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骨髓脂肪细胞:血管龛、衰老和疾病中的关键参与者。

Bone marrow adipocytes: key players in vascular niches, aging, and disease.

作者信息

Fan Yonggang, Elkhalek Mai, Zhang Yuheng, Liu Lu, Tian Qi, Chueakula Nareekarn, Ramasamy Saravana K, Dalan Rinkoo, Habib Shukry J, Kusumbe Anjali P

机构信息

Tissue and Tumor Microenvironments Lab, Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.

Multidisciplinary Institute of Ageing (MIA-Portugal), University of Coimbra, Coimbra, Portugal.

出版信息

Front Cell Dev Biol. 2025 Aug 7;13:1633801. doi: 10.3389/fcell.2025.1633801. eCollection 2025.

Abstract

Bone marrow adipocytes (BMAs) are emerging as metabolically active endocrine organs within the bone marrow microenvironment, engaging in extensive crosstalk with vascular niches, osteogenic cells, and hematopoietic compartments. In aging and metabolic disorders, mesenchymal and adipocyte progenitors undergo significant quantitative and qualitative transformations that shift from osteogenesis toward adipogenesis. This enhanced adipogenic profile alters the secretion of key adipokines and cytokines, thereby impairing endothelial function, destabilizing the vascular niche, and reducing hematopoietic stem cell support-culminating in bone fragility and disrupted blood cell production. Central to these alterations are pivotal signaling pathways, which orchestrate the interplay between BMAs and their surrounding cells. Furthermore, factors like oxidative stress, chronic inflammation, and endocrine dysregulation modulate BMA behavior and exacerbate their impact on marrow homeostasis. In this comprehensive review, we integrate recent advances that elucidate the molecular and cellular mechanisms underlying BMA function and their complex interactions with vascular niches. We also discuss therapeutic strategies designed to modulate BMA-mediated pathways and their downstream effects on aging and a range of diseases.

摘要

骨髓脂肪细胞(BMA)正逐渐成为骨髓微环境中具有代谢活性的内分泌器官,与血管龛、成骨细胞和造血区室进行广泛的相互作用。在衰老和代谢紊乱过程中,间充质和脂肪细胞祖细胞会经历显著的数量和质量变化,从成骨向脂肪生成转变。这种增强的脂肪生成特征改变了关键脂肪因子和细胞因子的分泌,从而损害内皮功能,破坏血管龛的稳定性,并减少对造血干细胞的支持,最终导致骨质脆弱和血细胞生成紊乱。这些改变的核心是关键信号通路,它们协调了BMA与其周围细胞之间的相互作用。此外,氧化应激、慢性炎症和内分泌失调等因素调节BMA的行为,并加剧它们对骨髓稳态的影响。在这篇全面的综述中,我们整合了最近的进展,阐明了BMA功能的分子和细胞机制以及它们与血管龛的复杂相互作用。我们还讨论了旨在调节BMA介导的途径及其对衰老和一系列疾病的下游影响的治疗策略。

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