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首页> 外文期刊>Journal of manipulative and physiological therapeutics: JMPT >Importance of strain direction in regulating human fibroblast proliferation and cytokine secretion: a useful in vitro model for soft tissue injury and manual medicine treatments.
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Importance of strain direction in regulating human fibroblast proliferation and cytokine secretion: a useful in vitro model for soft tissue injury and manual medicine treatments.

机译:应变方向在调节人类成纤维细胞增殖和细胞因子分泌中的重要性:一种有用的体外模型,用于软组织损伤和手动药物治疗。

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OBJECTIVE: Manual medicine treatments (MMTs) rely on biophysical techniques that use manually guided forces in numerous strain directions to treat injuries and somatic dysfunctions. Although clinical outcomes post-MMT are positive, the underlying cellular mechanisms responsible remain elusive. We previously described an in vitro model of strain-induced tissue injury and MMTs. Using this model, the current study sought to determine if strain direction (equibiaxial [EQUI] vs heterobiaxial [HETERO]) differentially regulates human fibroblast function. METHODS: Fibroblasts were strained EQUI at 10% beyond their resting length for 48 hours followed by assessment of cell morphology, proliferation, and cytokine secretion via protein cytokine array and enzyme-linked immunosorbent assay (ELISA). These observations were then compared with those obtained previously for HETERO fibroblasts. RESULTS: No alterations in cell morphology were seen in EQUI fibroblasts despite our report of such changes in HETERO cells. Fibroblasts secretion profiles for 60 cytokines (via cytokine protein array) showed that in EQUI strained cells, fractalkine significantly increased (121%), whereas macrophage-derived chemoattractant/chemokine and pulmonary and activation-regulated chemokine significantly decreased (32% and 10%, respectively) compared with nonstrained cells (P < .05). The EQUI fibroblasts when compared with HETERO fibroblasts exhibited a significant decrease in proliferation (22%), inflammatory interleukin 6 secretion (75%, measured by ELISA), and macrophage-derived chemoattractant/chemokine secretion (177%, measured by ELISA, P < .05). CONCLUSIONS: These divergent observations in HETERO vs EQUI strained fibroblasts may underlie the relative efficacies of MMTs carried out in different tissue strain directions. We are currently modeling MMTs such as myofascial release to further investigate this.
机译:目的:手动药物治疗(MMT)依靠生物物理技术,该技术在多个应变方向上使用手动引导的力来治疗损伤和躯体功能障碍。尽管MMT后的临床结果是积极的,但是负责任的潜在细胞机制仍然难以捉摸。我们先前描述了应变诱发的组织损伤和MMT的体外模型。使用此模型,当前的研究试图确定应变方向(等双轴[EQUI]与异双轴[HETERO])是否会差异调节人类成纤维细胞的功能。方法:将成纤维细胞以超出其静止长度的10%的EQUI应变48小时,然后通过蛋白质细胞因子阵列和酶联免疫吸附测定(ELISA)评估细胞形态,增殖和细胞因子分泌。然后将这些观察结果与先前获得的HETERO成纤维细胞观察结果进行比较。结果:尽管我们报道了HETERO细胞的这种变化,但EQUI成纤维细胞的细胞形态没有变化。 60种细胞因子的成纤维细胞分泌概况(通过细胞因子蛋白阵列)显示,在EQUI应变的细胞中,分数链蛋白显着增加(121%),而巨噬细胞衍生的趋化因子/趋化因子以及经肺和激活调节的趋化因子显着降低(32%和10%,分别与非应变细胞比较(P <.05)。与HETERO成纤维细胞相比,EQUI成纤维细胞的增殖(22%),炎性白介素6分泌(75%,通过ELISA测定)和巨噬细胞来源的趋化因子/趋化因子分泌(177%,通过ELISA测定)显着降低,P < .05)。结论:在HETERO与EQUI应变成纤维细胞中观察到的这些分歧可能是在不同组织应变方向上进行MMT相对效率的基础。我们目前正在对MMT(例如肌筋膜释放)建模,以对此进行进一步调查。

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