Candida albicans secreted protease Sap6 engages epithelial protease-activated receptors PAR2 and NLRP3

白色念珠菌分泌的蛋白酶 Sap6 与上皮蛋白酶激活受体 PAR2 和 NLRP3 结合

基本信息

批准号：
10428637
负责人：
Mira Edgerton
金额：
$ 19.94万
依托单位：
STATE UNIVERSITY OF NEW YORK AT BUFFALO
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-07-01 至 2024-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10428637
关键词：
Apoptosis Aspartic Endopeptidases Bacteria Binding Binding Sites Blocking Antibodies CASP1 gene Calcium Signaling Candida albicans Candidiasis Carbohydrates Caspase Catalytic Domain Cell Surface Receptors Cell Wall Cell surface Cells Cellular Morphology Data Disseminated candidiasis E-Cadherin Electrical Resistance Endocytosis Epithelial Epithelial Cells FOS gene Filament Foundations Fungal Proteins Future Goals Human Hyphae IL17 gene IL8 gene Immunity Immunocompromised Host Inflammasome Inflammation Inflammatory Response Integrin Binding Integrins Interleukin-1 beta Knockout Mice Measurement Measures Mediating Morphology Mucous Membrane Mycoses Neutrophil Infiltration Opportunistic Infections Oral Pathogenicity Pattern recognition receptor Peptide Hydrolases Peptides Permeability Persons Phosphorylation Production Proteinase-Activated Receptors Proteins RGD (sequence)Receptor Signaling Role Signal Pathway Signal Transduction Site Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Surface Symbiosis Testing Therapeutic Virulence Work Yeasts arm cytokine fungus gut microbiota in vivo Model member monocyte mycobiome novel occludin oral bacteria oral cavity epithelium p38 Mitogen Activated Protein Kinase pathogenic fungus receptor receptor internalization release of sequestered calcium ion into cytoplasm treatment strategy

项目摘要

Candida albicans pathogenicity is associated with its morphological transformation from yeast to production of filamentous hyphae. Secretion of hyphal-specific proteins, particularly the aspartyl protease Sap6, is a key marker of its transition from commensalism to virulence. Sap6 contains both a proteinase domain and an RGDRGD integrin-binding motif adjacent to its catalytic domain. We found that rSap6 added to primary oral epithelial cells (OECs) elicited IL1β secretion typical of NLRP3 signaling but also produced IL-8. Sap6 added to OECs induced phosphorylation of p38 and IL-8 production through the protease- activated receptor (PAR2). PAR2 signaling was lost upon heat inactivation of Sap6, while NLRP signaling was reduced upon deletion of Sap6 RGD-binding sites, leading to our hypothesis that both Sap6 proteolytic and RGD-mediated mechanisms are involved in sensing levels of this fungal secreted protein by OECs. We will test this hypothesis by identifying the proteolytic mechanism for Sap6 activated PAR2 MAPKinase signaling in OECs in Aim1, and assessing the contribution of the Sap6 integrin-binding RGD motif in NLRP3 inflammasome activation and apoptosis in Aim 2. This work will establish PAR2 and integrin/NLRP3 as cell surface receptors for C. albicans Sap6 and define their role in modulating host inflammatory responses to fungal proteins in OECs. The long-range goal of this project will be to activate/deactivate PAR2 receptors or NLRP3 signaling as a means of modulating host inflammation as an avenue for treatment of candidiasis.

白色念珠菌的致病性与其从酵母到形态的转变有关。丝状菌丝的产生菌丝特异性蛋白质的分泌，特别是天冬氨酰。蛋白酶 Sap6 是其从共生性向毒力转变的关键标志物。蛋白酶结构域和与其催化结构域相邻的 RGDRGD 整联蛋白结合基序。我们发现添加到原代口腔上皮细胞 (OEC) 中的 rSap6 会引发典型的 IL1β 分泌。 NLRP3 信号传导还产生添加到 OEC 中的 Sap6，诱导 p38 和 p38 的磷酸化。通过蛋白酶激活受体 (PAR2) 产生的 IL-8 因加热而丧失。 Sap6 失活，而 NLRP 信号传导在删除 Sap6 RGD 结合位点后减少，导致我们假设 Sap6 蛋白水解和 RGD 介导的机制都参与我们将通过鉴定 OEC 来检测这种真菌分泌蛋白的水平。 Aim1 中 Sap6 激活 OEC 中 PAR2 MAPKinase 信号传导的蛋白水解机制，以及评估 Sap6 整合素结合 RGD 基序在 NLRP3 炎症小体中的贡献目标 2 中的激活和凋亡。这项工作将建立 PAR2 和整合素/NLRP3 作为细胞表面白色念珠菌 Sap6 受体并定义其在调节宿主炎症反应中的作用该项目的长期目标是激活/停用 PAR2。受体或 NLRP3 信号传导作为调节宿主炎症的一种手段治疗念珠菌病。