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白细胞介素-6 调节淋巴水肿中的脂肪沉积和稳态。

IL-6 regulates adipose deposition and homeostasis in lymphedema.

机构信息

The Department of Surgery, Division of Plastic and Reconstructive Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York;

The Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York;

出版信息

Am J Physiol Heart Circ Physiol. 2014 May 15;306(10):H1426-34. doi: 10.1152/ajpheart.01019.2013. Epub 2014 Mar 14.

Abstract

Lymphedema (LE) is a morbid disease characterized by chronic limb swelling and adipose deposition. Although it is clear that lymphatic injury is necessary for this pathology, the mechanisms that underlie lymphedema remain unknown. IL-6 is a known regulator of adipose homeostasis in obesity and has been shown to be increased in primary and secondary models of lymphedema. Therefore, the purpose of this study was to determine the role of IL-6 in adipose deposition in lymphedema. The expression of IL-6 was analyzed in clinical tissue specimens and serum from patients with or without LE, as well as in two mouse models of lymphatic injury. In addition, we analyzed IL-6 expression/adipose deposition in mice deficient in CD4(+) cells (CD4KO) or IL-6 expression (IL-6KO) or mice treated with a small molecule inhibitor of IL-6 or CD4 depleting antibodies to determine how IL-6 expression is regulated and the effect of changes in IL-6 expression on adipose deposition after lymphatic injury. Patients with LE and mice treated with lymphatic excision of the tail had significantly elevated tissue and serum expression of IL-6 and its downstream mediator. The expression of IL-6 was associated with adipose deposition and CD4(+) inflammation and was markedly decreased in CD4KO mice. Loss of IL-6 function resulted in significantly increased adipose deposition after tail lymphatic injury. Our findings suggest that IL-6 is increased as a result of adipose deposition and CD4(+) cell inflammation in lymphedema. In addition, our study suggests that IL-6 expression in lymphedema acts to limit adipose accumulation.

摘要

淋巴水肿(LE)是一种以慢性肢体肿胀和脂肪沉积为特征的病态疾病。尽管淋巴损伤是这种病理学的必要条件,但导致淋巴水肿的机制尚不清楚。IL-6 是肥胖症中脂肪稳态的已知调节剂,并且已在原发性和继发性淋巴水肿模型中显示出增加。因此,本研究的目的是确定 IL-6 在淋巴水肿中的脂肪沉积中的作用。分析了有或没有 LE 的患者的临床组织标本和血清中的 IL-6 表达,以及两种淋巴损伤的小鼠模型中的 IL-6 表达。此外,我们分析了缺乏 CD4(+)细胞(CD4KO)或 IL-6 表达(IL-6KO)的小鼠或用 IL-6 或 CD4 耗竭抗体的小分子抑制剂治疗的小鼠中的 IL-6 表达/脂肪沉积,以确定 IL-6 表达如何被调节以及 IL-6 表达的变化对淋巴损伤后脂肪沉积的影响。有 LE 的患者和接受尾部淋巴管切除的小鼠的组织和血清中 IL-6 及其下游介质的表达明显升高。IL-6 的表达与脂肪沉积和 CD4(+)炎症有关,在 CD4KO 小鼠中明显降低。IL-6 功能丧失导致尾部淋巴损伤后脂肪沉积明显增加。我们的研究结果表明,IL-6 是由于淋巴水肿中的脂肪沉积和 CD4(+)细胞炎症而增加的。此外,我们的研究表明,淋巴水肿中的 IL-6 表达可限制脂肪堆积。

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