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Gli1 在出生后小鼠的软骨形成过程中标记祖细胞。

Gli1 labels progenitors during chondrogenesis in postnatal mice.

机构信息

State Key Laboratory of Oral Diseases and National Center for Stomatology and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.

Department of Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.

出版信息

EMBO Rep. 2024 Apr;25(4):1773-1791. doi: 10.1038/s44319-024-00093-x. Epub 2024 Feb 26.

Abstract

Skeletal growth promoted by endochondral ossification is tightly coordinated by self-renewal and differentiation of chondrogenic progenitors. Emerging evidence has shown that multiple skeletal stem cells (SSCs) participate in cartilage formation. However, as yet, no study has reported the existence of common long-lasting chondrogenic progenitors in various types of cartilage. Here, we identify Gli1 chondrogenic progenitors (Gli1 CPs), which are distinct from PTHrP or FoxA2 SSCs, are responsible for the lifelong generation of chondrocytes in the growth plate, vertebrae, ribs, and other cartilage. The absence of Gli1 CPs leads to cartilage defects and dwarfishness phenotype in mice. Furthermore, we show that the BMP signal plays an important role in self-renewal and maintenance of Gli1 CPs. Deletion of Bmpr1α triggers Gli1 CPs quiescence exit and causes the exhaustion of Gli1 CPs, consequently disrupting columnar cartilage. Collectively, our data demonstrate that Gli1 CPs are common long-term chondrogenic progenitors in multiple types of cartilage and are essential to maintain cartilage homeostasis.

摘要

软骨内骨化促进的骨骼生长受到软骨祖细胞自我更新和分化的紧密调节。新出现的证据表明,多种骨骼干细胞 (SSCs) 参与软骨形成。然而,迄今为止,尚无研究报道在各种类型的软骨中存在共同的长期软骨祖细胞。在这里,我们鉴定了Gli1 软骨祖细胞 (Gli1 CPs),它们与 PTHrP 或 FoxA2 SSCs 不同,负责生长板、椎体、肋骨和其他软骨中终生的软骨细胞生成。Gli1 CPs 的缺失会导致小鼠出现软骨缺陷和矮小表型。此外,我们表明 BMP 信号在Gli1 CPs 的自我更新和维持中发挥重要作用。Bmpr1α 的缺失会触发 Gli1 CPs 的静止退出并导致 Gli1 CPs 的耗竭,从而破坏柱状软骨。总之,我们的数据表明 Gli1 CPs 是多种类型软骨中的常见长期软骨祖细胞,对于维持软骨稳态至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc4/11014955/72cc7d28a74c/44319_2024_93_Fig1_HTML.jpg

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