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微小 RNA-142-3p 通过调节 ADAM9 调控 TGF-β3 介导的区域依赖性软骨形成。

MicroRNA-142-3p regulates TGF-β3-mediated region-dependent chondrogenesis by regulating ADAM9.

机构信息

Department of Biological Sciences, College of Natural Sciences, Wonkwang University, Iksan, Chunbuk 570-749, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2011 Nov 4;414(4):653-9. doi: 10.1016/j.bbrc.2011.09.104. Epub 2011 Sep 28.

Abstract

Position-dependent chondrogenesis is regulated by processes that are both common to and differ among all limb types and limb skeletal elements. Despite intrinsic differences between wing and leg bud mesenchyme, the exact regulatory molecules and mechanisms involved in these processes have not been elucidated. Here, we show the limb type-specific role of TGF-β3 during chondrogenic differentiation of chick limb mesenchymal cells. Exposure of wing cells to TGF-β3 stimulated chondrogenic differentiation, whereas in leg bud mesenchymal cells, TGF-β3 induced apoptotic cell death via G2M arrest. Consistent with a limb type-specific effect of TGF-β3 on chondrogenic differentiation, we found different levels of miR-142-3p induction. Inhibition of miR-142-3p via PNA-based antisense oligonucleotides (ASOs) markedly promoted cell migration and precartilage condensation, while exogenous induction of miR-142-3p reduced cell survival and increased cell death. Overexpression of ADAM9 significantly reduced chondrogenic differentiation via downregulation of cell migration and cell survival and upregulation of apoptotic cell death. Limb type-specific expression levels of ADAM9 induced by TGF-β3 were observed. Collectively, this study demonstrates that differential induction of miR-142-3p is involved in the limb type-specific effect of TGF-β3 on wing vs. leg mesenchymal cells through direct modulation of ADAM9 transcription.

摘要

位置依赖的软骨发生受到普遍存在于所有肢体类型和肢体骨骼元素中的过程的调节。尽管翅膀和腿芽间充质之间存在内在差异,但这些过程中涉及的确切调节分子和机制尚未阐明。在这里,我们展示了 TGF-β3 在鸡肢间充质细胞软骨发生分化过程中的肢体类型特异性作用。TGF-β3 暴露于翅膀细胞中会刺激软骨发生分化,而在腿芽间充质细胞中,TGF-β3 通过 G2M 阻滞诱导细胞凋亡。与 TGF-β3 对软骨发生分化的肢体类型特异性效应一致,我们发现 miR-142-3p 的诱导水平不同。通过基于 PNA 的反义寡核苷酸 (ASO) 抑制 miR-142-3p 可显著促进细胞迁移和前软骨凝聚,而外源性诱导 miR-142-3p 则降低细胞存活率并增加细胞死亡。ADAM9 的过表达通过下调细胞迁移和细胞存活以及上调凋亡细胞死亡显著减少软骨发生分化。观察到由 TGF-β3 诱导的 ADAM9 的肢体类型特异性表达水平。总之,这项研究表明,miR-142-3p 的差异诱导参与了 TGF-β3 对翅膀与腿间充质细胞的肢体类型特异性影响,通过直接调节 ADAM9 转录。

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