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Related Concept Videos

Cell Migration01:09

Cell Migration

Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.
Cell Migration01:19

Cell Migration

Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
Cytoskeletal Coordination in Cell Migration01:32

Cytoskeletal Coordination in Cell Migration

A migrating cell changes its shape during the cyclic events of attachment and detachment from the substratum and repositions the cell organelles correspondingly. These complex events are orchestrated by the dynamic cytoskeletal network comprising actin filaments, intermediate filaments, and microtubules. Cytoskeletal crosstalk — the direct and indirect communication between the different components — is crucial for this coordination. Direct communication involves various linker proteins that...
Gastrulation01:56

Gastrulation

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Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the anterior...

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Related Experiment Video

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Time-Lapse Imaging of Migrating Neurons and Glial Progenitors in Embryonic Mouse Brain Slices
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Cell migration along the lateral cortical stream to the developing basal telencephalic limbic system.

Rosalind S E Carney1, Teresa B Alfonso, Daniela Cohen

  • 1Department of Neuroscience, Georgetown University Medical Center, Washington, DC 20057, USA.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|November 10, 2006
PubMed
Summary

The lateral cortical stream (LCS) arises from the corticostriatal border during development. This study reveals distinct cell origins and migratory patterns within the LCS, highlighting the crucial role of the Gsh2 gene in its formation.

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genetics

Background:

  • The lateral cortical stream (LCS) is a crucial migratory pathway during brain development, originating from the corticostriatal border (CSB).
  • The LCS comprises diverse neural progenitor cells migrating to form key basal telencephalon structures like the piriform cortex and amygdala.

Purpose of the Study:

  • To investigate the timing, cellular composition, migratory behaviors, and genetic requirements of LCS development.
  • To elucidate the role of the transcription factor Gsh2 (genomic screened homeobox 2) in LCS formation.

Main Methods:

  • Employed a combination of in vitro and in vivo experimental approaches.
  • Utilized genetic markers such as Pax6 and Dlx2 to distinguish cell populations.
  • Analyzed cell origins, migratory routes, and gene dependencies.

Main Results:

  • Identified distinct temporal windows for the generation of Pax6-positive (pallial) and Dlx2-positive (subpallial) LCS progenitor cells.
  • Revealed the CSB as a source of both distinct and co-expressing Pax6/Dlx2 progenitor populations.
  • Demonstrated that Dlx2-positive cells exhibit chain-like migration and are generated locally at the CSB.
  • Established that LCS generation is dependent on the homeobox gene Gsh2.

Conclusions:

  • The development of the LCS involves temporally regulated, distinct progenitor populations originating from the CSB.
  • Gsh2 plays a novel and essential role in the formation of the LCS and overall telencephalic development.