Stem cells of the suture mesenchyme in craniofacial bone development, repair and regeneration

被引:185
|
作者
Maruyama, Takamitsu [1 ,2 ]
Jeong, Jaeim [1 ]
Sheu, Tzong-Jen [3 ]
Hsu, Wei [1 ,2 ,4 ]
机构
[1] Univ Rochester, Med Ctr, Ctr Oral Biol, Dept Biomed Genet, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Stem Cell & Regenerat Med Inst, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Ctr Musculoskeletal Res, Rochester, NY 14642 USA
[4] Univ Rochester, Med Ctr, Wilmot Canc Inst, Rochester, NY 14642 USA
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
美国国家卫生研究院;
关键词
HAIR FOLLICLE; IN-VITRO; NICHE; WNT; IDENTIFICATION; SPECIFICATION; TISSUES; GROWTH; BMI1;
D O I
10.1038/ncomms10526
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The suture mesenchyme serves as a growth centre for calvarial morphogenesis and has been postulated to act as the niche for skeletal stem cells. Aberrant gene regulation causes suture dysmorphogenesis resulting in craniosynostosis, one of the most common craniofacial deformities. Owing to various limitations, especially the lack of suture stem cell isolation, reconstruction of large craniofacial bone defects remains highly challenging. Here we provide the first evidence for an Axin2-expressing stem cell population with long-term self-renewing, clonal expanding and differentiating abilities during calvarial development and homeostastic maintenance. These cells, which reside in the suture midline, contribute directly to injury repair and skeletal regeneration in a cell autonomous fashion. Our findings demonstrate their true identity as skeletal stem cells with innate capacities to replace the damaged skeleton in cell-based therapy, and permit further elucidation of the stem cell-mediated craniofacial skeletogenesis, leading to revealing the complex nature of congenital disease and regenerative medicine.
引用
收藏
页数:11
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