Skip to main content

Neuronal Division and Migration

Neuronal division and migration are critical processes in neurodevelopment that contribute to the formation of the complex structure of the human brain. Here is an explanation of neuronal division and migration:


1.     Neurogenesis: Neurogenesis is the process by which neurons are generated from neural stem cells. It involves a precisely orchestrated sequence of cellular events that begin with the formation of the neocortex at the rostral end of the neural tube during embryonic development. In humans, the neural tube closes around the fifth week of gestation, marking the initiation of rapid brain enlargement.


2.     Cellular Events: During neurogenesis, neural stem cells divide and differentiate into neurons through asymmetric and symmetric cell divisions. Asymmetric cell divisions produce one stem cell and one progenitor cell or neuron, while symmetric divisions generate two identical daughter cells. These divisions lead to a notable radial and tangential expansion of proliferative zones in the developing brain.


3.     Neuronal Migration: After being generated, neurons undergo migration to their final destinations within the brain. Radial migration is a process where neurons move from the ventricular zone to the outer layers of the cortex along radial glial fibers. This process is crucial for establishing the layered structure of the cerebral cortex. Tangential migration involves the movement of neurons parallel to the brain's surface and contributes to the diversification of neuronal types and the formation of neural circuits.


4.     Subventricular Zone: The subventricular zone plays a key role in coordinating the migration of pyramidal neurons and interneurons during brain development. Neurons pause in the subventricular zone before migrating radially, suggesting a synchronization mechanism for neuronal migration. Early-born cells in the preplate, a transient structure near the basal surface, will either migrate tangentially to become inhibitory interneurons or die during early neurogenesis.


5.     Intracranial Pressure: Intracranial pressure, regulated by the ventricular system and cerebrospinal fluid dynamics, is recognized as an important regulator of normal brain development. Changes in intracranial pressure can impact brain enlargement, tissue organization, and folding patterns during neurodevelopment.

In summary, neuronal division and migration are fundamental processes in neurodevelopment that shape the structure and connectivity of the human brain. Understanding the mechanisms underlying these processes is essential for unraveling the complexities of brain development and the pathogenesis of neurological disorders.
 

Comments

Popular posts from this blog

How do pharmacological interventions targeting NMDA glutamate receptors and PKCc affect alcohol drinking behavior in mice?

Pharmacological interventions targeting NMDA glutamate receptors and PKCc can have significant effects on alcohol drinking behavior in mice. In the context of the study discussed in the PDF file, the researchers investigated the impact of these interventions on ethanol-preferring behavior in mice lacking type 1 equilibrative nucleoside transporter (ENT1). 1.   NMDA Glutamate Receptor Inhibition : Inhibition of NMDA glutamate receptors can reduce ethanol drinking behavior in mice. This suggests that NMDA receptor-mediated signaling plays a role in regulating alcohol consumption. By blocking NMDA receptors, the researchers were able to observe a decrease in ethanol intake in ENT1 null mice, indicating that NMDA receptor activity is involved in the modulation of alcohol preference. 2.   PKCc Inhibition : Down-regulation of intracellular PKCc-neurogranin (Ng)-Ca2+-calmodulin dependent protein kinase type II (CaMKII) signaling through PKCc inhibition is correlated with reduced CREB activity

How the Neural network circuits works in Parkinson's Disease?

  In Parkinson's disease, the neural network circuits involved in motor control are disrupted, leading to characteristic motor symptoms such as tremor, bradykinesia, and rigidity. The primary brain regions affected in Parkinson's disease include the basal ganglia and the cortex. Here is an overview of how neural network circuits work in Parkinson's disease: 1.      Basal Ganglia Dysfunction: The basal ganglia are a group of subcortical nuclei involved in motor control. In Parkinson's disease, there is a loss of dopamine-producing neurons in the substantia nigra, leading to decreased dopamine levels in the basal ganglia. This dopamine depletion results in abnormal signaling within the basal ganglia circuitry, leading to motor symptoms. 2.      Cortical Involvement: The cortex, particularly the motor cortex, plays a crucial role in initiating and coordinating voluntary movements. In Parkinson's disease, abnormal activity in the cortex, especially in the beta and gamma

Force-Velocity Relationship

The force-velocity relationship in muscle physiology describes how the force a muscle can generate is influenced by the velocity of muscle contraction. Here are key points regarding the force-velocity relationship: 1.     Inverse Relationship : o     The force-velocity relationship states that the force a muscle can generate is inversely related to the velocity of muscle shortening. o     At higher contraction velocities (faster shortening), the force-generating capacity of the muscle decreases. o     Conversely, at lower contraction velocities (slower shortening), the muscle can generate higher forces. 2.     Factors Influencing Force-Velocity Relationship : o     Cross-Bridge Cycling : The rate at which cross-bridges form and detach during muscle contraction affects the force-velocity relationship. At higher velocities, there is less time for cross-bridge formation, leading to reduced force production. o     Energy Availability : The availability of ATP, which powers muscle contracti

How can a better understanding of the physical biology of brain development contribute to advancements in neuroscience and medicine?

A better understanding of the physical biology of brain development can significantly contribute to advancements in neuroscience and medicine in the following ways: 1.    Insights into Neurodevelopmental Disorders:  Understanding the role of physical forces in brain development can provide insights into the mechanisms underlying neurodevelopmental disorders. By studying how disruptions in mechanical cues affect brain structure and function, researchers can identify new targets for therapeutic interventions and diagnostic strategies for conditions such as autism, epilepsy, and intellectual disabilities. 2.   Development of Novel Treatment Approaches:  Insights from the physical biology of brain development can inspire the development of novel treatment approaches for neurological disorders. By targeting the mechanical aspects of brain development, such as cortical folding or neuronal migration, researchers can design interventions that aim to correct abnormalities in brain structure and

Complex Random Sampling Designs

Complex random sampling designs refer to sampling methods that involve a combination of various random sampling techniques to select a sample from a population. These designs often incorporate elements of both probability and non-probability sampling methods to achieve specific research objectives. Here are some key points about complex random sampling designs: 1.     Definition : o     Complex random sampling designs involve the use of multiple random sampling methods, such as systematic sampling, stratified sampling, cluster sampling, etc., in a structured manner to select a sample from a population. o     These designs aim to improve the representativeness, efficiency, and precision of the sample by combining different random sampling techniques. 2.     Purpose : o    The primary goal of complex random sampling designs is to enhance the quality of the sample by addressing specific characteristics or requirements of the population. o     Researchers may use these designs to increase