Transcriptional Regulation of Indian Hedgehog Expression in Chondrocytes

软骨细胞中 Indian Hedgehog 表达的转录调控

• 批准号: 8277416
• 负责人: XIANGLI YANG
• 金额: $ 32.1万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-15 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8277416
• 关键词: Address; Agonist; BMP2 gene; Binding; Biochemical; Biological; Biological Assay; Biology; Bone Regeneration; CREB1 gene; Cartilage; Chondrocytes; Chondrogenesis; Coffin-Lowry syndrome; Defect; Degenerative polyarthritis; Disease; Elements; Epiphysial cartilage; Erinaceidae; Family; Fracture; Gene Expression; Gene Targeting; Genetic; Genetic Transcription; Human; Hypertrophy; Impairment; In Vitro; Investigation; Leucine Zippers; Limb Development; Limb structure; Link; Mental Retardation; Molecular; Molecular Genetics; Mus; Mutant Strains Mice; Mutate; Nuclear Extract; Organ Culture Techniques; Osteogenesis; Parathyroid Hormone Receptor; Pathway interactions; Phenotype; Phosphorylation; Process; Protein Kinase; Proteins; Regulation; Role; Skeletal Development; Skeletal bone; Staging; System; Testing; Transactivation; Transcriptional Regulation; Transgenic Mice; Vascular Endothelial Growth Factors; Yang; base; improved; in utero; in vivo; mineralization; morphogens; mouse model; novel; osteoblast differentiation; overexpression; parathyroid hormone-related protein; premature; promoter; purmorphamine; receptor; repaired; skeletal; smoothened signaling pathway; transcription factor

PROJECT SUMMARY/ABSTRACT During endochondral bone formation, osteogenesis and chondrogenesis are linked and highly coordinated. However, the regulatory mechanisms responsible for coordinating osteogenesis and chondrogenesis remain unclear. Genetic mouse models have shown that the Hedgehog (Hh) pathway, which controls target genes in chondrogenesis such as PTHrP and osteogenesis such as BMP2, is essential for normal endochondral bone formation. However, despite its obvious importance, little is known of the regulatory mechanisms that are responsible for controlling Hedgehog signaling. This proposal is directed at improving understanding of the transcriptional control of the Hedgehog pathway, and specifically of Ihh, during chondrogenesis and how it may be linked to osteogenesis. Since chondrocyte differentiation occurs also at early stages of cartilage degeneration as well as during bone regeneration, this study is directly applicable to diseases such as osteoarthritis and fractures. We hypothesize that the transcription factor ATF4 is a major regulator of Hedgehog signaling during chondrogenesis, and possibly during osteogenesis as well. Further, we hypothesize that ATF4 is a direct regulator of Ihh transcription. We base this hypothesis on the following rationale. 1. We have found that ATF4 is essential for osteoblast differentiation and bone formation (Yang, et al., 2004). 2. Atf4-deficient (Atf4-/-) mice are dwarfs, suggesting a defect in growth plate chondrocytes. 3. Atf4-/- growth plate chondrocytes show several abnormalities including a delay in hypertrophic mineralization, an expansion of the hypertrophic zone, and most notably a decrease in Ihh gene expression and proliferation. These defects are reminiscent of the Ihh-/-, PPR-/-(receptor for parathyroid hormone, PTH, and PTH related protein, PTHrP), and PTHrP-/- limb phenotypes. 4. ATF4 transactivates Ihh through directly binding to a cis element of the Ihh promoter. 5. Activation of Ihh signaling restores the size of in Atf4-/- limb in an organ culture system. To test our hypothesis that ATF4 is a regulatory factor for Hedgehog signaling in chondrogenesis, we plan the following specific aims. 1. To determine the molecular mechanisms whereby ATF4 regulates Ihh transcription. 2. To address the role of ATF4 in regulating growth plate chondrocytes proliferation and differentiation in vivo. 3. To demonstrate that Ihh is a direct transcriptional target of ATF4 in vivo. Narrative Indian hedgehog (Ihh) is a well-studied morphogen that regulates the coordination between chondrogenesis and osteogenesis, two processes during skeletal development and bone fracture repair. Surprisingly, investigations on the regulation of Ihh itself are lacking, particularly at the transcriptional level. In this proposal, we intend to investigate this important biological question through systematic molecular and genetic studies.

