Defining the role of S1p and myeloid cells during enterotoxigenic B. fragilis infection
Defining the role of S1p and myeloid cells during enterotoxigenic B. fragilis infection
批准号:
10369893
负责人:
Zhong-Bin Deng
金额:
$23.41万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-22 至 2023-08-31
关键词:
Acetyl Coenzyme AAcute DiarrheaAnaerobic BacteriaApcMin/+ miceBacteroides fragilisCell ProliferationCell physiologyCellsCellular Metabolic ProcessCeramidaseCeramidesColitisColonColorectal CancerDataDevelopmentDietDinoprostoneDiseaseEnvironmentEnzymesEpithelialEpithelial CellsFatty AcidsGeneral PopulationGenesHistone AcetylationHumanITGAM geneImmuneInfectionInflammationInflammatoryInflammatory Bowel DiseasesInflammatory ResponseInnate Immune ResponseInterleukin-17IntestinesLeadLinkLipidsLiverLymphocyte FunctionMetabolicMetabolismModelingMusMyelogenousMyeloid CellsMyeloid-derived suppressor cellsNuclearPPAR gammaPTGS2 genePathogenesisPathway interactionsPhosphorylationProductionPropertyProteinsReactionRegulationRoleShapesSignal TransductionSphingolipidsSphingosineSteroidsTestingTherapeuticToxinTranslatingblood glucose regulationcell motilitycolon tumorigenesisdietary sphingolipidsextracellulargene inductiongranulocytegut bacteriagut dysbiosishistone modificationinflammatory disease of the intestineintestinal epitheliumlipid metabolismmicrobialmigrationmonocytenew therapeutic targetpolarized cellpromoterrecruitresponsesphingosine 1-phosphatesphingosine kinasetumorigenesis
中文摘要
产肠毒素脆弱类杆菌(ETBF)与急性腹泻有关,
炎症性肠病和结肠直肠癌(CRC)。ETBF肿瘤发生需要
其毒素BFT和炎症反应的协调作用,以协调招募
但是ETBF如何募集结肠髓样细胞仍然知之甚少。S1p行为
作为生物活性的鞘脂信使,影响骨髓细胞的迁移和调节
结肠炎然而,ETBF是否整合了鞘脂代谢产物来确定
结肠髓样细胞的代谢需要探索。最近的证据表明,
髓样细胞代谢的重塑是诱导先天免疫应答的关键。
我们发现ETBF感染改变了鞘氨醇激酶的活性,这与代谢有关。
骨髓细胞中的重塑、组蛋白乙酰化和PGE2产生。两个综合具体
目的1将确定ETBF感染如何调节炎症
骨髓细胞在结肠中积聚。目标2将确定乙酰辅酶A的ETBF是否改变
通过PPARγ活化促进髓样细胞的代谢重塑。更深刻的认识
鞘脂及其酶在控制肠道免疫中的适当作用
性质和促进结肠炎的发病和进展将产生新的
“以鞘脂为中心”的治疗策略,控制
ETBF诱导的肠道炎症的发作和持续。
英文摘要
Enterotoxigenic Bacteroides fragilis (ETBF) has been associated with acute diarrheal,
inflammatory bowel disease, and colorectal cancer (CRC). ETBF oncogenesis requires the
coordinated action of its toxin, BFT, and an inflammatory response to orchestrate the recruitment
of myeloid cells, but how ETBF recruits colonic myeloid cells remains poorly understood. S1p acts
as bioactive sphingolipid messengers, influencing the myeloid cells migration and regulating
colonic inflammation. However, whether ETBF integrates sphingolipid metabolites to determine
the metabolism of colonic myeloid cells needs to be explored. Recent evidence indicates that
remodeling of myeloid cells metabolism is central to the induction of innate immune response.
We found ETBF infection alters the activity of sphingosine kinase, which is linked to metabolic
remodeling, histone acetylation and PGE2 production in myeloid cells. Two integrated specific
aims are proposed to test: Aim 1 will determine how ETBF infection regulates inflammatory
myeloid cells accumulation in the colon. Aim 2 will determine if ETBF alteration of acetyl-CoA
contributes to metabolic remodeling in myeloid cells via PPARγ activation. Deeper understanding
of the proper role of sphingolipids and their enzymes in controlling the intestinal immune
properties and in promoting the pathogenesis and progression of colitis will generate new
perspectives in the development of “sphingolipid-centered” therapeutic strategies that control the
onset and perpetuation of the ETBF-induced gut inflammation.
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