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GROWTH AND SURVIVAL SIGNALS CONTROLLING SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT

Glebova, Natalia O., Ginty, David D.·2005·Annual Review of Neuroscience
DOI 10.1146/annurev.neuro.28.061604.135659
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Abstract

The precise coordination of the many events in nervous system development is absolutely critical for the correct establishment of functional circuits. The postganglionic sympathetic neuron has been an amenable model for studying peripheral nervous system formation. Factors that control several developmental events, including multiple stages of axon extension, neuron survival and death, dendritogenesis, synaptogenesis, and establishment of functional diversity, have been identified in this neuron type. This knowledge allows us to integrate the various intricate processes involved in the formation of a functional sympathetic nervous system and thereby create a paradigm for understanding neuronal development in general.

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  • RNA-seq of hippocampal tissues from middle-aged mice treated with TAC for 3 weeks induced a significant increase in expression of genes positively associated with adult hippocampus neurogenesis and brain function, including Eomes, Dlk1, Gdnf, Dcx, Sox1/2, Gdf11, and Fos.

    “Remarkably, TAC treatment induced a significant increase in the expression of genes positively associated with adult hippocampus neurogenesis and brain function,30–35 including Eomes, a driver of immune cell development & neurogenesis, Dlk1, a mediator of adult hippocampal neurogenesis and cognition, Gdnf, a neurotrophic factor, Dcx, a marker for new-born neurons, Sox1/2, critical determinants of”

    From TERT activation targets DNA methylation and multiple aging hallmarks (2024) · cites this paper as [32]

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Metadata

Authors
Glebova, N. O., & Ginty, D. D.
Affiliations
Department of Neuroscience, Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA;
Venue
Annual Review of Neuroscience
Publisher
Annual Reviews
Published
2005-07-21
Volume
28
Issue
1
Pages
191-222
ISSN
  • 0147-006X
  • 1545-4126
DOI
10.1146/annurev.neuro.28.061604.135659
Cited by
243
References
7
Language
en

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