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局部因素对破骨细胞分化的调节作用。

Modulation of osteoclast differentiation by local factors.

作者信息

Suda T, Udagawa N, Nakamura I, Miyaura C, Takahashi N

机构信息

Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan.

出版信息

Bone. 1995 Aug;17(2 Suppl):87S-91S. doi: 10.1016/8756-3282(95)00185-g.

Abstract

Bone-resorbing osteoclasts are of hemopoietic cell origin, probably of the CFU-M-derived monocyte-macrophage family. Bone marrow-derived osteoblastic stromal cells play an important role in modulating the differentiation of osteoclast progenitors in two different ways: one is the production of soluble factors, and the other is cell-to-cell recognition between osteoclast progenitors and osteoblastic stromal cells. M-CSF is probably the most important soluble factor, which appears to be necessary for not only proliferation of osteoclast progenitors, but also differentiation into mature osteoclasts and their survival. A number of local factors as well as systemic hormones induce osteoclast differentiation. They are classified into three categories in terms of the signal transduction: vitamin D receptor-mediated signals [1 alpha,25(OH)2D3]; protein kinase A-mediated signals (PTH, PTHrP, PGE2, and IL-1); and gp130-mediated signals (IL-6, IL-11, oncostatin M, and leukemia inhibitory factor). All of these osteoclast-inducing factors appear to act on osteoblastic cells to commonly induce osteoclast differentiation factor (ODF), which recognizes osteoclast progenitors and prepares them to differentiate into mature osteoclasts. This line of approach will undoubtedly produce new ways to treat several metabolic bone diseases caused by abnormal osteoclast recruitment such as osteoporosis, osteopetrosis, Paget's disease, rheumatoid arthritis, and periodontal disease.

摘要

骨吸收破骨细胞起源于造血细胞,可能来自CFU-M衍生的单核细胞-巨噬细胞家族。骨髓来源的成骨基质细胞通过两种不同方式在调节破骨细胞祖细胞分化中发挥重要作用:一种是产生可溶性因子,另一种是破骨细胞祖细胞与成骨基质细胞之间的细胞间识别。M-CSF可能是最重要的可溶性因子,它似乎不仅对破骨细胞祖细胞的增殖是必需的,而且对其分化为成熟破骨细胞及其存活也是必需的。许多局部因子以及全身性激素均可诱导破骨细胞分化。根据信号转导可将它们分为三类:维生素D受体介导的信号[1α,25(OH)2D3];蛋白激酶A介导的信号(甲状旁腺激素、甲状旁腺激素相关蛋白、前列腺素E2和白细胞介素-1);以及gp130介导的信号(白细胞介素-6、白细胞介素-11、制瘤素M和白血病抑制因子)。所有这些诱导破骨细胞的因子似乎都作用于成骨细胞以共同诱导破骨细胞分化因子(ODF),该因子识别破骨细胞祖细胞并使其准备分化为成熟破骨细胞。这种方法无疑将产生新的途径来治疗由破骨细胞募集异常引起的几种代谢性骨疾病,如骨质疏松症、骨质石化症、佩吉特病、类风湿性关节炎和牙周病。

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