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PMID: 12357985 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Mechanisms regulating lineage diversity during mammalian cerebral cortical neurogenesis and gliogenesis.

Results and problems in cell differentiation ·Vol. 39 ·2002-00-00 ·Pages 27-52

Mehler MF

Abstract

During mammalian cerebral cortical development, neural stem cells (NSCs) present within periventricular generative zones give rise to successive waves of neurons and radial glia, followed by oligodendrocytes and astrocytes. The molecular and cellular mechanisms that orchestrate these precisely timed and progressive maturational events are still largely undefined. These developmental processes are likely to involve the dynamic interplay of environmental signals, cell-cell interactions and transcriptional regulatory events. The bone morphogenetic proteins (BMPs), an expanding subclass of the transforming growth factor beta cytokine superfamily, may represent an important set of environmental cues for these progressive maturational events because of the broad profiles of developmental expression of the requisite BMP ligands, receptor subunits and intracellular transduction elements, and because of their versatile roles in promoting a spectrum of cellular processes intimately involved in progressive neural fate decisions. The BMPs also interact with complementary regional environmental signals such as the basic fibroblast growth factor (bFGF) and sonic hedgehog (Shh) that promote earlier stages of NSC expansion, self-renewal, lineage restriction and incipient lineage commitment. The ability of these cytokines and trophic signals to act within specific neurodevelopmental contexts may, in turn, depend on the composite actions of cell-cell contact-associated signals, such as Notch-Hes-mediated lateral inhibitory pathways, and additional transcriptional modulatory events, such as those mediated by members of the inhibitor of differentiation (ID) gene family that encode a novel set of negative basic helix-loop-helix (bHLH) transcription factors. In this chapter, we will examine the distinct roles of these different classes of developmental cues in defining the biological properties of an integrated cerebral cortical developmental signaling network. Ongoing studies in this exciting area of mammalian central nervous system (CNS) development will help to identify important molecular and cellular targets for evolving pharmacological, gene and stem cell therapeutic interventions to combat the pathological sequelae of a spectrum of acquired and genetic disorders of the central nervous system.

MeSH Terms
Animals Astrocytes/cytology Bone Morphogenetic Proteins/physiology Cell Differentiation Cell Lineage Cerebral Cortex/embryology Fibroblast Growth Factor 2/physiology Forecasting Hedgehog Proteins Mammals Models, Neurological Neuroglia/physiology Neurons/cytology Oligodendroglia/cytology Signal Transduction Stem Cells/cytology Trans-Activators/physiology Transcription Factors/genetics,physiology
Chemicals
Bone Morphogenetic Proteins Hedgehog Proteins Trans-Activators Transcription Factors Fibroblast Growth Factor 2
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Mehler Mark F
Departments of Neurology, Neuroscience and Psychiatry, Rose F. Kennedy Center for Research in Mental Retardation and Developmental Disabilities, Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Article Info
Journal
Results and problems in cell differentiation
Abbr.
Results Probl Cell Differ
ISSN
0080-1844
Published
2002-00-00
Pages
27-52
Language
English
Region
Germany
NLM ID
0173555
Subset
IM
Grants
NIMH NIH HHS · R01 MH066290 · United States
NINDS NIH HHS · R01 NS038902 · United States
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