Smad7在Sox9增强BMP2诱导软骨分化中的作用和机制研究
批准号:
81572142
项目类别:
面上项目
资助金额:
57.0 万元
负责人:
黄伟
依托单位:
学科分类:
骨、关节、软组织损伤与修复
结题年份:
2019
批准年份:
2015
项目状态:
已结题
项目参与者:
梁熙、陈虹、陈诚、廖军义、赵辰、孙泽绪、代光明
中文摘要
BMP2诱导MSC成软骨分化是目前软骨组织工程研究热点,如何增强BMP2促软骨作用,削弱负向因素成为研究重点之一。 我们发现:Sox9可有效增强BMP2诱导软骨化分化的作用,但不能单独诱导软骨化,它是否通过调节BMP2下游发挥促软骨作用?它调节的关键基因又是什么?目前国内外未见报道。Smad7在BMP2诱导软骨化同时被上调,Smad7作为软骨分化的负性因子且近来发现Smad7可能是软骨终末成熟骨化的重要调节因子。那么Sox9是否通过靶向调节Smad7而增强BMP2诱导软骨化的能力?我们发现Sox9可抑制BMP2诱导下的Smad7表达。本项目拟通过研究验证如下假设:1.Sox9通过靶向抑制Smad7促进BMP2的成软骨作用.2.抑制Smad7可阻碍软骨终末成熟骨化。研究结果有助于认识Sox9对Smad7调控关系,Smad7在软骨形成与终末成熟骨化中的作用,为靶向调控软骨组织工程提供新思路。
英文摘要
Cartilaginous pathologies, from degenerative disorders to traumatic injuries, present a very difficult clinical challenge for cartilage lack of regenerative capabilities. While the efficacy of current clinical practices in cartilage repair remains controversial, alternative cartilage tissue engineering is being considered. Bone morphogenetic protein 2 (BMP-2) has been confirmed as one of the most powerful chondrogenic inducer However BMP2 also increase a series of negative factors of chondrogenic differentiation.Our previous studies have shown expression of Sox9 can enhance BMP2-induced chondrogenic marker and inhibit ossification markers while the Sox9 could not induce MSCs chondrogenic differentiation alone.These data suggest Sox9 can regulate BMP2 pathway to enhance chondrgenic differentiation,however the target of Sox9 is unknown. However,Smad7,seem to be potential target for its feature of inhibiting chondrgenic differentiation by blocking Smad1/5/8 and MAPK pathway.Previous studies have shown the potential fact that Smad7 can be related with triggering endochondral ossification and ECM disrupting..Our previous studies have shown expression of Sox9 can enhance BMP-2-induced chondrogenic differentiation and inhibit ossification while the Smad7 being suppressed significantly . The phenomenon indicates Smad7 expression can be downregulated by Sox9.And Smad7 may play dual role in endochondral ossification.But the mechanisms remain unknown.And there is no systemic research about the cellular and molecular mechanisms about that..We attempt to discover that:1.whether Sox9 enhance BMP2 induced chondrogenic differentiation by inhibiting Smad7 or not and the related mechanism .2.whether Smad7 can trigger endochondral ossification in BMP2 induced chondrogenic differentiation.This research aims to find relationship between Sox9 and Smad7 and understand better mechanism of Smad7 .We want to gain optimal cocktail of growth factors and effectors that most effectively to stimulates the generation of cartilage.
软骨缺损是临床上的治疗难点,构建成软骨活性的组织工程软骨具有广阔的运用前景。前期研究发现BMP2介导的间充质干细胞软骨分化是生物工程软骨构建的有效方式,然而BMP2介导的软骨内成骨不利于成软骨分化和软骨表型维持,通过高表达Sox9可有效协同BMP2诱导的成骨,抑制软骨内成骨,我们发现Sox9可能通过抑制Smad7达到了这一效果,然而具体机制尚不清楚,Smad7在BMP2介导的软骨化过程中的作用尚不明确。本课题通过重组腺病毒系统对BMP2介导过程中Smad7的作用及其与Sox9的关系进行了研究,并通过开发生物工程软骨水凝胶为BMP2诱导的软骨形成与稳定提供理想的生物工程材料。本课题指出了生物工程软骨构建与稳定了新干预靶点和信号轴,为生物工程软骨开发提供了理论依据,同时开发了CMC-ACP,GOP生物工程水凝胶,推动软骨组织工程技术的发展和解决临床难题,提供相关实验基础和理论依据.
