Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Diabetes Metab Res Rev. 2011 Nov;27(8):919-24. doi: 10.1002/dmrr.1272.
Mast cells are essential in allergic responses and beyond. White adipose tissue from obese humans contains large numbers of mast cells. Serum mast cell tryptase levels are also significantly higher in obese subjects than in lean subjects, suggesting a role of these inflammatory cells in obesity and diabetes. Two types of mast cell-deficient mice, along with corresponding wild-type control mice, were fed a Western diet to induce obesity and diabetes. We also used two anti-allergy drugs, cromolyn and ketotifen (Zaditor), to treat wild-type mice during intake of a Western diet or after the onset of obesity and diabetes, to examine the possible prevention or reversal of these conditions. Mast cell deficiency or pharmacological stabilization reduced body weight gain and improved glucose and insulin sensitivities. These common, side effect-free drugs also reduced pre-established obesity and diabetes without noticeable toxicity. Mechanistic studies suggest that mast cells participate in these metabolic disorders by affecting energy expenditure, protease expression, angiogenesis, apoptosis, and preadipocyte differentiation. These observations open a new era of basic research regarding mast cells, and offer hope to patients suffering from these metabolic disorders.
肥大细胞在过敏反应和其他方面是必不可少的。肥胖人群的白色脂肪组织中含有大量的肥大细胞。肥胖受试者的血清肥大细胞胰蛋白酶水平也明显高于瘦受试者,这表明这些炎症细胞在肥胖和糖尿病中起作用。两种类型的肥大细胞缺陷小鼠,以及相应的野生型对照小鼠,被喂食西方饮食以诱导肥胖和糖尿病。我们还使用两种抗过敏药物,色甘酸钠和酮替芬(Zaditor),在摄入西方饮食或肥胖和糖尿病发生后治疗野生型小鼠,以检查这些情况的可能预防或逆转。肥大细胞缺陷或药理稳定减少了体重增加,并改善了葡萄糖和胰岛素敏感性。这些常见的、无副作用的药物还减轻了已建立的肥胖和糖尿病,而没有明显的毒性。机制研究表明,肥大细胞通过影响能量消耗、蛋白酶表达、血管生成、细胞凋亡和前脂肪细胞分化来参与这些代谢紊乱。这些观察结果为肥大细胞的基础研究开辟了一个新时代,并为患有这些代谢紊乱的患者带来了希望。