Chen Renqiong, Ji Guangquan, Wang Ling, Ren Hong, Xi Liyan
Department of Dermatology, Lianyungang First People's Hospital, Lianyungang, 222002, China; Department of Dermatology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, 510120, China.
Department of Dermatology, Lianyungang First People's Hospital, Lianyungang, 222002, China.
Microb Pathog. 2016 Apr;93:95-9. doi: 10.1016/j.micpath.2016.01.026. Epub 2016 Jan 30.
Previous study have shown that Penicillium marneffei (P. marneffei)-induced TNF-α production via an extracellular signal-regulated kinase (ERK) mitogen-activated protein kinase-dependent mechanism is an important host defence mechanism against P. marneffei in human macrophages. Therefore, we explore signaling pathway that regulates TNF-α secretion and activation of ERK1/2 by intracellular signaling mechanisms during P. marneffei infection. We found that ERK1/2 activation was dependent on the calcium/calmodulin/calmodulin kinase Ⅱ pathway in P. marneffei-infected human macrophages. In contrast, P. marneffei-induced p38 MAPK activation was negatively regulated by calcium/calmodulin/calmodulin kinase Ⅱ signaling pathway. Furthermore, TNF-α production in P. marneffei-infected human macrophages was also dependent on Ca(2+)/calmodulin/calmodulin kinase Ⅱ pathway. These data suggest that Ca(2+)/calmodulin/calmodulin kinase Ⅱ pathway plays vital regulatory roles in macrophage activation and subsequent cytokine production during P. marneffei infection.
先前的研究表明,马尔尼菲青霉通过细胞外信号调节激酶(ERK)丝裂原活化蛋白激酶依赖性机制诱导肿瘤坏死因子-α(TNF-α)产生,这是人类巨噬细胞抵御马尔尼菲青霉的重要宿主防御机制。因此,我们探索了马尔尼菲青霉感染期间通过细胞内信号机制调节TNF-α分泌和ERK1/2激活的信号通路。我们发现,在马尔尼菲青霉感染的人类巨噬细胞中,ERK1/2的激活依赖于钙/钙调蛋白/钙调蛋白激酶Ⅱ途径。相反,马尔尼菲青霉诱导的p38丝裂原活化蛋白激酶激活受到钙/钙调蛋白/钙调蛋白激酶Ⅱ信号通路的负调控。此外,马尔尼菲青霉感染的人类巨噬细胞中TNF-α的产生也依赖于Ca(2+)/钙调蛋白/钙调蛋白激酶Ⅱ途径。这些数据表明,Ca(2+)/钙调蛋白/钙调蛋白激酶Ⅱ途径在马尔尼菲青霉感染期间巨噬细胞活化及随后的细胞因子产生中发挥着至关重要的调节作用。