Turner Neill J, Jones Helen S, Davies John E, Canfield Ann E
UK Centre for Tissue Engineering, University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Biochem Biophys Res Commun. 2008 Dec 26;377(4):1147-51. doi: 10.1016/j.bbrc.2008.10.131. Epub 2008 Nov 5.
Human umbilical cord perivascular cells (HUCPVCs) can differentiate along numerous lineages making them a favourable cell source for tissue regeneration. However, how these cells respond to biomechanical forces is unclear. This study aimed to determine whether cyclic stretch could regulate adipogenic differentiation of HUCPVCs, and to elucidate the mechanism of this regulation. In adipogenic culture, HUCPVCs expressed the adipocyte-specific transcription factors PPARgamma and C/EBPalpha and accumulated cytoplasmic lipid droplets. Exposure of these cells to equibiaxial cyclic stretch (10%, 0.5 Hz) in the presence of adipogenic medium, increased Smad2 phosphorylation compared to static samples and inhibited the expression of adipocyte markers; ERK1/2 phosphorylation was not changed. Inhibiting TGFbeta1 signaling decreased Smad2 phosphorylation and prevented the inhibition of adipogenic differentiation by cyclic stretch. These results demonstrate that cyclic equibiaxial stretch regulates HUCPVC differentiation even in the presence of an adipogenic milieu and should be an important consideration in developing future progenitor cell therapies.
人脐带血管周围细胞(HUCPVCs)能够沿着多种谱系分化,使其成为组织再生的理想细胞来源。然而,这些细胞如何响应生物力学力尚不清楚。本研究旨在确定周期性拉伸是否能调节HUCPVCs的成脂分化,并阐明这种调节的机制。在成脂培养中,HUCPVCs表达脂肪细胞特异性转录因子PPARγ和C/EBPα,并积累细胞质脂滴。与静态样本相比,在成脂培养基存在的情况下,将这些细胞暴露于双轴周期性拉伸(10%,0.5Hz)下,可增加Smad2磷酸化,并抑制脂肪细胞标志物的表达;ERK1/2磷酸化未发生变化。抑制TGFβ1信号传导可降低Smad2磷酸化,并阻止周期性拉伸对成脂分化的抑制作用。这些结果表明,即使在存在成脂环境的情况下,双轴周期性拉伸也能调节HUCPVCs的分化,这在未来祖细胞治疗的开发中应是一个重要的考虑因素。