Suppr超能文献

锌指和同源盒蛋白 3 对间充质干细胞成骨分化调控的影响。

Impact of zinc fingers and homeoboxes 3 on the regulation of mesenchymal stem cell osteogenic differentiation.

机构信息

Department of Prosthetic Dentistry, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

出版信息

Stem Cells Dev. 2011 Sep;20(9):1539-47. doi: 10.1089/scd.2010.0279. Epub 2011 Feb 24.

Abstract

We propose zinc fingers and homeoboxes 3 (ZHX3) as new osteogenic markers for mesenchymal stem cells (MSC). ZHX3 mRNA expression was upregulated within 1-6 h after incubation of MSCs in the osteogenic induction medium, and reached maximum levels after 24 h of incubation. Two to 4 days later, ZHX3 mRNA levels had decreased sharply. Maximal mRNA levels were 3- to 5-fold higher than those in the undifferentiated state. In contrast, Runt-related transcription factor2 (RUNX2) mRNA expression was downregulated at 2-4 h after incubation, and levels were only enhanced 1.4-fold after 12 and 24 h of incubation. Further, Osterix mRNA levels increased only 1.6-fold after 4 and 24 h of incubation. Thus, ZHX3 expression may be a better marker of MSC osteogenic differentiation than RUNX2 or Osterix expression at the initial stage of differentiation. Knockdown of ZHX3 using 2 distinct small interfering RNA (siRNA) oligonucleotides had little effect on cell morphology or on MSC proliferation, regardless of the differentiation state of the cells. However, ZHX3 siRNAs suppressed Osterix, but not RUNX2 mRNA expression, within 1 h of osteogenic differentiation, and this suppression was sustained for at least 24 h. The 2 ZHX3 siRNAs also suppressed alkaline phosphatase induction and matrix mineralization (assessed using alizarin red staining), and, further, suppressed the calcium content of the cultures at a later stage of differentiation (days 6-21). The effects of ZHX3 siRNAs on the osteogenic differentiation were comparable to those of RUNX2 and Osterix siRNAs. These findings suggest that ZHX3 is involved in the switch from the undifferentiated state of MSC to an osteogenic program, and that ZHX3 may be useful as an early osteogenic differentiation marker.

摘要

我们提出锌指和同源盒蛋白 3(ZHX3)作为间充质干细胞(MSC)成骨的新的标志物。在 MSC 孵育于成骨诱导培养基中 1-6 小时后,ZHX3mRNA 的表达上调,并且在孵育 24 小时后达到最高水平。2 至 4 天后,ZHX3mRNA 水平急剧下降。最大 mRNA 水平比未分化状态高 3-5 倍。相比之下,在孵育 2-4 小时后 runt 相关转录因子 2(RUNX2)mRNA 的表达下调,并且在 12 和 24 小时孵育后仅增强 1.4 倍。此外,在孵育 4 和 24 小时后,osterix mRNA 水平仅增加 1.6 倍。因此,与 RUNX2 或osterix 表达相比,在分化的初始阶段,ZHX3 表达可能是 MSC 成骨分化的更好标志物。使用 2 种不同的小干扰 RNA(siRNA)寡核苷酸敲低 ZHX3 对细胞形态或 MSC 增殖几乎没有影响,而不管细胞的分化状态如何。然而,在成骨分化 1 小时内,ZHX3siRNA 抑制了osterix,但不抑制 RUNX2mRNA 的表达,并且这种抑制持续至少 24 小时。2 种 ZHX3siRNA 还抑制碱性磷酸酶诱导和基质矿化(通过茜素红染色评估),并且进一步在分化后期(第 6-21 天)抑制培养物中的钙含量。ZHX3siRNA 对成骨分化的影响与 RUNX2 和osterixsiRNA 的影响相当。这些发现表明 ZHX3 参与 MSC 从未分化状态向成骨程序的转变,并且 ZHX3 可能作为早期成骨分化标志物有用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验