Understanding Phagocytosis Within the Adipose Tissue
Understanding Phagocytosis Within the Adipose Tissue
批准号:
10557389
负责人:
Brady Barron
金额:
$3.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-09-01 至 2023-08-01
关键词:
ANXA5 geneAddressAdipocytesAdipose tissueAdultAffectApoptosisApoptoticBiological AssayCRISPR/Cas technologyCell DeathCell physiologyCellsCessation of lifeCoupledDataDendritic CellsDevelopmentDiabetes MellitusDiseaseEmbryoEpithelial CellsFatty acid glycerol estersGastrointestinal tract structureGenesGoalsHigh Fat DietHomeostasisHumanHypertrophyImmuneImmune systemIn VitroIndividualInfiltrationInflammationInflammatoryInsulinInsulin ResistanceKnock-outKnockout MiceLeadLimb DevelopmentLipidsLungMaintenanceMesenchymalMethodsMolecularMusNecrosisNon-Insulin-Dependent Diabetes MellitusObesityPathogenesisPathologyPhagocytesPhagocytosisPhosphatidylserinesPlayPopulationProcessProductionProteinsReportingResolutionRoleSecondary toStressSurfaceTNF geneTestingTherapeuticUnited StatesVisceralWeight Gainadipocyte differentiationbasecell typecomorbiditydiabetes mellitus therapyfeedingimprovedin vivoinhibitorinsulin sensitivitylipid biosynthesismacrophagenovelobesity developmentphosphatidylserine receptorpreventstem cellssubcutaneous
中文摘要
项目总结/摘要
每天,我们周转数十亿个凋亡细胞,这些细胞被吞噬细胞清除,如
巨噬细胞细胞死亡和吞噬清除过程对维持体内平衡至关重要,
与许多疾病病理学有关。据报道,脂肪组织经历基础周转,并且在
在肥胖症的情况下,凋亡脂肪细胞已显示在小鼠和人中增加。这种细胞死亡和
随后巨噬细胞浸润以清除垂死细胞被描述为炎症的关键诱导物,
导致胰岛素抵抗的发展。这种炎症特别归因于巨噬细胞
活性,因为巨噬细胞的消耗减少了炎症并提高了胰岛素敏感性。有趣的是,这些
巨噬细胞耗竭条件不导致死细胞的积累,可能证明了额外的
吞噬细胞群。除了专职吞噬细胞(如巨噬细胞),
也存在吞噬细胞,例如消化道和肺中的上皮细胞,或胚胎发育期间的间充质细胞。
肢体发育这些非专职吞噬细胞在维持体内平衡方面发挥着重要作用,但在
脂肪组织迄今为止还没有定义这样的群体。根据初步研究,我们建议调查
脂肪组织中特定的非专职吞噬细胞群,并确定这些细胞如何有助于
炎症、炎症消退和与肥胖相关的胰岛素抵抗。PtdSer是一种特定的脂质
暴露在凋亡细胞的表面上,并被吞噬细胞用于清除。让我们更好地
操纵这些细胞群的吞噬活性,我们将另外研究
磷脂酰丝氨酸(PtdSer)受体。了解细胞类型、吞噬过程和分子参与者
在体内平衡和脂肪组织炎症期间将为肥胖提供重要的治疗机会。
英文摘要
PROJECT SUMMARY/ABSTRACT
On a daily basis, we turnover billions of apoptotic cells that are removed by phagocytic cells, such as
macrophages. The processes of cell death and phagocytic clearance are vital to maintaining homeostasis and are
related to many disease pathologies. The adipose tissue has been reported to undergo basal turnover, and during
conditions of obesity, apoptotic adipocytes have been shown to increase in mice and humans. This cell death and
subsequent macrophage infiltration to clear the dying cells has been described as a key inducer of inflammation and
causative in the development of insulin resistance. This inflammation has been specifically attributed to macrophage
activity, as depletion of macrophages reduces inflammation and improves insulin sensitivity. Interestingly, these
macrophage depletion conditions do not result in the accumulation of dead cells, possibly demonstrating additional
phagocytic population(s). In addition to professional phagocytes (such as macrophages), non-professional
phagocytes also exist, such as epithelial cells in the digestive tract and lung, or mesenchymal cells during embryonic
limb development. These non-professional phagocytes can play vital roles in maintaining homeostasis, yet in the
adipose tissue no such population has been defined thus far. Based on preliminary studies, we propose to investigate
specific non-professional phagocytic cell populations in the adipose tissue and define how these cells contribute to
inflammation, inflammation resolution, and insulin resistance associated with obesity. PtdSer is a lipid specifically
exposed on the surface of apoptotic cells and is used by phagocytic cells for clearance. To allows us to better
manipulate the phagocytic activity of these cell populations, we will additionally investigate the role of
phosphatidylserine (PtdSer) receptors. Understanding cell types, the phagocytic process, and molecular players
during homeostasis and adipose tissue inflammation will provide important therapeutic opportunities for obesity.
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Understanding Phagocytosis Within the Adipose Tissue
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批准号:10251932
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项目类别:
-
资助金额:$3.45万
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财政年份:2020
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负责人:Brady Barron
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依托单位:
海外基金