Torrisi Jeremy S, Hespe Geoffrey E, Cuzzone Daniel A, Savetsky Ira L, Nitti Matthew D, Gardenier Jason C, García Nores Gabriela D, Jowhar Dawit, Kataru Raghu P, Mehrara Babak J
The Department of Surgery, Division of Plastic and Reconstructive Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
Sci Rep. 2016 Jan 22;6:19817. doi: 10.1038/srep19817.
Although recent studies have shown that obesity decreases lymphatic function, the cellular mechanisms regulating this response remain unknown. In the current study, we show that obesity results in perilymphatic accumulation of inflammatory cells and that local inhibition of this response with topical tacrolimus, an inhibitor of T cell differentiation, increases lymphatic vessel density, decreases perilymphatic iNOS expression, increases lymphatic vessel pumping frequency, and restores lymphatic clearance of interstitial fluid to normal levels. Although treatment of obese mice with 1400W, a selective inhibitor of iNOS, also improved lymphatic collecting vessel contractile function, it did not completely reverse lymphatic defects. Mice deficient in CD4(+) cells fed a high fat diet also gained weight relative to controls but were protected from lymphatic dysfunction. Taken together, our findings suggest that obesity-mediated lymphatic dysfunction is regulated by perilymphatic accumulation of inflammatory cells and that T cell inflammatory responses are necessary to initiate this effect.
尽管最近的研究表明肥胖会降低淋巴功能,但调节这种反应的细胞机制仍然未知。在当前的研究中,我们发现肥胖会导致炎症细胞在淋巴管周围积聚,并且用局部他克莫司(一种T细胞分化抑制剂)对这种反应进行局部抑制,可增加淋巴管密度,降低淋巴管周围诱导型一氧化氮合酶(iNOS)的表达,提高淋巴管泵血频率,并将间质液的淋巴清除率恢复到正常水平。虽然用iNOS的选择性抑制剂1400W治疗肥胖小鼠也改善了淋巴管收集血管的收缩功能,但它并没有完全逆转淋巴缺陷。喂食高脂肪饮食的CD4(+)细胞缺陷小鼠相对于对照组也增加了体重,但免受淋巴功能障碍的影响。综上所述,我们的研究结果表明,肥胖介导的淋巴功能障碍是由炎症细胞在淋巴管周围的积聚所调节的,并且T细胞炎症反应是引发这种效应所必需的。