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Tissue Stretch Decreases Soluble TGF-β1 and Type-1 Procollagen in Mouse Subcutaneous Connective Tissue: Evidence From Ex Vivo and In Vivo Models

机译:组织拉伸降低小鼠皮下结缔组织中的可溶性TGF-β1和1型胶原原:体内和体外模型的证据

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摘要

Transforming growth factor beta 1 (TGF-β1) plays a key role in connective tissue remodeling, scarring, and fibrosis. The effects of mechanical forces on TGF-β1 and collagen deposition are not well understood. We tested the hypothesis that brief (10 min) static tissue stretch attenuates TGF-β1-mediated new collagen deposition in response to injury. We used two different models: (1) an ex vivo model in which excised mouse subcutaneous tissue (N = 44 animals) was kept in organ culture for 4 days and either stretched (20% strain for 10 min 1 day after excision) or not stretched; culture media was assayed by ELISA for TGF-β1; (2) an in vivo model in which mice (N = 22 animals) underwent unilateral subcutaneous microsurgical injury on the back, then were randomized to stretch (20–30% strain for 10 min twice a day for 7 days) or no stretch; subcutaneous tissues of the back were immunohistochemically stained for Type-1 procollagen. In the ex vivo model, TGF-β1 protein was lower in stretched versus non-stretched tissue (repeated measures ANOVA, P < 0.01). In the in vivo model, microinjury resulted in a significant increase in Type-1 procollagen in the absence of stretch (P < 0.001), but not in the presence of stretch (P = 0.21). Thus, brief tissue stretch attenuated the increase in both soluble TGF-β1 (ex vivo) and Type-1 procollagen (in vivo) following tissue injury. These results have potential relevance to the mechanisms of treatments applying brief mechanical stretch to tissues (e.g., physical therapy, respiratory therapy, mechanical ventilation, massage, yoga, acupuncture).
机译:转化生长因子β1(TGF-β1)在结缔组织重塑,瘢痕形成和纤维化中起关键作用。机械力对TGF-β1和胶原蛋白沉积的影响尚不清楚。我们测试了以下假设:短暂的(10分钟)静态组织拉伸会减弱TGF-β1介导的对损伤的新胶原沉积。我们使用了两种不同的模型:(1)一种离体模型,其中将切除的小鼠皮下组织(N = 44只动物)在器官培养物中放置4天,然后拉伸(20%应变,在切除后1天10分钟)伸展通过ELISA测定培养基中的TGF-β1。 (2)一种体内模型,其中小鼠(N = 22只动物)在背部进行了单侧皮下显微外科手术损伤,然后被随机拉伸(20次至30%的应变,每天两次,每次10分钟,共7天)或不拉伸;对背部的皮下组织进行1型胶原蛋白的免疫组织化学染色。在离体模型中,伸展组织中的TGF-β1蛋白低于未伸展组织(重复测量ANOVA,P <0.01)。在体内模型中,在无拉伸的情况下(P <0.001),但在无拉伸的情况下(P = 0.21),微损伤导致Type-1前胶原显着增加。因此,短暂的组织拉伸减弱了组织损伤后可溶性TGF-β1(离体)和1型胶原蛋白(体内)的增加。这些结果与对组织进行短暂机械拉伸的治疗机制(例如物理疗法,呼吸疗法,机械通气,按摩,瑜伽,针灸)具有潜在的相关性。

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