THESIS
2018
ix, 43 pages : illustrations (some color) ; 30 cm
Abstract
Microglia are resident macrophages in central nervous system (CNS) playing pivotal
roles in supporting neuron development by pruning synapses and secreting neuron
trophic factors as well as keeping brain homeostasis by clearing dead neurons and Aβ
plaques. It is well accepted that microglia are highly associated with Alzheimer’s
disease, Parkinson’s disease and prion disease. Comprehensive and thorough
understanding of microglial development and function is beneficial to realize the
causes of neurodegenerative diseases and seek for novel strategies for treatment.
However, the molecular mechanism of how microglia develop and maintain
homeostasis in brain is still largely unknown. Here, in our study, a temperature
sensitive mutant named puer was identified by ENU-induced forward...[
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Microglia are resident macrophages in central nervous system (CNS) playing pivotal
roles in supporting neuron development by pruning synapses and secreting neuron
trophic factors as well as keeping brain homeostasis by clearing dead neurons and Aβ
plaques. It is well accepted that microglia are highly associated with Alzheimer’s
disease, Parkinson’s disease and prion disease. Comprehensive and thorough
understanding of microglial development and function is beneficial to realize the
causes of neurodegenerative diseases and seek for novel strategies for treatment.
However, the molecular mechanism of how microglia develop and maintain
homeostasis in brain is still largely unknown. Here, in our study, a temperature
sensitive mutant named puer was identified by ENU-induced forward genetic
screening. Genetic mapping and mRNA rescue assays confirmed that nlrc3-like
carrying a T to A mutation in coding sequence, a member of NOD-like receptor
family, is the causative gene to microglia defect. Further time-lapse imaging with
temperature shift assays illustrated that microglia undergo pyroptotic cell death and
inflammatory activation after colonization into brain. Besides, disruption of pycard
partially prevents the microglia cell death in puer mutant under restricted temperature.
Taken together, nlrc3-like maintains microglia homeostasis by preventing them from
pycard-dependent pyroptosis.
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