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骨平衡与破坏

Bone equilibria and disruptions.

作者信息

van Bosse Harold Jacob Pieter

机构信息

St. Louis University School of Medicine, SSM Health/Cardinal Glennon Children's Hospital, St. Louis, MO, USA.

出版信息

J Pediatr Soc North Am. 2024 Apr 6;7:100059. doi: 10.1016/j.jposna.2024.100059. eCollection 2024 May.

Abstract

UNLABELLED

Osteoporosis is considered a disease of adulthood, but there is increasing recognition that poor bone density during childhood can have effects decades later. To understand the pathogenesis of osteoporosis, it is important to understand normal bone maintenance and remodeling, since disruptions of these processes lead to pathologic bone. Bone maintenance is a complex and highly regulated system, consisting of several homeostatic equilibria. This article highlights three homeostatic systems. The first, the interplay between the differentiation of osteoblasts from mesenchymal stem cells and osteoclasts from hematopoietic stem cells, is the most important. Estrogen has a direct effect on the system, and its absence is pivotal. The second is a lesser-known homeostasis that functions between bone and bone marrow adipose tissue, which can insidiously drive osteoporosis. Bone marrow adipose tissue acts as a regulator of bone metabolism, negatively affecting bone formation. The third homeostatic system covered is the microbiota-gut-bone axis, where the make-up of the gut microbiome can influence a balance between osteoblastic and osteoclastic T-cells. Understanding these systems has provided avenues of study for existing and future treatments.

KEY CONCEPTS

(1)The balance between bone formation and bone resorption is driven by factors that initiate the differentiation of mesenchymal stem cells to osteoblasts and hematopoietic stem cells to osteoclasts.(2)Bone marrow adipose tissue is formed by adipocytes that are the result of diversion of mesenchymal stem cells from the osteoblastic differentiation pathway.(3)The health of the gut microbiome has direct effects on the bone homeostatic processes.

摘要

未标注

骨质疏松症被认为是一种成人疾病,但人们越来越认识到儿童时期骨密度不佳可能在数十年后产生影响。为了理解骨质疏松症的发病机制,了解正常的骨骼维持和重塑过程很重要,因为这些过程的破坏会导致病理性骨骼。骨骼维持是一个复杂且高度调节的系统,由几个稳态平衡组成。本文重点介绍三个稳态系统。第一个,间充质干细胞向成骨细胞的分化与造血干细胞向破骨细胞的分化之间的相互作用是最重要的。雌激素对该系统有直接影响,其缺乏是关键因素。第二个是鲜为人知的在骨骼与骨髓脂肪组织之间起作用的稳态,它会潜移默化地导致骨质疏松症。骨髓脂肪组织作为骨代谢的调节因子,对骨形成产生负面影响。涵盖的第三个稳态系统是微生物群 - 肠道 - 骨轴,其中肠道微生物群的组成可影响成骨和破骨T细胞之间的平衡。了解这些系统为现有和未来的治疗提供了研究途径。

关键概念

(1)骨形成与骨吸收之间的平衡由启动间充质干细胞向成骨细胞分化以及造血干细胞向破骨细胞分化的因素驱动。(2)骨髓脂肪组织由脂肪细胞形成,这些脂肪细胞是间充质干细胞从成骨细胞分化途径转移的结果。(3)肠道微生物群的健康对骨骼稳态过程有直接影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/354b/12088274/085f9abe7f7d/gr1.jpg

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