Laboratory of Lung Inflammation, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Front Immunol. 2020 Feb 28;11:363. doi: 10.3389/fimmu.2020.00363. eCollection 2020.
Proliferation of dendritic cell (DC)-restricted progenitor cells in bone marrow compartment is tightly regulated at steady state and responds to multiple tissue-specific triggers during disturbed homeostasis such as obesity. DCs in the lung stem from a rapidly dividing DC-restricted progenitor cells and are effective at generating adaptive immune responses in allergic airway inflammation. Precisely, how DC-restricted progenitor expansion and differentiation are influenced by airway inflammation to maintain constant supply of myeloid DCs is poorly understood. Here we show that a high fat diet (HFD) induces oxidative stress and accelerates the expansion of DC- restricted progenitor cells in bone marrow and correlates with persistent induction of p38 mitogen activated protein kinase (MAPK), which is blocked with a selective p38α/β MAPK inhibitor. Mice fed a HFD and sensitized to inhaled allergen house dust mite (HDM) led to alterations of DC- restricted progenitor cells that were characterized by increased expansion and seeding of lung DCs in airway inflammation. Mechanistically, we establish that the expansion induced by HFD dysregulates the expression of a disintegrin and metallopeptidase domain 17 (Adam17) and is required for p38 MAPK activation in DC-restricted progenitors. These results demonstrates that obesity produces persistent changes in DC precursors and that elevation of Adam17 expression is tightly coupled to p38 MAPK and is a key driver of proliferation. Altogether, these data provide phenotypic and mechanistic insight into dendritic cell supply chain in obesity-associated airway inflammation.
骨髓腔中树突状细胞(DC)受限前体细胞的增殖在稳态下受到严格调控,并在肥胖等内稳态紊乱时对多种组织特异性触发因素作出反应。肺部的 DC 来源于快速分裂的 DC 受限前体细胞,在变应性气道炎症中有效地产生适应性免疫反应。确切地说,气道炎症如何影响 DC 受限前体细胞的扩增和分化,以维持髓样 DC 的恒定供应,目前还知之甚少。在这里,我们表明高脂肪饮食(HFD)会诱导氧化应激,并加速骨髓中 DC 受限前体细胞的扩增,这与 p38 有丝分裂原激活蛋白激酶(MAPK)的持续诱导相关,而 p38α/β MAPK 抑制剂可阻断其诱导。用 HFD 喂养并对吸入性变应原屋尘螨(HDM)致敏的小鼠导致 DC 受限前体细胞发生改变,其特征是在气道炎症中 DC 的扩增和定植增加。从机制上讲,我们确定 HFD 诱导的扩增会使解整合素和金属蛋白酶域 17(Adam17)的表达失调,这是 DC 受限前体细胞中 p38 MAPK 激活所必需的。这些结果表明,肥胖会导致 DC 前体持续变化,Adam17 表达的升高与 p38 MAPK 密切相关,是增殖的关键驱动因素。总而言之,这些数据为肥胖相关气道炎症中的 DC 供应提供了表型和机制上的深入了解。