Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, P.R. China.
Institute of Sports Biology, Shaanxi Normal University, Xi'an, Shaanxi 710119, P.R. China.
Mol Med Rep. 2017 Dec;16(6):8699-8708. doi: 10.3892/mmr.2017.7720. Epub 2017 Oct 4.
Numerous studies have demonstrated that fluid shear stress (FSS) may promote the proliferation and differentiation of osteoblast cells. However, proliferation and differentiation are mutually exclusive processes and are unlikely to be promoted by FSS simultaneously. Cell proliferation and differentiation induced by FSS has rarely been reported. In order to provide an insight into this process, the present study investigated the effects of FSS on osteoblast‑like MC3T3 cells in the G0/G1 phase, the period during which the fate of a cell is determined. The results of the present study demonstrated that FSS promoted alkaline phosphatase (ALP) activity, and the mRNA expression and protein expression of osteocalcin, collagen type I and runt‑related transcription factor 2 (Runx2), while inhibiting DNA synthesis and arresting the cell cycle at the G0/G1 phase. The increase in Runx2 and ALP activity was accompanied by the activation of calcium/calmodulin‑dependent protein kinase type II (CaMK II) and extracellular signal‑regulated kinases 1/2 (ERK1/2), which was completely abolished by treatment with KN93 and U0126, respectively. In addition, the inhibition of ERK1/2, although not CaMK II, decreased p21Cip/Kip activity, resulting in an increase in cell number and S phase re‑entry. The results of the present study indicated that in the G0/G1 phase, FSS promoted osteoblast differentiation via the CaMK II and ERK1/2 signaling pathways, and blocked the cell cycle at the G0/G1 phase via the ERK1/2 pathway only. The present findings provided an increased understanding of osteoblastic mechanobiology.
大量研究表明,流体切应力(FSS)可能促进成骨细胞的增殖和分化。然而,增殖和分化是相互排斥的过程,不太可能同时被 FSS 促进。FSS 诱导的细胞增殖和分化很少有报道。为了深入了解这一过程,本研究探讨了 FSS 对 G0/G1 期成骨样 MC3T3 细胞的影响,在此期间细胞的命运被决定。本研究结果表明,FSS 促进碱性磷酸酶(ALP)活性,以及骨钙素、I 型胶原和 runt 相关转录因子 2(Runx2)的 mRNA 表达和蛋白表达,同时抑制 DNA 合成并将细胞周期阻滞在 G0/G1 期。Runx2 和 ALP 活性的增加伴随着钙/钙调蛋白依赖性蛋白激酶 II(CaMK II)和细胞外信号调节激酶 1/2(ERK1/2)的激活,分别用 KN93 和 U0126 处理可完全消除该激活。此外,ERK1/2 的抑制作用(而非 CaMK II)降低了 p21Cip/Kip 的活性,导致细胞数量增加和 S 期重新进入。本研究结果表明,在 G0/G1 期,FSS 通过 CaMK II 和 ERK1/2 信号通路促进成骨细胞分化,并通过 ERK1/2 通路仅将细胞周期阻滞在 G0/G1 期。本研究结果提供了对成骨细胞机械生物学的更深入了解。