The role of gut endocrine cells in Parkinson's Disease
The role of gut endocrine cells in Parkinson's Disease
批准号:
9756369
负责人:
Rodger A. Liddle
金额:
$35.78万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-01 至 2021-08-31
关键词:
ApicalAxonBrainBrain DiseasesCell Surface ReceptorsCellsCommunicationDataDigestionDiseaseEatingEnteralEnterocytesEnteroendocrine CellEnvironmentEnvironmental ExposureEpidemiologyEpithelial CellsExposure toFoodFutureGastrointestinal tract structureGut MucosaHerbicidesIngestionInjuryIntestinesLewy BodiesMolecularNervous system structureNeurodegenerative DisordersNeuronsParaquatParkinson DiseasePathogenesisPathway interactionsPatientsPesticidesProcessProteinsRabies virusRoleRotenoneSecretory VesiclesSensorySignal TransductionSourceSurfaceSynapsesSynaptic VesiclesTestingTissuesToxicant exposurealpha synucleingastrointestinal epitheliumgut endocrine cellinsightneurofilamentnovelpathogenpresynaptic neuronsprion-likeprotein aggregatepublic health relevancerelating to nervous systemtoxicantvesicular release
中文摘要
描述(由申请人提供):肠内分泌细胞(EECs)是胃肠道的感觉细胞。它们的顶端表面向肠腔开放,基底外侧表面含有丰富的分泌囊泡,这些囊泡在细胞受到刺激时释放出来。通过特定的细胞表面受体,EECs在食物通过肠道时感知食物。我们最近发现,肠道的脑脊液具有许多神经元样的特征,包括被称为神经足的轴突样过程。正是通过神经足,脑电图细胞与神经元相连。这种神经连接提供了从肠道到大脑的直接交流,也是大脑感知肠管内容物的方式。胃肠道通过食物不断暴露于环境中,有时食物中含有除草剂和杀虫剂,肠道黏膜中的eec是除草剂暴露的现成目标。流行病学和实验数据表明,环境暴露于除草剂和杀虫剂是帕金森病的主要原因。帕金森病的特点是神经元内路易小体由α-突触核蛋白聚集而成,α-突触核蛋白是一种可以防止毒性损伤的神经元蛋白。α-突触核蛋白的聚集体可以在细胞间传递,诱导聚集体形成“类似朊病毒的级联”,在神经系统中扩散。异常α-突触核蛋白在扩散到大脑之前出现在肠神经元中。因此,帕金森氏症发生在神经组织与环境非常接近的区域,如肠道,尽管这是如何发生的尚不清楚。在它们的神经元样特征中,我们发现EECs也表达α-突触核蛋白。这一发现提出了脑脊液是帕金森病来源的可能性。我们认为杀虫剂和除草剂导致EECs中α-突触核蛋白异常,并将α-突触核蛋白传递到肠道神经元并扩散到神经系统。我们将通过确定已知导致帕金森病的除草剂和杀虫剂是否在EECs中产生异常的α-突触核蛋白,以及EECs是否将折叠的α-突触核蛋白传递给神经元来验证这一假设。这些研究将确定EECs是否是异常α-突触核蛋白的来源,异常α-突触核蛋白可能是帕金森病的起源。确定帕金森病的来源可能为未来的治疗提供新的靶点。
英文摘要
DESCRIPTION (provided by applicant): Enteroendocrine cells (EECs) are sensory cells of the gastrointestinal tract. Their apical surface is open to the lumen of the intestine and their basolateral surface contains abundant secretory vesicles that are released upon stimulation of the cell. Through specific cell surface receptors, EECs sense food as it passes through the intestine. We recently discovered that EECs of the gut possess many neuron-like features including axon-like processes known as neuropods. It is through neuropods that EECs connect to neurons. This neural connection provides a direct communication from the gut to the brain and is how the brain senses luminal contents. The gastrointestinal tract is constantly exposed to the environment through food that sometimes harbors herbicides and pesticides and EECs in the gut mucosa are ready targets for herbicide exposure. Epidemiological and experimental data indicate that environmental exposure to herbicides and pesticides is a major cause of Parkinson's disease. Parkinson's disease is characterized by intraneuronal Lewy bodies that consist of aggregates of α-synuclein, a neuronal protein that may protect against toxic injury. Aggregates of α-synuclein can be passed from cell to cell, inducing aggregates in a "prion-like cascade" that spreads through the nervous system. Abnormal α-synuclein appears in enteric neurons before it spreads to the brain. Therefore, Parkinson's disease arises in regions where neural tissues are in close proximity to the environment, such as the gut, although how this occurs is unknown. Among their neuron-like features we discovered that EECs also express α-synuclein. This finding raises the possibility that EECs are the source of Parkinson's disease. We propose that pesticides and herbicides cause abnormal α-synuclein in EECs that is transmitted to neurons in the gut and spreads to the nervous system. We will test this hypothesis by determining if herbicides and pesticides known to cause Parkinson's disease produce abnormal α-synuclein in EECs and if EECs transmit is folded α-synuclein to neurons. These studies will determine if EECs are the source of abnormal α-synuclein that could be the origin of Parkinson's disease. Identifying the source of Parkinson's disease may offer new targets for future therapy.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.jcmgh.2016.10.005
发表时间:
2017
期刊:
Cellular and molecular gastroenterology and hepatology
影响因子:
7.2
作者:
[Liddle,RodgerA]
通讯作者:
Liddle,RodgerA
Mechanisms of Pancreatic Fibrosis
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批准号:10265587
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项目类别:
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资助金额:$36.23万
-
财政年份:2020
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负责人:Rodger A. Liddle
-
依托单位:
Mechanisms of Pancreatic Fibrosis
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批准号:10118457
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项目类别:
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资助金额:$35.95万
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财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Mechanisms of Pancreatic Fibrosis
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批准号:10630177
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项目类别:
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资助金额:$36.23万
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财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Metabolic regulation of pancreatitis
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批准号:10353436
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项目类别:
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资助金额:$36.23万
