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白细胞介素-4和白细胞介素-6基因敲除小鼠的肌腱愈合

Tendon healing in interleukin-4 and interleukin-6 knockout mice.

作者信息

Lin Tony W, Cardenas Luis, Glaser David L, Soslowsky Louis J

机构信息

McKay Orthopaedic Research Laboratory, University of Pennsylvania, 424 Stemmler Hall, 36th and Hamilton Walk, Philadelphia, PA 19104-6081, USA.

出版信息

J Biomech. 2006;39(1):61-9. doi: 10.1016/j.jbiomech.2004.11.009. Epub 2005 Jan 7.

Abstract

Cytokines have been shown to play an important role in tendon and ligament healing by regulating cellular differentiation and activity. The majority of studies that have investigated the role of cytokines in tendon and ligament healing have added them to injured tissue and assessed their effect. Because the efficacy of exogenously applying cytokines is dependent upon many factors such as the correct dosage, timing, and frequency, conflicting results are often reported. To avoid these factors, this study used transgenic mice with knockouts of interleukin-4 (IL4 -/-) and interleukin-6 (IL6 -/-) to investigate their role in tendon healing. Because of the reported roles of both of these cytokines in inflammation and fibroplasia, it was hypothesized that the order of organizational, geometric, and mechanical properties would be (greatest to least) injured IL6 -/-, injured control, and injured IL4 -/- mice. In addition, it was hypothesized that specific cytokines would be upregulated in each knockout group, but not compensate for the lack of IL-4 or IL-6. Mechanical and organizational properties of injured tendons from IL6 -/- mice were inferior to that of control and IL4 -/- mice despite the upregulation of the pro-inflammatory cytokine TNF-alpha. Temporal levels of IL-10 and IL-13 in the IL4 -/- mice resulted in comparable and even superior properties when compared to CTL mice. This study shows that IL-6 could not be compensated for and plays an important role in tendon healing. This study also supports the use of this animal model to further investigate tendon healing.

摘要

细胞因子已被证明通过调节细胞分化和活性在肌腱和韧带愈合中发挥重要作用。大多数研究细胞因子在肌腱和韧带愈合中作用的实验都是将它们添加到受损组织中并评估其效果。由于外源性应用细胞因子的疗效取决于许多因素,如正确的剂量、时间和频率,因此经常报道相互矛盾的结果。为避免这些因素,本研究使用白细胞介素-4基因敲除(IL4 -/-)和白细胞介素-6基因敲除(IL6 -/-)的转基因小鼠来研究它们在肌腱愈合中的作用。鉴于这两种细胞因子在炎症和纤维增生中的作用已有报道,推测组织学、几何学和力学特性的顺序将是(从最大到最小)受伤的IL6 -/-小鼠、受伤的对照小鼠和受伤的IL4 -/-小鼠。此外,推测在每个基因敲除组中特定的细胞因子会上调,但不能弥补IL-4或IL-6的缺失。尽管促炎细胞因子肿瘤坏死因子-α上调,但IL6 -/-小鼠受伤肌腱的力学和组织学特性仍低于对照小鼠和IL4 -/-小鼠。与野生型小鼠相比,IL4 -/-小鼠中IL-10和IL-13的时间水平导致了相当甚至更好的特性。本研究表明,IL-6无法得到代偿,且在肌腱愈合中起重要作用。本研究还支持使用这种动物模型进一步研究肌腱愈合。

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