骨细胞
骨髓
骨吸收
骨重建
淋巴细胞生成
细胞生物学
骨免疫学
骨重建期
免疫学
化学
生物
病理
破骨细胞
造血
医学
内分泌学
内科学
干细胞
兰克尔
受体
激活剂(遗传学)
作者
Danka Grčević,Archana Sanjay,Joseph Lorenzo
出处
期刊:Bone
[Elsevier BV]
日期:2021-12-21
卷期号:168: 116296-116296
被引量:27
标识
DOI:10.1016/j.bone.2021.116296
摘要
Bone remodeling occurs through the interactions of three major cell lineages, osteoblasts, which mediate bone formation, osteocytes, which derive from osteoblasts, sense mechanical force and direct bone turnover, and osteoclasts, which mediate bone resorption. However, multiple additional cell types within the bone marrow, including macrophages, T lymphocytes and B lymphocytes influence the process. The bone marrow microenvironment, which is supported, in part, by bone cells, forms a nurturing network for B lymphopoiesis. In turn, developing B lymphocytes influence bone cells. Bone health during homeostasis depends on the normal interactions of bone cells with other lineages in the bone marrow. In disease state these interactions become pathologic and can cause abnormal function of bone cells and inadequate repair of bone after a fracture. This review summarizes what is known about the development of B lymphocytes and the interactions of B lymphocytes with bone cells in both health and disease.
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