Selective neuronal silencing to study cognitive decline in Alzheimer's disease
Selective neuronal silencing to study cognitive decline in Alzheimer's disease
批准号:
7677014
负责人:
JOANNA L JANKOWSKY
金额:
$209.21万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-30 至 2012-08-31
关键词:
AddressAdultAlzheimer&aposs DiseaseAnimalsBehavioralBiochemicalCellsChloride ChannelsCommunitiesDiseaseFunctional disorderGoalsHippocampus (Brain)Impaired cognitionImpairmentIvermectinLaboratoriesLearningLinkMemoryMethodsMorphologyMusNeurobiologyNeurodegenerative DisordersNeurologicNeuronsNeurosciencesPartner in relationshipPatientsPopulationProcessRoleSymptomsTechnologyTimeTransgenic MiceTransgenic Organismsmigrationmouse modelneuropathologynovelrecombinase
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Our understanding of neurodegenerative diseases is currently hindered by lack of a firm
neurobiological link between the patient's symptoms and the underlying neuropathology. To
advance, we must identify not only key biochemical changes, but also how these changes alter
the function of specific circuits to cause neurological symptoms. I seek to understand how
impairment of particular circuits initiates early symptoms of Alzheimer¿s disease (AD), and how
addition of further dysfunction leads to the disease's ultimate decline. I will apply a new method
of selective neuronal silencing in transgenic mice to examine the behavioral impact of
inactivating neuronal circuits damaged in AD. My postdoctoral laboratory has developed a
novel chloride channel that responds specifically to ivermectin by producing hyperpolarization
that results in selective, reversible suppression of neuronal activity. I will use my expertise in
transgenic technology to create a mouse in which the ivermectin channel is conditionally
expressed under control of Cre recombinase. Mating this mouse to animals expressing Cre in
selected neuronal populations will allow those cells to be silenced with systemic ivermectin. My
goal is to explore the function of adult-born hippocampal neurons, as this population is severely
diminished in mouse models for AD. I will examine the role of these cells in learning and
memory by selectively silencing them at critical times in the acquisition, consolidation, and recall
of new information. Additional studies will address the effect of silencing on the migration,
morphology, and survival of these adult-born cells. My long-term plans are to examine the
behavioral impact of silencing other circuits damaged later in the course of disease to
understand how diminished activity in multiple domains results in the progressive cognitive
decline of AD. In the process, I will generate a transgenic mouse for selective neuronal
silencing that will be broadly useful to the neuroscience community.
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海外基金