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白血病抑制因子对成骨细胞分化的双相作用。

Biphasic effects of leukemia inhibitory factor on osteoblastic differentiation.

作者信息

Malaval L, Aubin J E

机构信息

INSERM Unité 403, Hôpital Edouard Herriot 5, Place d'Arsonval, 69437 Lyon Cedex 3, France.

出版信息

J Cell Biochem Suppl. 2001;Suppl 36:63-70. doi: 10.1002/jcb.1086.

DOI:10.1002/jcb.1086
PMID:11455571
Abstract

Leukemia inhibitory factor (LIF) is a cytokine produced by multiple cell types including osteoblasts and which is active on bone metabolism. We have previously shown that in a bone nodule forming in vitro model of osteogenesis, the fetal rat calvaria (RC) cell model, LIF inhibits osteoblast differentiation, acting on late osteoprogenitors and/or early osteoblasts. These results are in contrast to in vivo experiments, in which LIF has been found to increase bone formation. To resolve this discrepancy, we have tested the effect of LIF on rat bone marrow (RBM) stromal cell cultures, an in vitro model encompassing earlier osteoprogenitor stages. LIF inhibited cell growth in early, proliferating RBM cultures, but increased the culture saturation density. The effect of LIF on bone nodule formation in this model was cell density dependent and biphasic. Continuous treatment with LIF reduced the number of bone nodules present in confluent, more mature cultures, and the inhibitory effect was strongest when cells were plated at higher cell density than lower. In contrast, during the early stages of RBM culture, nodule numbers were higher in LIF-treated dishes than in controls, and this effect was greater in lower density cultures. Acute LIF treatment restricted to early time points increased the final number of bone nodules formed in mature RBM cell cultures, but not in RC cell cultures. Our results indicate that LIF exerts complex, stage-specific effects on osteoprogenitor recruitment, differentiation, and bone formation, and that the effects are cell nonautonomous, in the rat bone marrow stromal cell model. J. Cell. Biochem. Suppl. 36: 63-70, 2001.

摘要

白血病抑制因子(LIF)是一种由包括成骨细胞在内的多种细胞类型产生的细胞因子,对骨代谢具有活性作用。我们之前已经表明,在体外成骨的骨结节形成模型——胎鼠颅骨(RC)细胞模型中,LIF抑制成骨细胞分化,作用于晚期骨祖细胞和/或早期成骨细胞。这些结果与体内实验相反,在体内实验中发现LIF可增加骨形成。为了解决这一差异,我们测试了LIF对大鼠骨髓(RBM)基质细胞培养物的影响,这是一种涵盖更早骨祖细胞阶段的体外模型。LIF抑制早期增殖的RBM培养物中的细胞生长,但增加了培养物的饱和密度。在该模型中,LIF对骨结节形成的影响取决于细胞密度且具有双相性。用LIF持续处理可减少汇合的、更成熟培养物中存在的骨结节数量,当细胞以较高细胞密度接种时,抑制作用最强,而以较低细胞密度接种时抑制作用较弱。相反,在RBM培养的早期阶段,LIF处理的培养皿中的结节数量高于对照组,且这种效应在低密度培养物中更大。仅在早期时间点进行的急性LIF处理增加了成熟RBM细胞培养物中形成的骨结节的最终数量,但在RC细胞培养物中没有增加。我们的结果表明,在大鼠骨髓基质细胞模型中,LIF对骨祖细胞的募集、分化和骨形成发挥复杂的、阶段特异性的作用,且这些作用是非细胞自主性的。《细胞生物化学杂志》增刊36:63 - 70,2001年。

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