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压应力调控的成骨细胞的大小依赖性反应。

Magnitude-dependent response of osteoblasts regulated by compressive stress.

机构信息

Department of Stomatology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.

School of Dentistry, University of Detroit Mercy, Detroit, Michigan, USA.

出版信息

Sci Rep. 2017 Mar 20;7:44925. doi: 10.1038/srep44925.

Abstract

The present study aimed to investigate the role of magnitude in adaptive response of osteoblasts exposed to compressive stress. Murine primary osteoblasts and MC3T3-E1 cells were exposed to compressive stress (0, 1, 2, 3, 4, and 5 g/cm) in 3D culture. Cell viability was evaluated, and expression levels of Runx2, Alp, Ocn, Rankl, and Opg were examined. ALP activity in osteoblasts and TRAP activity in RAW264.7 cells co-cultured with MC3T3-E1 cells were assayed. Results showed that compressive stress within 5.0 g/cm did not influence cell viability. Both osteoblastic and osteoblast-regulated osteoclastic differentiation were enhanced at 2 g/cm. An increase in stress above 2 g/cm did not enhance osteoblastic differentiation further but significantly inhibited osteoblast-regualted osteoclastic differentiation. This study suggested that compressive stress regulates osteoblastic and osteoclastic differentiation through osteoblasts in a magnitude-dependent manner.

摘要

本研究旨在探讨在受压应力下成骨细胞适应反应中幅度的作用。将鼠原代成骨细胞和 MC3T3-E1 细胞暴露于 3D 培养中的压缩应力(0、1、2、3、4 和 5 g/cm)下。评估细胞活力,并检查 Runx2、Alp、Ocn、Rankl 和 Opg 的表达水平。测定成骨细胞中的碱性磷酸酶(ALP)活性和与 MC3T3-E1 细胞共培养的 RAW264.7 细胞中的破骨细胞 TRAP 活性。结果表明,5.0 g/cm 以内的压缩应力不会影响细胞活力。在 2 g/cm 时,成骨细胞和成骨细胞调节的破骨细胞分化均增强。超过 2 g/cm 的应力增加不会进一步增强成骨细胞分化,但会显著抑制成骨细胞调节的破骨细胞分化。本研究表明,压缩应力通过成骨细胞以依赖幅度的方式调节成骨细胞和破骨细胞分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70ee/5357902/8b1346738bdc/srep44925-f1.jpg

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