scholarly journals Regulation of nestin expression by thrombin and cell density in cultures of bone mesenchymal stem cells and radial glial cells

2007 ◽  
Vol 8 (1) ◽  
pp. 104 ◽  
Author(s):  
Franz Wautier ◽  
Sabine Wislet-Gendebien ◽  
Grazyna Chanas ◽  
Bernard Rogister ◽  
Pierre Leprince
2009 ◽  
Vol 67 (3a) ◽  
pp. 684-688 ◽  
Author(s):  
Carla Alessandra Scorza ◽  
Ricardo Mario Arida ◽  
Fulvio Alexandre Scorza ◽  
Esper Abrão Cavalheiro ◽  
Maria da Graça Naffah-Mazzacoratti

OBJECTIVE: Nestin is temporarily expressed in several tissues during development and it is replaced by other protein types during cell differentiation process. This unique property allows distinguishing between undifferentiated and differentiated cells. This study was delineated to analyze the temporal pattern of nestin expression in cortical radial glial cells of rats during normal development and of rats submitted to recurrent status epilepticus (SE) in early postnatal life (P). METHOD: Experimental rats were submitted to pilocarpine-induced SE on P7-9. The cortical temporal profile of nestin was studied by immunohistochemistry at multiple time points (P9, P10, P12, P16, P30 and P90). RESULTS: We observed delayed nestin down-regulation in experimental rats of P9, P10, P12 and P16 groups. In addition, few radial glial cells were still present only in P21 experimental rats. CONCLUSION: Our results suggested that SE during early postnatal life alters normal maturation during a critical period of brain development.


Author(s):  
Nicoletta Kessaris ◽  
Nigel Pringle ◽  
William D Richardson

All the neurons and glial cells of the central nervous system are generated from the neuroepithelial cells in the walls of the embryonic neural tube, the ‘embryonic neural stem cells’. The stem cells seem to be equivalent to the so-called ‘radial glial cells’, which for many years had been regarded as a specialized type of glial cell. These radial cells generate different classes of neurons in a position-dependent manner. They then switch to producing glial cells (oligodendrocytes and astrocytes). It is not known what drives the neuron–glial switch, although downregulation of pro-neural basic helix–loop–helix transcription factors is one important step. This drives the stem cells from a neurogenic towards a gliogenic mode. The stem cells then choose between developing as oligodendrocytes or astrocytes, of which there might be intrinsically different subclasses. This review focuses on the different extracellular signals and intracellular responses that influence glial generation and the choice between oligodendrocyte and astrocyte fates.


Neuron ◽  
2017 ◽  
Vol 95 (2) ◽  
pp. 309-325.e6 ◽  
Author(s):  
Xiao-Ling Hu ◽  
Guo Chen ◽  
Sanguo Zhang ◽  
Jiangli Zheng ◽  
Jun Wu ◽  
...  

2014 ◽  
Vol 94 (3) ◽  
pp. 709-737 ◽  
Author(s):  
Leda Dimou ◽  
Magdalena Götz

The diverse functions of glial cells prompt the question to which extent specific subtypes may be devoted to a specific function. We discuss this by reviewing one of the most recently discovered roles of glial cells, their function as neural stem cells (NSCs) and progenitor cells. First we give an overview of glial stem and progenitor cells during development; these are the radial glial cells that act as NSCs and other glial progenitors, highlighting the distinction between the lineage of cells in vivo and their potential when exposed to a different environment, e.g., in vitro. We then proceed to the adult stage and discuss the glial cells that continue to act as NSCs across vertebrates and others that are more lineage-restricted, such as the adult NG2-glia, the most frequent progenitor type in the adult mammalian brain, that remain within the oligodendrocyte lineage. Upon certain injury conditions, a distinct subset of quiescent astrocytes reactivates proliferation and a larger potential, clearly demonstrating the concept of heterogeneity with distinct subtypes of, e.g., astrocytes or NG2-glia performing rather different roles after brain injury. These new insights not only highlight the importance of glial cells for brain repair but also their great potential in various aspects of regeneration.


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