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财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Metabolic regulation of pancreatitis
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批准号:10028137
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项目类别:
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资助金额:$36.23万
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财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Metabolic regulation of pancreatitis
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批准号:10187560
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项目类别:
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资助金额:$36.23万
-
财政年份:2020
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负责人:Rodger A. Liddle
-
依托单位:
Mechanisms of Pancreatic Fibrosis
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批准号:10408830
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项目类别:
-
资助金额:$36.23万
-
财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Metabolic regulation of pancreatitis
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批准号:10559568
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项目类别:
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资助金额:$36.23万
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财政年份:2020
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负责人:Rodger A. Liddle
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依托单位:
Mechanisms of mechanically-induced acute pancreatitis
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批准号:10538561
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项目类别:
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资助金额:$36.23万
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财政年份:2019
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负责人:Rodger A. Liddle
-
依托单位:
Mechanisms of mechanically-induced acute pancreatitis
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批准号:10320376
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项目类别:
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资助金额:$36.23万
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财政年份:2019
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负责人:Rodger A. Liddle
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依托单位:
The role of gut endocrine cells in Parkinson's Disease
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批准号:9234533
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项目类别:
-
资助金额:$35.78万
-
财政年份:2016
-
负责人:Rodger A. Liddle
-
依托单位:
The role of gut endocrine cells in Parkinson's Disease
-
批准号:9083432
-
项目类别:
-
资助金额:$35.78万
-
财政年份:2016
-
负责人:Rodger A. Liddle
-
依托单位:
Gut Neuroendocrine Cell Signaling
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批准号:10292431
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项目类别:
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资助金额:$0.0万
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财政年份:2014
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负责人:Rodger A. Liddle
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依托单位:
Gut Neuroendocrine Cell Signaling and Obesity
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批准号:9339527
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项目类别:
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资助金额:$0.0万
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财政年份:2014
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负责人:Rodger A. Liddle
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依托单位:
Gut Neuroendocrine Cell Signaling
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批准号:10045947
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项目类别:
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资助金额:$0.0万
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财政年份:2014
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负责人:Rodger A. Liddle
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依托单位:
Gut Neuroendocrine Cell Signaling
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批准号:9564273
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项目类别:
-
资助金额:$0.0万
-
财政年份:2014
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负责人:Rodger A. Liddle
-
依托单位:
Gut Neuroendocrine Cell Signaling and Obesity
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批准号:8635645
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项目类别:
-
资助金额:$0.0万
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财政年份:2014
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负责人:Rodger A. Liddle
-
依托单位:
Receptor Regulation of CCK Cell Function
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批准号:8623648
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项目类别:
-
资助金额:$34.15万
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财政年份:2013
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负责人:Rodger A. Liddle
-
依托单位:
Receptor Regulation of CCK Cell Function
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批准号:8918605
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项目类别:
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资助金额:$34.15万
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财政年份:2013
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负责人:Rodger A. Liddle
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依托单位:
Receptor Regulation of CCK Cell Function
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批准号:9133365
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项目类别:
-
资助金额:$34.15万
-
财政年份:2013
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负责人:Rodger A. Liddle
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依托单位:
海外基金