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NELL-1 通过整合素β1 促进细胞黏附和分化。

NELL-1 promotes cell adhesion and differentiation via Integrinβ1.

机构信息

Dental and Craniofacial Research Institute and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, Los Angeles, CA 90095, USA.

出版信息

J Cell Biochem. 2012 Dec;113(12):3620-8. doi: 10.1002/jcb.24253.

Abstract

NELL-1 (Nel-like molecule-1) is a secreted osteogenic growth factor first identified in human craniosynostosis (CS) patients. NELL-1 protein has been observed to promote bone and cartilage differentiation and to suppress adipogenesis in both in vitro and in vivo models. Despite these findings, the cell surface receptors of NELL-1 have remained unknown. In this study, we observed for the first time that NELL-1 promotes cell adherence in multiple cell lines, including ST2, C3H10T1/2, M2-10B4, ATDC5, and MC3T3 cells. Additionally, we found that NELL-1 binds to extracellular Integrinβ1 and induces cell focal adhesion. By utilizing siRNA methods, we determined that NELL-1 cell surface binding and enhanced cell attachment were dependent on Integrinβ1 expression. Finally, we observed that pre-coating of culture dishes or PLGA (polylactic-co-glycolic acid) scaffold with NELL-1 resulted in a significant increase in both cell attachment and osteogenic differentiation. Our results identify for the first time a cell surface target of NELL-1, Integrinβ1, and elucidate new functions of NELL-1 in promoting cell adherence and osteogenic differentiation.

摘要

NELL-1(类Nell 分子-1)是一种分泌性成骨生长因子,最初在人类颅缝早闭(CS)患者中被发现。在体外和体内模型中,NELL-1 蛋白被观察到促进骨和软骨分化,并抑制脂肪生成。尽管有这些发现,但 NELL-1 的细胞表面受体仍然未知。在这项研究中,我们首次观察到 NELL-1 促进包括 ST2、C3H10T1/2、M2-10B4、ATDC5 和 MC3T3 在内的多种细胞系的细胞黏附。此外,我们发现 NELL-1 与细胞外整合素β1 结合并诱导细胞焦点黏附。通过使用 siRNA 方法,我们确定了 NELL-1 的细胞表面结合和增强的细胞黏附依赖于整合素β1 的表达。最后,我们观察到用 NELL-1 预先包被培养皿或 PLGA(聚乳酸-共-羟基乙酸)支架可显著增加细胞黏附和成骨分化。我们的研究结果首次确定了 NELL-1 的细胞表面靶标整合素β1,并阐明了 NELL-1 在促进细胞黏附和成骨分化方面的新功能。

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