๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Neural progenitor cells and developmental disorders

โœ Scribed by Mehler, Mark F. ;Kessler, John A.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
105 KB
Volume
4
Category
Article
ISSN
1080-4013

No coin nor oath required. For personal study only.

โœฆ Synopsis


Neural stem/multipotent progenitor cells are present within periventricular generative zones along the entire neuraxis throughout neural development and during adult life. These cells give rise to all of the major cellular elements of the brain, including neurons, oligodendroglia, and astrocytes. Recent studies suggest that cells with a similarly broad lineage potential are also present in postmigratory domains of the postnatal and the adult cerebral cortex. Neural stem cells are defined by a number of properties, including their ability to undergo constitutive proliferation, to maintain themselves (self-renew), to generate large numbers of progeny through transient amplification of intermediate progenitor pools, and to generate new cells in response to injury or disease. These primordial neural cells undergo progressive lineage restriction and commitment to specific neuronal and glial phenotypes in response to cascades of cytokines and the induction of positive and negative transcriptional regulators. These cytokines regulate a range of interrelated cellular processes, including activation, proliferation, viability, lineage commitment, and progressive stages of neuronal and glial lineage maturation. The detailed definition of developmental pathways responsible for neurogenesis and gliogenesis in the mammalian brain will further our understanding of the molecular and cellular basis of mental retardation and other pervasive neurologic disorders of childhood. Further, these cumulative studies suggest that a broad array of neural regenerative strategies, including gene and progenitor cell replacement and activation of endogenous cellular populations, may allow structural and functional reconstitution of neural circuits damaged as a consequence of a spectrum of neurodevelopmental disorders.

1998 Wiley-Liss, Inc.


๐Ÿ“œ SIMILAR VOLUMES


Developmental changes in progenitor cell
โœ G. Zhu; M.F. Mehler; P.C. Mabie; J.A. Kessler ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 288 KB ๐Ÿ‘ 1 views

Multipotent progenitor cells have been identified within periventricular generative zones of the developing and adult brain. To determine whether the environmental responsiveness of these cells changes during development, progenitor cells were cultured from embryonic, postnatal, and adult rat brain

Developmental changes in neural progenit
โœ G. Zhu; M.F. Mehler; P.C. Mabie; J.A. Kessler ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 346 KB ๐Ÿ‘ 1 views

Multipotent neural progenitor cells become progressively more biased towards a glial fate during development coincident with an increase in expression of the epidermal growth factor receptor (EGFR). To determine whether differences in lineage commitment of neural progenitor cells from different stag

Endothelial progenitor cells: diagnostic
โœ Aaron Liew; Frank Barry; Timothy O'Brien ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 303 KB

Endothelial progenitor cells (EPCs) may be defined as adherent cells derived from peripheral blood- or bone marrow-derived mononuclear cells demonstrating acLDL uptake and isolectin-binding capacity. The number of circulating EPCs inversely correlates with the number of cardiovascular risk factors a