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'''Neurosphere'''
{{Short description|A cluster of neural stem cells used in research}}


A '''neurosphere''' is a culture system composed of neural stem cells and progenitor cells which are capable of self-renewal and limited lineage potential. The neurosphere assay (NSA) is a common method used to study these cells.
==Neurosphere==
A '''neurosphere''' is a culture system composed of free-floating clusters of neural stem cells (NSCs). These clusters are used extensively in [[neuroscience]] research to study the properties of NSCs, including their ability to proliferate, differentiate, and self-renew. Neurospheres provide a valuable in vitro model for understanding the development and potential therapeutic applications of neural stem cells.


== History ==
[[File:Neurosphere.jpg|thumb|right|A neurosphere under a microscope, showing a cluster of neural stem cells.]]


The neurosphere was first described by Reynolds and Weiss in 1992. They discovered that when dissociated cells from the striatum of the adult mouse brain were cultured in serum-free medium containing epidermal growth factor (EGF), a small proportion of the cells survived and proliferated to form clusters of cells, which they termed neurospheres.
==Formation==
Neurospheres are formed when neural stem cells are cultured in a medium that supports their growth and prevents their attachment to the substrate. This is typically achieved by using a serum-free medium supplemented with growth factors such as [[epidermal growth factor]] (EGF) and [[fibroblast growth factor]] (FGF). Under these conditions, NSCs proliferate and form spherical clusters, or neurospheres, which can be maintained and expanded over several passages.


== Characteristics ==
==Properties==
Neurospheres exhibit several key properties that make them useful for research:


Neurospheres are characterized by their ability to maintain multipotentiality, which means they can differentiate into neurons, astrocytes, and oligodendrocytes. They are also capable of self-renewal, meaning they can generate new neurospheres from single cells.
* '''Self-renewal''': The cells within a neurosphere can divide and produce more stem cells, maintaining the population over time.
* '''Multipotency''': NSCs within neurospheres have the potential to differentiate into various cell types found in the [[central nervous system]], including [[neurons]], [[astrocytes]], and [[oligodendrocytes]].
* '''Clonality''': Neurospheres can be derived from a single NSC, allowing researchers to study the properties of individual stem cells and their progeny.


== Neurosphere Assay (NSA) ==
==Applications==
Neurospheres are used in a variety of research applications, including:


The neurosphere assay (NSA) is a method used to quantify neural stem and progenitor cells in vitro. It is based on the ability of neural stem cells to proliferate and form neurospheres in the presence of growth factors such as EGF and fibroblast growth factor 2 (FGF2).
* '''Neurodevelopmental studies''': Neurospheres provide a model to study the processes involved in the development of the nervous system.
* '''Disease modeling''': Researchers use neurospheres to model neurological diseases and disorders, such as [[Parkinson's disease]] and [[Alzheimer's disease]], to better understand their pathophysiology.
* '''Drug screening''': Neurospheres can be used to test the effects of potential therapeutic compounds on neural stem cells and their differentiated progeny.
* '''Regenerative medicine''': Neurospheres are explored as a source of cells for regenerative therapies aimed at repairing damaged or diseased nervous tissue.


== Criticisms ==
[[File:Neural differentiation.jpg|thumb|left|Differentiation of neural stem cells into neurons and glial cells.]]


Despite its widespread use, the NSA has been criticized for its lack of specificity and reproducibility. Some researchers argue that the number of neurospheres formed in the NSA does not accurately reflect the number of stem cells in a given population, as the assay is also influenced by progenitor cell proliferation and survival.
==Challenges==
While neurospheres are a powerful tool for research, they also present certain challenges:


== See also ==
* '''Heterogeneity''': Neurospheres can be heterogeneous, containing a mix of stem cells and differentiated cells, which can complicate data interpretation.
* '''Standardization''': Variability in culture conditions and techniques can lead to inconsistent results between different laboratories.
* '''In vivo relevance''': While neurospheres provide a useful in vitro model, translating findings to in vivo systems remains a significant challenge.


==Related pages==
* [[Neural stem cell]]
* [[Neural stem cell]]
* [[Stem cell therapy]]
* [[Neurogenesis]]
* [[Neurogenesis]]
* [[Epidermal growth factor]]
* [[Cell culture]]
* [[Fibroblast growth factor 2]]
 
== References ==
 
<references />


[[Category:Stem cells]]
[[Category:Neuroscience]]
[[Category:Neuroscience]]
[[Category:Cell biology]]
[[Category:Stem cells]]
{{stub}}
{{dictionary-stub1}}
<gallery>
File:Journal.pone.0001604.g001_small.jpg|Neurosphere
File:Reynolds_and_Weiss_Neurosphere_1992.jpg|Neurosphere
File:Neuroshperes_with_ZIKV_infection.jpg|Neurosphere
</gallery>

Revision as of 17:44, 18 February 2025

A cluster of neural stem cells used in research


Neurosphere

A neurosphere is a culture system composed of free-floating clusters of neural stem cells (NSCs). These clusters are used extensively in neuroscience research to study the properties of NSCs, including their ability to proliferate, differentiate, and self-renew. Neurospheres provide a valuable in vitro model for understanding the development and potential therapeutic applications of neural stem cells.

File:Neurosphere.jpg
A neurosphere under a microscope, showing a cluster of neural stem cells.

Formation

Neurospheres are formed when neural stem cells are cultured in a medium that supports their growth and prevents their attachment to the substrate. This is typically achieved by using a serum-free medium supplemented with growth factors such as epidermal growth factor (EGF) and fibroblast growth factor (FGF). Under these conditions, NSCs proliferate and form spherical clusters, or neurospheres, which can be maintained and expanded over several passages.

Properties

Neurospheres exhibit several key properties that make them useful for research:

  • Self-renewal: The cells within a neurosphere can divide and produce more stem cells, maintaining the population over time.
  • Multipotency: NSCs within neurospheres have the potential to differentiate into various cell types found in the central nervous system, including neurons, astrocytes, and oligodendrocytes.
  • Clonality: Neurospheres can be derived from a single NSC, allowing researchers to study the properties of individual stem cells and their progeny.

Applications

Neurospheres are used in a variety of research applications, including:

  • Neurodevelopmental studies: Neurospheres provide a model to study the processes involved in the development of the nervous system.
  • Disease modeling: Researchers use neurospheres to model neurological diseases and disorders, such as Parkinson's disease and Alzheimer's disease, to better understand their pathophysiology.
  • Drug screening: Neurospheres can be used to test the effects of potential therapeutic compounds on neural stem cells and their differentiated progeny.
  • Regenerative medicine: Neurospheres are explored as a source of cells for regenerative therapies aimed at repairing damaged or diseased nervous tissue.
File:Neural differentiation.jpg
Differentiation of neural stem cells into neurons and glial cells.

Challenges

While neurospheres are a powerful tool for research, they also present certain challenges:

  • Heterogeneity: Neurospheres can be heterogeneous, containing a mix of stem cells and differentiated cells, which can complicate data interpretation.
  • Standardization: Variability in culture conditions and techniques can lead to inconsistent results between different laboratories.
  • In vivo relevance: While neurospheres provide a useful in vitro model, translating findings to in vivo systems remains a significant challenge.

Related pages