项目总结/摘要 在软骨内骨形成过程中，成骨和软骨形成是相互联系和高度协调的。 然而，负责协调成骨和软骨形成的调节机制仍然存在， 不清楚遗传小鼠模型已经表明，Hedgehog（Hh）途径，它控制靶基因， 软骨生成如PTHrP和骨生成如BMP 2，对于正常的软骨内骨是必需的 阵然而，尽管其明显的重要性，很少有人知道的监管机制， 负责控制Hedgehog信号这项建议旨在增进对 软骨形成过程中Hedgehog通路的转录控制，特别是Ihh，以及它如何 与骨生成有关由于软骨细胞分化也发生在软骨的早期阶段， 退化以及在骨再生过程中，这项研究直接适用于疾病， 骨关节炎和骨折。我们假设转录因子ATF 4是一个主要的调节因子， 软骨形成过程中的Hedgehog信号传导，也可能在骨形成过程中。我们还 假设ATF 4是Ihh转录直接调节因子。我们的假设基于以下几点 理性 1.我们已经发现，ATF 4对于成骨细胞分化和骨形成是必需的（Yang，et al.，2004年）。 2. Atf 4-缺陷（Atf 4-/-）小鼠是侏儒，表明生长板软骨细胞的缺陷。 3. Atf 4-/-生长板软骨细胞显示出几种异常，包括肥大矿化延迟， 肥大区扩大，最明显的是Ihh基因表达和增殖减少。 这些缺陷使人联想到Ihh-/-、PPR-/-（甲状旁腺激素、PTH和PTH相关的受体）。 蛋白，PTHrP）和PTHrP-/-肢体表型。 4. ATF 4通过直接结合Ihh启动子的顺式元件反式激活Ihh。 5. Ihh信号传导的激活恢复器官培养系统中Atf 4-/-肢的大小。 为了验证我们的假设，即ATF 4是软骨形成中Hedgehog信号传导的调节因子，我们计划在2011年12月至2012年12月期间， 具体目标。 1.确定ATF 4调控Ihh转录的分子机制。 2.探讨ATF 4在体内对生长板软骨细胞增殖和分化的调控作用。 3.证明Ihh是ATF 4在体内的直接转录靶点。叙事 印度刺猬（Ihh）是一个研究充分的形态，调节软骨发生之间的协调 和骨生成，这是骨骼发育和骨折修复过程中的两个过程。令人惊奇的是， 缺乏对Ihh本身调控的研究，特别是在转录水平。在这项提案中， 我们打算通过有系统的分子和遗传学研究来探讨这一重要的生物学问题。

项目成果

Genetic mouse models for bone studies--strengths and limitations.

• DOI: 10.1016/j.bone.2011.08.021
• 发表时间: 2011-12
• 期刊: Bone
• 影响因子: 4.1
• 作者: Elefteriou F;Yang X
• 通讯作者: Yang X

Local low-dose lovastatin delivery improves the bone-healing defect caused by Nf1 loss of function in osteoblasts.

• DOI: 10.1002/jbmr.42
• 发表时间: 2010-07
• 期刊: JOURNAL OF BONE AND MINERAL RESEARCH
• 影响因子: 6.2
• 作者: Wang, Weixi;Nyman, Jeffry S.;Moss, Heather E.;Gutierrez, Gloria;Mundy, Gregory R.;Yang, Xiangli;Elefteriou, Florent
• 通讯作者: Elefteriou, Florent