Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
LaCell LLC, New Orleans, LA, USA.
Curr Osteoporos Rep. 2018 Jun;16(3):312-319. doi: 10.1007/s11914-018-0442-z.
This review explores how the relationships between bone marrow adipose tissue (BMAT) adipogenesis with advancing age, obesity, and/or bone diseases (osteopenia or osteoporosis) contribute to mechanisms underlying musculoskeletal pathophysiology.
Recent studies have re-defined adipose tissue as a dynamic, vital organ with functions extending beyond its historic identity restricted solely to that of an energy reservoir or sink. "State of the art" methodologies provide novel insights into the developmental origin, physiology, and function of different adipose tissue depots. These include genetic tracking of adipose progenitors, viral vectors application, and sophisticated non-invasive imaging modalities. While constricted within the rigid bone cavity, BMAT vigorously contributes to local and systemic metabolic processes including hematopoiesis, osteogenesis, and energy metabolism and undergoes dynamic changes as a function of age, diet, bone topography, or sex. These insights will impact future research and therapies relating to osteoporosis.
本文探讨了骨髓脂肪组织 (BMAT) 脂肪生成与年龄增长、肥胖和/或骨骼疾病(骨质疏松症或骨质疏松症)之间的关系如何导致肌肉骨骼病理生理学的潜在机制。
最近的研究重新定义了脂肪组织是一种具有多种功能的动态、重要器官,其功能不仅限于作为能量储存或消耗的传统角色。“最先进”的方法为不同脂肪组织储库的发育起源、生理学和功能提供了新的见解。这些方法包括脂肪祖细胞的基因追踪、病毒载体的应用以及复杂的非侵入性成像方式。虽然 BMAT 被限制在刚性的骨腔中,但它强烈地促进了局部和全身代谢过程,包括造血、成骨和能量代谢,并随着年龄、饮食、骨拓扑结构或性别而发生动态变化。这些见解将影响与骨质疏松症相关的未来研究和治疗。