Choi Yura, Park Jeong-Eun, Jeong Jong Seob, Park Jung-Keug, Kim Jongpil, Jeon Songhee
Department of Biomedical Engineering, Dongguk University, Biomedi-Campus, Sangyoung-Bio, Donggul-ro 32, Goyang-si, Gyeonggi-do, 10326, Republic of Korea.
Dongguk University Research Institute of Bio-Medi Integration, Biomedi-Campus, Sangyoung-Bio, Dongguk-ro 32, Goyang-si, Gyeonggi-do, 10326, Republic of Korea.
Appl Biochem Biotechnol. 2016 Oct;180(4):682-694. doi: 10.1007/s12010-016-2124-6. Epub 2016 May 12.
Mesenchymal stem cells (MSCs) have shown considerable promise as an adaptable cell source for use in tissue engineering and other therapeutic applications. The aims of this study were to develop methods to test the hypothesis that human MSCs could be differentiated using sound wave stimulation alone and to find the underlying mechanism. Human bone marrow (hBM)-MSCs were stimulated with sound waves (1 kHz, 81 dB) for 7 days and the expression of neural markers were analyzed. Sound waves induced neural differentiation of hBM-MSC at 1 kHz and 81 dB but not at 1 kHz and 100 dB. To determine the signaling pathways involved in the neural differentiation of hBM-MSCs by sound wave stimulation, we examined the Pyk2 and CREB phosphorylation. Sound wave induced an increase in the phosphorylation of Pyk2 and CREB at 45 min and 90 min, respectively, in hBM-MSCs. To find out the upstream activator of Pyk2, we examined the intracellular calcium source that was released by sound wave stimulation. When we used ryanodine as a ryanodine receptor antagonist, sound wave-induced calcium release was suppressed. Moreover, pre-treatment with a Pyk2 inhibitor, PF431396, prevented the phosphorylation of Pyk2 and suppressed sound wave-induced neural differentiation in hBM-MSCs. These results suggest that specific sound wave stimulation could be used as a neural differentiation inducer of hBM-MSCs.
间充质干细胞(MSCs)作为一种适用于组织工程和其他治疗应用的细胞来源,已显示出巨大的潜力。本研究的目的是开发方法来验证仅使用声波刺激就能使人类间充质干细胞分化的假设,并找出其潜在机制。用声波(1kHz,81dB)刺激人骨髓(hBM)-MSCs 7天,并分析神经标志物的表达。1kHz和81dB的声波可诱导hBM-MSC的神经分化,但1kHz和100dB的声波则不能。为了确定声波刺激hBM-MSCs神经分化所涉及的信号通路,我们检测了Pyk2和CREB的磷酸化情况。在hBM-MSCs中,声波分别在45分钟和90分钟时诱导Pyk2和CREB磷酸化增加。为了找出Pyk2的上游激活剂,我们检测了声波刺激释放的细胞内钙源。当我们使用ryanodine作为ryanodine受体拮抗剂时,声波诱导的钙释放受到抑制。此外,用Pyk2抑制剂PF431396预处理可阻止Pyk2的磷酸化,并抑制hBM-MSCs中声波诱导的神经分化。这些结果表明,特定的声波刺激可作为hBM-MSCs神经分化的诱导剂。