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A pH-Triggered, Self-Assembled, and Bioprintable Hybrid Hydrogel Scaffold for Mesenchymal Stem Cell Based Bone Tissue Engineering.
一种 pH 触发、自组装、可生物打印的混合水凝胶支架,用于基于间充质干细胞的骨组织工程。
DOI:
10.1021/acsami.8b19094
发表时间:
2019
期刊:
ACS Appl Mater Interfaces
影响因子:
--
作者:
[Zhao Chen, Qazvini Nader Taheri, Sadati Monirosadat, Zeng Zongyue, Huang Shifeng, De La Lastra Ana Losada, Zhang Linghuan, Feng Yixiao, Liu Wei, Huang Bo, Zhang Bo, Dai Zhengyu, Shen Yi, Wang Xi, Luo Wenping, Liu Bo, Lei Yan, Ye Zhenyu, Zhao Ling, Cao Daigui, Yang Lijuan, Che]
通讯作者:
Che
lncRNA H19 mediates BMP9-induced osteogenic differentiation of mesenchymal stem cells (MSCs) through Notch signaling.
lncRNA H19通过Notch信号介导BMP9诱导的间充质干细胞(MSC)成骨分化
DOI:
10.18632/oncotarget.18655
发表时间:
2017-08-08
期刊:
Oncotarget
影响因子:
--
作者:
[Liao J, Yu X, Hu X, Fan J, Wang J, Zhang Z, Zhao C, Zeng Z, Shu Y, Zhang R, Yan S, Li Y, Zhang W, Cui J, Ma C, Li L, Yu Y, Wu T, Wu X, Lei J, Wang J, Yang C, Wu K, Wu Y, Tang J, He BC, Deng ZL, Luu HH, Haydon RC, Reid RR, Lee MJ, Wolf JM, Huang W, He TC]
通讯作者:
He TC
Sox9 augments BMP2-induced chondrogenic differentiation by downregulating Smad7 in mesenchymal stem cells (MSCs).
Sox9 通过下调间充质干细胞 (MSC) 中的 Smad7 增强 BMP2 诱导的软骨形成分化。
DOI:
10.1016/j.gendis.2017.10.004
发表时间:
2017-12
期刊:
Genes & diseases
影响因子:
6.8
作者:
[Zhao C, Jiang W, Zhou N, Liao J, Yang M, Hu N, Liang X, Xu W, Chen H, Liu W, Shi LL, Oliveira L, Wolf JM, Ho S, Athiviraham A, Tsai HM, He TC, Huang W]
通讯作者:
Huang W
DOI:
--
发表时间:
2018
期刊:
中国骨质疏松杂志
影响因子:
--
作者:
[任磊, 代光明, 林枭, 张东力, 田冕, 贺尧, 许文娟, 涂小林, 黄伟]
通讯作者:
黄伟
Enhancement of in vitro proliferation and bioactivity of human anterior cruciate ligament fibroblasts using an in situ tissue isolation method and basic fibroblast growth factor culture conditions A pilot analysis
利用原位组织分离方法和碱性成纤维细胞生长因子培养条件增强人前十字韧带成纤维细胞的体外增殖和生物活性初步分析
DOI:
10.1097/md.0000000000015907
发表时间:
2019
期刊:
Medicine
影响因子:
1.6
作者:
[Liu Ziming, Li Yuwan, Ren Youliang, Jin Ying, Yang Jibin, Wang Shengmin, Zhu Xizhong, Xiong Huazhang, Zou Gang, Liu Yi, Huang Wei]
通讯作者:
Huang Wei
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批准号:U22A20284
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项目类别:联合基金项目
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资助金额:255.00万元
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批准年份:2022
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负责人:黄伟
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依托单位:
Ihh-PTHrP在lncRNA H19调控BMP2诱导的软骨细胞肥大分化中的作用和机制研究
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批准号:81972069
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项目类别:面上项目
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资助金额:55.0万元
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批准年份:2019
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负责人:黄伟
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依托单位:
Sox9对BMP2诱导间充质干细胞成软骨分化的影响及机制研究
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批准号:81371972
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项目类别:面上项目
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资助金额:70.0万元
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批准年份:2013
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负责人:黄伟
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依托单位:
Wnt信号对BMPs诱导干细胞骨向分化的影响及机制研究
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批准号:31070875
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项目类别:面上项目
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资助金额:30.0万元
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批准年份:2010
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负责人:黄伟
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依托单位:
国内基金
海外基金