4.8 Article

Noncoding dsRNA induces retinoic acid synthesis to stimulate hair follicle regeneration via TLR3

期刊

NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-10811-y

关键词

-

资金

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases, part of the National Institutes of Health [R01AR064297, AR068280]
  2. Department of Defense, Armed Forces Institute of Regenerative Medicine, Extremities Regeneration [AFIRM2-ER11]
  3. Northrop Grumman Electronic Systems
  4. Thomas Provost, MD Young Faculty Development Fund of Johns Hopkins Dermatology
  5. Maryland Stem Cell Research Grant [2017-MSCRFF-3905]
  6. Eunice Kennedy Shriver National Institute of Child Health and Human Development, part of the National Institutes of Health [R01HD077260]
  7. University of Maryland School of Pharmacy Mass Spectrometry Center [SOP1841-IQB2014]
  8. CDMRMP [W81XWH-16-C-0167]

向作者/读者索取更多资源

How developmental programs reactivate in regeneration is a fundamental question in biology. We addressed this question through the study of Wound Induced Hair follicle Neogenesis (WIHN), an adult organogenesis model where stem cells regenerate de novo hair follicles following deep wounding. The exact mechanism is uncertain. Here we show that self-noncoding dsRNA activates the anti-viral receptor toll like receptor 3 (TLR3) to induce intrinsic retinoic acid (RA) synthesis in a pattern that predicts new hair follicle formation after wounding in mice. Additionally, in humans, rejuvenation lasers induce gene expression signatures for dsRNA and RA, with measurable increases in intrinsic RA synthesis. These results demonstrate a potent stimulus for RA synthesis by non-coding dsRNA, relevant to their broad functions in development and immunity.

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