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Neurulation
Phase after gastrulation forming the neural tube from mesoderm, ectoderm, and endoderm.
Neural precursor cells
Pluripotent cells giving rise to neurons, controlled by signal molecules and transcription factors.
Neural plate
Earliest nervous system formation at 18 days, triggered by mesoderm and ectoderm contact.
Neural tube
Forms at 22 days from additional folding of the neural plate, crucial for early neuron development.
Prosencephalon
Brain region giving rise to the forebrain, part of the regional brain specification during development.
Retinoic acid (RA)
Inducer of early nervous system development, released from floor and roof plates.
Growth cone
Specialized structure at axon tips guiding axon growth and responding to chemoattraction and chemorepulsion.
Lamellipodium
Large flat extension of axon involved in growth cone structure and axon elongation.
Filopodium
Fine extensions of the lamellipodium, crucial for sensing environmental signals in growth cones.
Cell signaling
Major role in shaping growth cones and axon growth, influenced by diffusible and non-diffusible molecules.
Voltage-gated ion channels
Channels that open or close in response to changes in membrane potential
TRP channels
Ion channels activated by second messengers, like Ca2+, involved in sensory transduction
Chemoattraction
Signals that selectively attract growth cones to specific destinations
Chemorepulsion
Signals that discourage axon growth towards inappropriate targets
Integrin
Non-diffusible factor that mediates cell adhesion to the extracellular matrix
Netrin function
Attractive secreted signals that stimulate growth cone extension via specific receptors
Semaphorin function
Repulsive cues that prevent axon extension by modifying growth cone cytoskeleton
Tropic molecules
Guide axons towards specific sources or destinations
Trophic molecules
Support the survival and growth of neurons and their processes
Topographic map formation
Development of maps based on gradients of molecules that guide axon growth
Integrated networks
Networks of signal molecules and transcription factors controlling neuronal development
Synapse formation initiation
Process involving local recognition between pre- and postsynaptic membranes
Synapse identity development
Differentiation of active zones and postsynaptic density after initial synapse formation
Neurotrophic factors
Factors like NGF and BDNF that regulate neuronal growth, survival, and differentiation
Competition in synapse formation
Process where synapse elimination is modulated by electrical activation and competition
Tyrosine kinase receptors (Trk)
Receptors activated by neurotrophins, regulating cell signaling pathways
Nerve regeneration steps
Process involving degeneration, growth cone formation, and interaction with Schwann cells
Schwann cells in nerve regeneration
Cells that provide molecular support and secrete ECM molecules to facilitate axon regrowth
Motor endplate fate
Fate of the neuromuscular junction after severing the innervating nerve
Role of BDNF and NGF in reinnervation
Enhance tropic and trophic signaling for target recognition and synaptogenesis
Activity in regenerating axons
Activity-dependent mechanisms that influence synapse re-formation during regeneration
Nerve graft
Use of peripheral nerve grafts containing Schwann cells to facilitate nerve regeneration
Glial scarring
Inhibition of CNS regeneration due to the formation of glial scars
Regeneration in the olfactory nerve
Ability of axons to regenerate in the olfactory nerve despite CNS regeneration inhibition
Neurogenesis
The process of generating new nerve cells in the adult vertebrate brain, including humans.
Stem niches
Specialized regions in the adult brain of vertebrates and humans that support the maintenance of stem cells, regulated by neurotrophins and neurotrophin receptors.
Neuroblast migration
Movement of neuroblasts from stem cell niches to their target regions in the brain.
Apoptosis
Programmed cell death mechanism in which cells self-destruct.
Glial scar
Formation of scar tissue in the brain due to the proliferation of glial cells, hindering axon growth.
Excitotoxicity
Mechanism of neuronal cell death caused by elevated neuronal activity due to glutamate release.
NoGo-A
Protein secreted in glial scars that inhibits neurite outgrowth and axon regeneration.
Astrocyte
Glial cell type that produces molecules inhibiting axon growth and promotes glial scarring.
Microglia
Glial cells that clear debris, release inhibitory factors, and hinder axon growth in the CNS.
Olfactory ensheathing cells
Cells that stimulate axon regeneration when injected into the brain, particularly in the olfactory nerve.
Liraglutide Function
Liraglutide is a medication used to treat obesity by reducing appetite and promoting weight loss.
Liraglutide Mechanism
Liraglutide acts by targeting neurons in the hypothalamus to lower appetite.
Hypothalamic Neurons
Liraglutide primarily affects or regulates neurons in the hypothalamus.
Liraglutide and Adipose Tissue
Liraglutide leads to the reduction of adipose tissue and body weight loss through its actions on the hypothalamus.
Neuronal Access
Liraglutide can access neurons in the hypothalamus to exert its effects.
GLP-1 Receptor Role
The GLP-1 Receptor plays a crucial role in regulating food intake and appetite control.