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本文引用的文献

1
Transcription factor Mohawk and the pathogenesis of human anterior cruciate ligament degradation.转录因子莫霍克与人类前交叉韧带退变的发病机制
Arthritis Rheum. 2013 Aug;65(8):2081-9. doi: 10.1002/art.38020.
2
An overview of the management of flexor tendon injuries.屈指肌腱损伤的治疗概述。
Open Orthop J. 2012;6:28-35. doi: 10.2174/1874325001206010028. Epub 2012 Feb 23.
3
Irxl1 mutant mice show reduced tendon differentiation and no patterning defects in musculoskeletal system development.Irxl1突变小鼠在肌肉骨骼系统发育中表现出肌腱分化减少且无模式缺陷。
Genesis. 2011 Jan;49(1):2-9. doi: 10.1002/dvg.20688. Epub 2010 Dec 22.
4
The atypical homeodomain transcription factor Mohawk controls tendon morphogenesis.非典型同源结构域转录因子 Mohawk 控制肌腱形态发生。
Mol Cell Biol. 2010 Oct;30(20):4797-807. doi: 10.1128/MCB.00207-10. Epub 2010 Aug 9.
5
The Mohawk homeobox gene is a critical regulator of tendon differentiation.莫霍克同源盒基因是肌腱分化的关键调节因子。
Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10538-42. doi: 10.1073/pnas.1000525107. Epub 2010 May 24.
6
A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58.系统方法揭示了肌生成基因组网络受转录抑制因子 RP58 的调节。
Dev Cell. 2009 Dec;17(6):836-48. doi: 10.1016/j.devcel.2009.10.011.
7
Fracture-dislocation about the finger joints.手指关节周围的骨折脱位
J Hand Surg Am. 2009 Jul-Aug;34(6):1140-7. doi: 10.1016/j.jhsa.2009.04.023.
8
The basic helix-loop-helix transcription factor scleraxis regulates fibroblast collagen synthesis.碱性螺旋-环-螺旋转录因子硬骨素调节成纤维细胞胶原蛋白的合成。
J Mol Cell Cardiol. 2009 Aug;47(2):188-95. doi: 10.1016/j.yjmcc.2009.03.024. Epub 2009 Apr 10.
9
Tendons and muscles of the mouse forelimb during embryonic development.小鼠胚胎发育期间前肢的肌腱和肌肉
Dev Dyn. 2009 Mar;238(3):693-700. doi: 10.1002/dvdy.21866.
10
The homeobox gene Mohawk represses transcription by recruiting the sin3A/HDAC co-repressor complex.同源异型盒基因莫霍克通过招募sin3A/HDAC共抑制复合物来抑制转录。
Dev Dyn. 2009 Mar;238(3):572-80. doi: 10.1002/dvdy.21873.

莫霍克同源框转录因子调控肌腱和掌侧板的分化。

The Mohawk homeobox transcription factor regulates the differentiation of tendons and volar plates.

作者信息

Onizuka Naoko, Ito Yoshiaki, Inagawa Masayo, Nakahara Hiroyuki, Takada Shuji, Lotz Martin, Toyama Yoshiaki, Asahara Hiroshi

机构信息

Department of Systems BioMedicine, National Center for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, 157-0074, Japan,

出版信息

J Orthop Sci. 2014 Jan;19(1):172-80. doi: 10.1007/s00776-013-0485-z. Epub 2013 Oct 29.

DOI:10.1007/s00776-013-0485-z
PMID:24166359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3943675/
Abstract

BACKGROUND

Mohawk (Mkx) is a homeodomain-containing transcription factor that is expressed in various mesoderm-derived tissues, particularly in developing tendons. In this study, we investigate the exact expression pattern and functions of Mkx in forelimbs.

METHODS

We analyzed the forelimbs of Mkx knockout mice [from embryonic day (E) 18.5 to postnatal day (P) 28 weeks] by using knocked-in Venus signals, Masson trichrome staining, and hematoxylin and eosin (H&E) staining.

RESULTS

We detected Venus signals in forelimb tendons, pulleys, and volar plates (VPs) in P21 mice. In-depth histological analysis showed that compared to the wild-type mice, the Mkx knockout mice showed significant hypoplasia in the flexor digitorum profundus tendons from E18.5. The VPs and pulleys appeared normal until P0; however, by P14, they became increasingly thicker in Mkx-null mice compared to wild-type mice. The fiber alignment was particularly disrupted in VPs of Mkx-null mice.

CONCLUSIONS

These results suggest that Mkx is an important regulator of the differentiation of VPs and pulleys, as well as of tendon differentiation.

摘要

背景

莫霍克(Mkx)是一种含同源结构域的转录因子,在各种中胚层衍生组织中表达,尤其是在发育中的肌腱中。在本研究中,我们调查了Mkx在前肢中的具体表达模式和功能。

方法

我们通过使用敲入的维纳斯信号、马松三色染色和苏木精-伊红(H&E)染色,分析了Mkx基因敲除小鼠的前肢(从胚胎第18.5天到出生后第28周)。

结果

我们在出生后21天小鼠的前肢肌腱、滑车和掌板(VP)中检测到维纳斯信号。深入的组织学分析表明,与野生型小鼠相比,Mkx基因敲除小鼠从胚胎第18.5天起,指深屈肌腱明显发育不全。掌板和滑车在出生后第0天看起来正常;然而,到出生后第14天,与野生型小鼠相比,Mkx基因敲除小鼠的掌板和滑车变得越来越厚。Mkx基因敲除小鼠掌板中的纤维排列尤其紊乱。

结论

这些结果表明,Mkx是掌板和滑车分化以及肌腱分化的重要调节因子。