绝经后骨质疏松症中雌激素缺乏介导的骨免疫。

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL Medicinal Research Reviews Pub Date : 2024-09-05 DOI:10.1002/med.22081
Yao Yao, Xiaoyu Cai, Yue Chen, Meng Zhang, Caihong Zheng
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引用次数: 0

摘要

绝经后骨质疏松症(PMO)是一种与衰老相关的常见疾病,雌激素缺乏被认为是导致PMO的主要原因。然而,最近发现骨免疫学与绝经后骨质疏松症密切相关。一方面,雌激素缺乏会直接影响骨细胞(成骨细胞、破骨细胞、骨细胞)的活性。另一方面,雌激素缺乏介导的骨免疫在 PMO 骨质流失中也起着至关重要的作用。在这篇综述中,我们系统地阐述了 PMO 骨质流失机制、雌激素缺乏介导的骨免疫、PMO 患者与绝经后无骨质疏松症人群的差异以及雌激素缺乏介导的免疫细胞(T 细胞、B 细胞、巨噬细胞、中性粒细胞、树突状细胞和肥大细胞)活性的研究进展。本文的全面总结为今后研究 PMO 骨质流失的机制提供了明确的知识背景。
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Estrogen deficiency-mediated osteoimmunity in postmenopausal osteoporosis.

Postmenopausal osteoporosis (PMO) is a common disease associated with aging, and estrogen deficiency is considered to be the main cause of PMO. Recently, however, osteoimmunology has been revealed to be closely related to PMO. On the one hand, estrogen deficiency directly affects the activity of bone cells (osteoblasts, osteoclasts, osteocytes). On the other hand, estrogen deficiency-mediated osteoimmunity also plays a crucial role in bone loss in PMO. In this review, we systematically describe the progress of the mechanisms of bone loss in PMO, estrogen deficiency-mediated osteoimmunity, the differences between PMO patients and postmenopausal populations without osteoporosis, and estrogen deficiency-mediated immune cells (T cells, B cells, macrophages, neutrophils, dendritic cells, and mast cells) activity. The comprehensive summary of this paper provides a clear knowledge context for future research on the mechanism of PMO bone loss.

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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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