Suppr超能文献

成年哺乳动物滑膜中的关节形成细胞。

Joint morphogenetic cells in the adult mammalian synovium.

机构信息

Arthritis &Regenerative Medicine Laboratory, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK.

出版信息

Nat Commun. 2017 May 16;8:15040. doi: 10.1038/ncomms15040.

Abstract

The stem cells that safeguard synovial joints in adulthood are undefined. Studies on mesenchymal stromal/stem cells (MSCs) have mainly focused on bone marrow. Here we show that lineage tracing of Gdf5-expressing joint interzone cells identifies in adult mouse synovium an MSC population largely negative for the skeletal stem cell markers Nestin-GFP, Leptin receptor and Gremlin1. Following cartilage injury, Gdf5-lineage cells underpin synovial hyperplasia through proliferation, are recruited to a Nestin-GFP perivascular population, and contribute to cartilage repair. The transcriptional co-factor Yap is upregulated after injury, and its conditional ablation in Gdf5-lineage cells prevents synovial lining hyperplasia and decreases contribution of Gdf5-lineage cells to cartilage repair. Cultured Gdf5-lineage cells exhibit progenitor activity for stable chondrocytes and are able to self-organize three-dimensionally to form a synovial lining-like layer. Finally, human synovial MSCs transduced with Bmp7 display morphogenetic properties by patterning a joint-like organ in vivo. Our findings further the understanding of the skeletal stem/progenitor cells in adult life.

摘要

成年后保护滑膜关节的干细胞尚未明确。间充质基质/干细胞(MSCs)的研究主要集中在骨髓。在这里,我们通过 Gdf5 表达的关节间区细胞的谱系追踪表明,在成年小鼠滑膜中存在一种 MSC 群体,其大多数对骨骼干细胞标志物 Nestin-GFP、瘦素受体和 Gremlin1 呈阴性。软骨损伤后,Gdf5 谱系细胞通过增殖支撑滑膜增生,被招募到 Nestin-GFP 血管周细胞群,并有助于软骨修复。转录共激活因子 Yap 在损伤后上调,其在 Gdf5 谱系细胞中的条件性缺失可防止滑膜衬里增生,并减少 Gdf5 谱系细胞对软骨修复的贡献。培养的 Gdf5 谱系细胞表现出稳定的软骨细胞的祖细胞活性,并且能够自我组织成三维结构以形成类似于滑膜衬里的层。最后,转导 Bmp7 的人滑膜间充质干细胞通过在体内形成类似关节的器官显示出形态发生特性。我们的研究结果进一步了解了成年期的骨骼干细胞/祖细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7f8/5493527/9ec442d81303/ncomms15040-f1.jpg

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