Bok Seoyeon, Sun Jun, Greenblatt Matthew B
Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York NY 10065, United States.
Skeletal Health and Orthopedic Research Program, Hospital for Special Surgery, New York NY 10065, United States.
J Bone Miner Res. 2024 Sep 26;39(10):1386-1392. doi: 10.1093/jbmr/zjae109.
Only in the past decade have skeletal stem cells (SSCs), a cell type displaying formal evidence of stemness and serving as the ultimate origin of mature skeletal cell types such as osteoblasts, been defined. Here, we discuss a pair of recent reports that identify that SSCs do not represent a single cell type, but rather a family of related cells that each have characteristic anatomic locations and distinct functions tailored to the physiology of those sites. The distinct functional properties of these SSCs in turn provide a basis for the diseases of their respective locations. This concept emerges from one report identifying a distinct vertebral skeletal stem cell driving the high rate of breast cancer metastasis to the spine over other skeletal sites and a report identifying 2 SSCs in the calvaria that interact to mediate both physiologic calvarial mineralization and pathologic calvarial suture fusion in craniosynostosis. Despite displaying functional differences, these SSCs are each united by shared features including a shared series of surface markers and parallel differentiation hierarchies. We propose that this diversity at the level of SSCs in turn translates into a similar diversity at the level of mature skeletal cell types, including osteoblasts, with osteoblasts derived from different SSCs each displaying different functional and transcriptional characteristics reflecting their cell of origin. In this model, osteoblasts would represent not a single cell type, but rather a family of related cells each with distinct functions, paralleling the functional diversity in SSCs.
直到过去十年,骨骼干细胞(SSCs)才得以定义,这是一种显示出干性正式证据并作为成熟骨骼细胞类型(如成骨细胞)最终来源的细胞类型。在此,我们讨论最近的两篇报告,它们指出SSCs并非单一细胞类型,而是一类相关细胞,每个细胞都有特定的解剖位置和适应这些部位生理学的独特功能。这些SSCs的独特功能特性反过来又为其各自部位的疾病提供了基础。这一概念源于一篇报告,该报告鉴定出一种独特的椎骨骨骼干细胞,它驱动乳腺癌向脊柱转移的速率高于其他骨骼部位;另一篇报告则在颅盖骨中鉴定出两种SSCs,它们相互作用以介导生理性颅盖骨矿化和颅缝早闭中的病理性颅盖骨缝融合。尽管这些SSCs表现出功能差异,但它们都具有共同特征,包括一系列共同的表面标志物和平行的分化层次。我们提出,SSCs水平的这种多样性反过来又转化为成熟骨骼细胞类型(包括成骨细胞)水平的类似多样性,源自不同SSCs的成骨细胞各自表现出反映其起源细胞的不同功能和转录特征。在这个模型中,成骨细胞将代表的不是单一细胞类型,而是一类具有不同功能的相关细胞,这与SSCs中的功能多样性相似。