tKO的间充质干细胞的特点是骨骼和器官发育基因表达减少,而与趋化因子相关的相互作用和细胞因子信号相关的基因表达增加。在骨骼方面,HA 合成对维持骨骼完整性非常重要,这可能是基于 HA 对成骨分化的强大作用。
Bone quality relies on hyaluronan synthesis – Insights from mice with complete knockout of hyaluronan synthase expression
Bone consists of a complex mineralised matrix that is maintained by a controlled equilibrium of synthesis and resorption by different cell types. Hyaluronan (HA) is an important glycosaminoglycan in many tissues including bone.
Previously, the importance of HA synthesis for bone development during embryogenesis has been shown. We therefore investigated whether HA synthesis is involved in adult bone turnover and whether abrogation of HA synthesis in adult mice would alter bone quality.
To achieve complete abrogation of HA synthesis in adult mice, we generated a novel Has-total knockout (Has-tKO) mouse model in which a constitutive knockout of Has1 and Has3 was combined with an inducible, Ubc-Cre-driven Has2 knockout.
By comparing bone tissue from wild-type, Has1,3 double knockout and Has-tKO mice, we demonstrate that Has2-derived HA mainly contributes to the HA content in bone. Furthermore, Has-tKO mice show a significant decrease of bone integrity in trabecular and cortical bone, as shown by µ-CT analysis. These effects are detectable as early as five weeks after induced Has2 deletion, irrespective of sex and progress with age.
Mesenchymal stem cells (MSC) during osteogenic differentiation in vitro showed that Has2 expression is increased while Has3 expression is decreased during differentiation. Furthermore, the complete abrogation of HA synthesis results in significantly reduced osteogenic differentiation as indicated by reduced marker gene expression (Runx-2, Tnalp, Osterix) as well as alizarin red staining. RNAseq analysis revealed that MSC from Has-tKO are characterised by decreased expression of genes annotated for bone and organ development, whereas expression of genes associated with chemokine related interactions and cytokine signalling is increased.
Taken together, we present a novel mouse model with complete deletion of HA synthases in adult mice which has the potential to study HA function in different organs and during age-related HA reduction. With respect to bone, HA synthesis is important for maintaining bone integrity, presumably based on the strong effect of HA on osteogenic differentiation.