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骨髓脂肪细胞系祖细胞:一种新兴的破骨细胞微环境细胞群体。

Bone Marrow Adipoq-lineage Progenitors: an Emerging Osteoclast Niche Cell Population.

作者信息

Zhao Baohong, Jiang Jialin

机构信息

Arthritis and Tissue Degeneration Program and David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.

Department of Medicine, Weill Cornell Medical College, New York, NY, USA.

出版信息

Curr Osteoporos Rep. 2025 Sep 12;23(1):37. doi: 10.1007/s11914-025-00933-2.

Abstract

PURPOSE OF REVIEW

The purpose of this review is to summarize and highlight the recent findings of a novel osteoclastic niche centered on the bone marrow Adipoq-lineage progenitors. We will focus on these novel discoveries to help understand the impact of the unique bone marrow Adipoq-lineage cells on osteoclasts, the bone marrow milieu and the skeleton, discuss the similarities and differences between the Adipoq-lineage cells and other bone marrow stromal progenitors, as well as some important questions that draw increasing attention and need to be addressed.

RECENT FINDINGS

Osteoclasts are the exclusive bone-resorbing cells important for bone homeostasis. Osteoclastogenesis is essentially induced by Macrophage colony-stimulating factor (M-CSF) and Receptor activator of nuclear factor kappa-Β ligand (RANKL), meanwhile regulated by other cytokines. Osteoblasts have been long believed to be the major partners of osteoclasts through secretion of M-CSF and RANKL. However, recent groundbreaking findings challenged this traditional model and identified the bone marrow Adipoq-lineage progenitors, not osteoblasts or mature adipocytes, as the main cell type supporting osteoclastogenesis through producing M-CSF, RANKL and other osteoclastogenic cytokines. Recent evidence suggests that the functional impact of the bone marrow Adipoq-lineage progenitors on macrophage lineage development and osteoclastogenesis is very significant. Future studies are expected to elucidate the lineage specification of this cell population and how signaling pathways and environmental cues shape this unique osteoclastic niche in physiological and pathological conditions.

摘要

综述目的

本综述旨在总结并强调以骨髓脂联素谱系祖细胞为中心的新型破骨细胞微环境的最新研究发现。我们将聚焦于这些新发现,以帮助理解独特的骨髓脂联素谱系细胞对破骨细胞、骨髓微环境和骨骼的影响,讨论脂联素谱系细胞与其他骨髓基质祖细胞之间的异同,以及一些日益受到关注且需要解决的重要问题。

最新研究发现

破骨细胞是维持骨稳态的唯一骨吸收细胞。破骨细胞生成主要由巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体(RANKL)诱导,同时受其他细胞因子调控。长期以来,人们一直认为成骨细胞是破骨细胞的主要伙伴,通过分泌M-CSF和RANKL发挥作用。然而,最近的突破性发现挑战了这一传统模型,并确定骨髓脂联素谱系祖细胞而非成骨细胞或成熟脂肪细胞是通过产生M-CSF、RANKL和其他破骨细胞生成细胞因子来支持破骨细胞生成的主要细胞类型。最近的证据表明,骨髓脂联素谱系祖细胞对巨噬细胞谱系发育和破骨细胞生成的功能影响非常显著。未来的研究有望阐明该细胞群体的谱系特异性,以及信号通路和环境线索在生理和病理条件下如何塑造这一独特的破骨细胞微环境。

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