4.8 Article

Hox11 expressing regional skeletal stem cells are progenitors for osteoblasts, chondrocytes and adipocytes throughout life

期刊

NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-11100-4

关键词

-

资金

  1. National Cancer Institute of the National Institutes of Health [P30CA046592]
  2. National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institute of Health (NIH) [R01 AR061402]
  3. National Institute of Dental and Craniofacial Research of the NIH [T32 DE007057]
  4. National Institute of Child Health and Human Development of the NIH [T32 HD007505]
  5. Warner-Lambert Fellowship from University of Michigan Cellular and Molecular Biology training program
  6. University of Michigan Cell and Developmental Biology Bradley M. Patten Fellowship
  7. Michigan Integrative Musculoskeletal Health Core Center [P30 AR069620]

向作者/读者索取更多资源

Multipotent mesenchymal stromal cells (MSCs) are required for skeletal formation, maintenance, and repair throughout life; however, current models posit that postnatally arising long-lived adult MSCs replace transient embryonic progenitor populations. We previously reported exclusive expression and function of the embryonic patterning transcription factor, Hoxa11, in adult skeletal progenitor-enriched MSCs. Here, using a newly generated Hoxa11-CreERT2 lineage-tracing system, we show Hoxa11-lineage marked cells give rise to all skeletal lineages throughout the life of the animal and persist as MSCs. Hoxa11 lineage-positive cells give rise to previously described progenitor-enriched MSC populations marked by LepR-Cre and Osx-CreER, placing them upstream of these populations. Our studies establish that Hox-expressing cells are skeletal stem cells that arise from the earliest stages of skeletal development and self-renew throughout the life of the animal.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据