Regulation of Allergic Asthma by TGF-beta-induced Modulation of mMCP-1 and mMCP-4

通过 TGF-β 诱导的 mMCP-1 和 mMCP-4 调节来调节过敏性哮喘

• 批准号: 8437587
• 负责人: Aparna Bala Sundaram
• 金额: $ 5.94万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-03-01 至 2014-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8437587
• 关键词: Actins; Affect; Agonist; Antibodies; Bathing; Calcium; Cell Degranulation; Chymase; Confocal Microscopy; Data; Development; Down-Regulation; Epithelial Cells; Epithelium; Exposure to; Extrinsic asthma; Future; G-Protein-Coupled Receptors; Generations; Homeostasis; Integrins; Interleukin-13; Knockout Mice; Laboratories; Leukotriene Antagonists; Lung; Mediating; Mus; Muscle; Muscle Contraction; Myosin ATPase; Myosin Light Chain Kinase; Pathogenesis; Pathway interactions; Peptide Hydrolases; Play; Process; Regulation; Research Proposals; Role; Slice; Smooth Muscle; Smooth Muscle Myocytes; System; Transforming Growth Factor beta; Transforming Growth Factors; Up-Regulation; Work; airway epithelium; airway hyperresponsiveness; anti-IgE; mast cell; methacholine; myosin phosphatase; novel; research study; respiratory smooth muscle; response; therapeutic target; voltage

DESCRIPTION (provided by applicant): Transforming growth factor-¿ (TGF-¿) has been strongly implicated in the development of allergic asthma. Mast cell degranulation also plays a key role in exacerbating allergic asthma, and is the therapeutic target of both leukotriene antagonists and anti-IgE antibodies. Recent data from our laboratory has suggested that mice lacking the ¿v¿6 integrin, which modulates TGF-¿ activity, are protected from airway hyperreactivity. Furthermore, this effect is mediated by differential mast cell protease expression induced by TGF-¿, namely via the upregulation of mMCP-1 and the downregulation of mMCP-4. These proteases have been shown to influence airway hyperreactivity, with mMCP-1 augmenting smooth muscle contraction in response to methacholine and mMCP-4 inhibiting IL-13 induced contraction. In this proposal we will systematically investigate the mechanism by which mMCP-1 and mMCP-4 affect contractile response using parallel experimental systems (tracheal ring contraction in muscle bath and airway narrowing in lung slices). We will use constructs of mMCP-1-, and mMCP-4- knockout mice to assess what contribution the interaction of TGF-¿ with mast cells makes to the contractile response. We propose to determine whether mMCP-1 and mMCP-4 act directly on smooth muscle or indirectly via adjacent epithelial cells. Since force generation in smooth muscle depends on Ca2+-dependent actin-myosin cross-bridging, we will also investigate how mMCP-1 and mMCP-4 modulate Ca2+ homeostasis. The proposed studies will elucidate the mechanism by which TGF-¿-modulated expression of mast cell proteases mMCP-1 and mMCP-4 affect airway hyperreactivity. As this pathway plays an important role in the pathogenesis of allergic asthma, a more thorough understanding will provide potential targets for future therapy.

描述（由申请人提供）：转化生长因子-<$（TGF-<$）与过敏性哮喘的发生密切相关。肥大细胞脱颗粒也在加重过敏性哮喘中起关键作用，并且是白三烯拮抗剂和抗IgE抗体的治疗靶点。我们实验室的最新数据表明，缺乏调节TGF-β活性的β v β 6整合素的小鼠受到保护，免受气道高反应性的影响。此外，这种作用是由差异肥大细胞蛋白酶表达介导的 通过TGF-β诱导，即通过mMCP-1的上调和mMCP-4的下调。这些蛋白酶已显示影响气道高反应性，其中mMCP-1响应乙酰甲胆碱而增强平滑肌收缩，而mMCP-4抑制IL-13诱导的收缩。在这个建议中，我们将系统地研究mMCP-1和mMCP-4影响收缩反应的机制，使用平行的实验系统（气管环收缩在肌肉浴和气道狭窄的肺切片）。我们将使用mMCP-1和mMCP-4基因敲除小鼠的构建体来评估TGF-β与肥大细胞的相互作用对收缩反应的贡献。我们建议确定mMCP-1和mMCP-4是否直接作用于平滑肌或间接通过相邻的上皮细胞。由于平滑肌中的力产生依赖于Ca 2+依赖性肌动蛋白-肌球蛋白交联，我们还将研究mMCP-1和mMCP-4如何调节Ca 2+稳态。这些研究将阐明TGF-β调节肥大细胞蛋白酶mMCP-1和mMCP-4表达影响气道高反应性的机制。由于这一通路在过敏性哮喘的发病机制中起着重要作用，因此对其深入的了解将为未来的治疗提供潜在的靶点。