Murakami Ichiro, Matsushita Michiko, Iwasaki Takeshi, Kuwamoto Satoshi, Kato Masako, Nagata Keiko, Horie Yasushi, Hayashi Kazuhiko, Imamura Toshihiko, Morimoto Akira, Imashuku Shinsaku, Gogusev Jean, Jaubert Francis, Takata Katsuyoshi, Oka Takashi, Yoshino Tadashi
Division of Molecular Pathology, Faculty of Medicine, Tottori University, 86 Nishi-cho, Yonago, 683-8503, Japan.
Department of Pathobiological Science and Technology, School of Health Science, Faculty of Medicine, Tottori University, Yonago, 683-8503, Japan.
Cell Commun Signal. 2015 Feb 22;13:13. doi: 10.1186/s12964-015-0092-z.
We propose Langerhans cell histiocytosis (LCH) is an inflammatory process that is prolonged by mutations. We hypothesize that Merkel cell polyomavirus (MCPyV) infection triggers an interleukin-1 (IL-1) activation loop that underlies the pathogenesis of LCH. Langerhans cells (LCs) are antigen presenting cells in the skin. When LCs encounter exogenous antigens, they migrate from the epidermis into draining lymphoid tissues to initiate T-cell activity. It has been proposed that LC migration-related factors, including E-cadherin, matrix metalloproteinase, and Notch ligand induce LCH activity. We found that the tyrosine phosphatase SHP-1, which binds IL-1 receptor-associated kinase 1, is expressed at a significantly higher level in LCH affecting multiple organ systems (MS-LCH) than in LCH affecting a single organ system (SS-LCH). IL-1 stimulates T helper 17 cells and their signature cytokine IL-17 had been a matter of controversy. We detected higher levels of IL-17A receptor expression in MS-LCH than in SS-LCH and proposed an IL-17 endocrine model that could settle the controversy. IL-1 is the first cytokine secreted in response to sensitizers and promotes LC migration from sentinel tissues. Myeloid differentiation primary response 88 (MyD88), downstream of the IL-1 receptor, has functions in both RAS signaling and inflammation, leading to human cell transformation. In 2010, an activating mutation in the B-rapidly accelerated fibrosarcoma gene (BRAF) V600E was found in LCH. This BRAF mutation induces phosphorylation of the extracellular signal-regulated kinase (ERK) that may play an important role with MyD88 in LCH pathogenesis. However, phosphorylated ERK (pERK) is rapidly dephosphorylated by dual specificity phosphatase 6 (DUSP6), and limited proliferation is predicted in BRAF mutant cells. MyD88 binds pERK via its D-domain, thereby preventing pERK-DUSP6 interaction and maintaining ERK in an active, phosphorylated state. We detected MCPyV-DNA in the peripheral blood cells of two out of three patients with LCH in high-risk organs but not in those of patients with LCH in non-high-risk organs (0/12; P = .029). MCPyV infection can trigger precursor LCH cells with BRAF mutation to produce IL-1; the IL-1 loop is amplified in all LCH subclasses. Our model indicates both BRAF mutation and IL-1 loop regulation as potential therapeutic targets.
我们提出朗格汉斯细胞组织细胞增多症(LCH)是一种因突变而延长的炎症过程。我们假设默克尔细胞多瘤病毒(MCPyV)感染触发了一个白细胞介素-1(IL-1)激活环,这是LCH发病机制的基础。朗格汉斯细胞(LCs)是皮肤中的抗原呈递细胞。当LCs遇到外源性抗原时,它们从表皮迁移到引流淋巴组织以启动T细胞活性。有人提出,包括E-钙黏蛋白、基质金属蛋白酶和Notch配体在内的与LC迁移相关的因子可诱导LCH活性。我们发现,与IL-1受体相关激酶1结合的酪氨酸磷酸酶SHP-1在影响多器官系统的LCH(MS-LCH)中的表达水平明显高于影响单一器官系统的LCH(SS-LCH)。IL-1刺激辅助性T细胞17,其标志性细胞因子IL-17一直存在争议。我们检测到MS-LCH中IL-17A受体表达水平高于SS-LCH,并提出了一个可以解决这一争议的IL-17内分泌模型。IL-1是对致敏剂作出反应时分泌的第一种细胞因子,并促进LC从哨兵组织迁移。IL-1受体下游的髓样分化初级反应88(MyD88)在RAS信号传导和炎症中均有作用,导致人类细胞转化。2010年,在LCH中发现了B-快速进展性纤维肉瘤基因(BRAF)V600E的激活突变。这种BRAF突变诱导细胞外信号调节激酶(ERK)磷酸化,这可能在LCH发病机制中与MyD88发挥重要作用。然而,磷酸化的ERK(pERK)会被双特异性磷酸酶6(DUSP6)迅速去磷酸化,预计BRAF突变细胞的增殖有限。MyD88通过其D结构域与pERK结合,从而阻止pERK与DUSP6相互作用,并使ERK保持在活性磷酸化状态。我们在三分之二高风险器官LCH患者而非非高风险器官LCH患者(0/12;P = 0.029)的外周血细胞中检测到MCPyV-DNA。MCPyV感染可触发具有BRAF突变的LCH前体细胞产生IL-1;IL-1环在所有LCH亚类中都会放大。我们的模型表明BRAF突变和IL-1环调节均为潜在的治疗靶点。