Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan.
Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan; Research Center of Health, Physical Fitness and Sports, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan.
Neurochem Int. 2020 Jun;136:104733. doi: 10.1016/j.neuint.2020.104733. Epub 2020 Mar 25.
Glial cells can mediate hypothalamic inflammatory processes induced in response to a high-fat diet (HFD). We used magnetic-activated cell sorting (MACS) to isolate microglia and astrocytes from hypothalamus of mice fed HFD and examined changes in expression of inflammation-related cytokines and markers related to glial cell activation status. Hypothalamus from male C57BL6 mice fed a chow diet (chow) or HFD for 1, 3, or 28 days were collected and microglia and astrocytes were isolated by MACS. After confirming cell viability by fluorescence activated cell sorting, mRNA expression levels of inflammation-related cytokines and markers of glial cell activation status were examined by qRT-PCR, which revealed that both glial cell types isolated by MACS retained specificity. On day 3 of HFD, both CD86 and TNFα mRNA expression was significantly increased in microglia relative to the chow group. In astrocytes, TNFα mRNA expression levels were similar between the chow and HFD groups on day 3, but anti-inflammatory cytokine IL-10 levels were significantly increased. On day 7 of HFD, TNFα expression in microglia decreased to levels comparable to the chow group while that in astrocytes remained unchanged. On day 28 of HFD, TNFα levels were significantly increased in both microglia and astrocytes, which had increased mRNA expression of CD86 and MAO-B, respectively. For both glial cell types, results for TNFα expression assessed by RT-PCR and immunohistochemical analysis were similar. These results indicate that the role of microglia and astrocytes in hypothalamic inflammation under HFD conditions changed with time and these changes were accompanied by changes in the activation status of glial cells. Our data suggest that early after initiating HFD, hypothalamic astrocytes suppress diet-induced inflammation at least in part by secreting IL-10, whereas continued HFD feeding impairs this suppressive function such that both microglia and astrocytes promote hypothalamic inflammation.
神经胶质细胞可以介导高脂肪饮食(HFD)引起的下丘脑炎症过程。我们使用磁激活细胞分选(MACS)从小鼠的下丘脑分离小胶质细胞和星形胶质细胞,研究炎症相关细胞因子和与胶质细胞激活状态相关标志物的表达变化。收集雄性 C57BL6 小鼠喂食标准饮食(对照)或 HFD 1、3 或 28 天的下丘脑,通过 MACS 分离小胶质细胞和星形胶质细胞。通过荧光激活细胞分选确认细胞活力后,通过 qRT-PCR 检测炎症相关细胞因子和胶质细胞激活状态标志物的 mRNA 表达水平,结果表明通过 MACS 分离的两种神经胶质细胞类型均保留了特异性。在 HFD 的第 3 天,与对照相比,小胶质细胞中 CD86 和 TNFα mRNA 的表达显著增加。在星形胶质细胞中,第 3 天对照和 HFD 组之间 TNFα mRNA 表达水平相似,但抗炎细胞因子 IL-10 水平显著增加。在 HFD 的第 7 天,小胶质细胞中 TNFα 的表达水平降低到与对照相似的水平,而星形胶质细胞中的表达水平保持不变。在 HFD 的第 28 天,小胶质细胞和星形胶质细胞中 TNFα 水平均显著升高,分别导致 CD86 和 MAO-B 的 mRNA 表达增加。对于两种神经胶质细胞类型,通过 RT-PCR 和免疫组织化学分析评估的 TNFα 表达结果相似。这些结果表明,在 HFD 条件下,小胶质细胞和星形胶质细胞在下丘脑炎症中的作用随时间而变化,这些变化伴随着神经胶质细胞激活状态的变化。我们的数据表明,在开始 HFD 后不久,下丘脑星形胶质细胞通过分泌 IL-10 至少部分抑制饮食引起的炎症,而持续的 HFD 喂养会损害这种抑制功能,导致小胶质细胞和星形胶质细胞均促进下丘脑炎症。