Schepens Eye Research Institute, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, United States.
Invest Ophthalmol Vis Sci. 2014 Aug 14;55(9):5596-601. doi: 10.1167/iovs.14-14782.
Meibomian gland dysfunction (MGD) is the leading cause of dry eye disease, a prevalent disorder severely affecting patients' quality of life but has no cure. We have discovered that azithromycin, a topical antibiotic used off-label to treat MGD-associated posterior blepharitis, directly acts on the human meibomian gland epithelial cells (HMGECs) to promote their differentiation, and in doing so, reduces cell proliferation. We have also found that insulin-like growth factor-1 (IGF-1), a drug approved by the Food and Drug Administration primarily used to treat dwarfism, stimulates the proliferation and lipid accumulation in these cells. We hypothesize that the combination of azithromycin and IGF-1 will promote cellular differentiation and lipid accumulation, while preserving the normal proliferation of HMGECs.
We cultured immortalized HMGECs with vehicle, 10 nM IGF-1, 10 μg/mL azithromycin, or a combination of IGF-1 and azithromycin for 5 to 13 days. Cells were evaluated for intracellular neutral lipids and lysosome accumulation by different staining methods; lipid composition of cell lysates were analyzed using high-performance thin-layer chromatography; proteins of interest (sterol regulatory element binding protein-1 [SREBP-1], cyclins B1 and D1) were measured by immunoblotting, and cell numbers were counted using a hemocytometer.
Our findings demonstrate that the combination of azithromycin and IGF-1 promotes the differentiation and lipid accumulation of HMGECs, while preserving their normal proliferation rate. This combined treatment also increased the levels of neutral lipids, phospholipids, and SREBP-1, and restored cyclin B1 content to control amounts.
Our results support our hypothesis, and this combination regime may represent a unique and effective treatment of MGD.
睑板腺功能障碍(MGD)是干眼症的主要病因,这是一种普遍存在的疾病,严重影响患者的生活质量,但目前尚无治愈方法。我们发现,阿奇霉素是一种被批准用于治疗 MGD 相关后部睑缘炎的局部抗生素,它可以直接作用于人类睑板腺上皮细胞(HMGEC),促进其分化,同时降低细胞增殖。我们还发现,胰岛素样生长因子-1(IGF-1),一种被美国食品和药物管理局批准的主要用于治疗侏儒症的药物,可刺激这些细胞的增殖和脂质积累。我们假设阿奇霉素和 IGF-1 的联合使用将促进细胞分化和脂质积累,同时保持 HMGEC 的正常增殖。
我们用载体、10 nM IGF-1、10 μg/mL 阿奇霉素或 IGF-1 和阿奇霉素的混合物培养永生化 HMGECs5 至 13 天。通过不同的染色方法评估细胞内中性脂质和溶酶体的积累;使用高效薄层色谱法分析细胞裂解物的脂质组成;通过免疫印迹法测量感兴趣的蛋白质(固醇调节元件结合蛋白-1[SREBP-1]、细胞周期蛋白 B1 和 D1),并用血细胞计数器计数细胞数量。
我们的研究结果表明,阿奇霉素和 IGF-1 的联合使用可促进 HMGECs 的分化和脂质积累,同时保持其正常的增殖率。这种联合治疗还增加了中性脂质、磷脂和 SREBP-1 的水平,并使细胞周期蛋白 B1 含量恢复到对照水平。
我们的研究结果支持我们的假设,这种联合治疗方案可能代表治疗 MGD 的一种独特而有效的方法。