Key Lab of Chemical Biology, Ministry of Education (MOE), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China.
Suzhou Research Institute, Shandong University, Suzhou, China.
Front Endocrinol (Lausanne). 2022 Sep 5;13:965290. doi: 10.3389/fendo.2022.965290. eCollection 2022.
Bone development have been shown to play an important role in regulating hematopoiesis as one major component of bone marrow microenvironment. Recent studies support the notion that there is an intricate relationship between hematopoiesis and bone homeostasis, however, little is known about the alterations in the hematopoietic lineages in pathologic conditions. Using various osteoporotic mouse models, we show here that bone microarchitecture abnormalities alter parameters of peripheral blood cells. The level of white blood cells is dynamics and negatively correlated with bone mineral density during the progression of osteoporosis. Furthermore, our clinical data confirm that osteoporosis is associated with abnormal circulating blood cell counts. These results demonstrated a causal link that osteoporosis is accompanied by the altered circulating blood cells, supporting the idea of a close interplay between hematopoiesis and bone homeostasis. Our study would propose that routine complete blood count might be applied as a potential diagnostic and putative marker for osteoporosis.
骨骼发育在调节造血中起着重要作用,是骨髓微环境的主要组成部分之一。最近的研究支持这样一种观点,即造血和骨骼稳态之间存在着复杂的关系,然而,对于病理条件下造血谱系的改变知之甚少。我们使用各种骨质疏松症小鼠模型,在此表明骨微结构异常改变外周血细胞的参数。在骨质疏松症进展过程中,白细胞的水平是动态的,与骨矿物质密度呈负相关。此外,我们的临床数据证实,骨质疏松症与循环血细胞计数异常有关。这些结果表明了一种因果关系,即骨质疏松症伴随着循环血细胞的改变,支持了造血和骨骼稳态之间密切相互作用的观点。我们的研究表明,常规全血细胞计数可能被用作骨质疏松症的一种潜在诊断和标记物。