单细胞RNA测序显示,出生后表达Sox9的细胞在小鼠骨骼中占据了大多数骨骼谱系。

IF 5.9 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2025-06-03 DOI:10.1093/jbmr/zjaf043
Neal P Smith, Christopher Janton, Ana Clara Morellato Alcantara, Majd George, Kasidet Mankongtreecheep, Guping Mao, Alexandra-Chloé Villani, Henry M Kronenberg
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引用次数: 0

摘要

在小鼠生长的骨骼中,多种细胞类型有助于成骨细胞谱系,包括生长板软骨细胞、软骨膜细胞和富含cxcl12的网状(CAR)骨髓基质细胞。在这里,我们使用单细胞RNA测序和谱系追踪来显示所有这些成骨细胞前体,甚至是在出生后,都来自表达sox9的祖细胞。我们还描述了位于软骨膜和生长板软骨细胞柱之间的一组独特的软骨细胞,它们有助于成骨细胞谱系。
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Single cell RNA sequencing shows that cells expressing Sox9 postnatally populate most skeletal lineages in mouse bone.

In growing bones of mice, multiple cell types contribute to the osteoblast lineage, including growth plate chondrocytes, perichondrial cells and CXCL12-abundant reticular marrow stromal cells. Here we use single-cell RNA sequencing and lineage tracing to show that all these osteoblast precursors, even postnatally, derives from Sox9-expressing progenitors. We also characterize a distinct group of chondrocytes located between the perichondrium and the columns of growth plate chondrocytes that contribute to the osteoblast lineage.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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