Long-distance regressive signaling in neural development and disease.


Journal

Wiley interdisciplinary reviews. Developmental biology
ISSN: 1759-7692
Titre abrégé: Wiley Interdiscip Rev Dev Biol
Pays: United States
ID NLM: 101576624

Informations de publication

Date de publication:
03 2021
Historique:
received: 02 10 2019
revised: 23 03 2020
accepted: 06 04 2020
pubmed: 12 5 2020
medline: 25 12 2021
entrez: 12 5 2020
Statut: ppublish

Résumé

Nervous system development proceeds via well-orchestrated processes involving a balance between progressive and regressive events including stabilization or elimination of axons, synapses, and even entire neurons. These progressive and regressive events are driven by functionally antagonistic signaling pathways with the dominant pathway eventually determining whether a neural element is retained or removed. Many of these developmental sculpting events are triggered by final target innervation necessitating a long-distance mode of communication. While long-distance progressive signaling has been well characterized, particularly for neurotrophic factors, there remains relatively little known about how regressive events are triggered from a distance. Here we discuss the emergent phenomenon of long-distance regressive signaling pathways. In particular, we will cover (a) progressive and regressive cues known to be employed after target innervation, (b) the mechanisms of long-distance signaling from an endosomal platform, (c) recent evidence that long-distance regressive cues emanate from platforms like death receptors or repulsive axon guidance receptors, and (d) evidence that these pathways are exploited in pathological scenarios. This article is categorized under: Nervous System Development > Vertebrates: General Principles Signaling Pathways > Global Signaling Mechanisms Establishment of Spatial and Temporal Patterns > Cytoplasmic Localization.

Identifiants

pubmed: 32391977
doi: 10.1002/wdev.382
pmc: PMC7655682
mid: NIHMS1640413
doi:

Substances chimiques

Nerve Growth Factors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e382

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS102365
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD103537
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS091617
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS107456
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008715
Pays : United States

Informations de copyright

© 2020 Wiley Periodicals LLC.

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Auteurs

Amrita Pathak (A)

Department of Biochemistry and Vanderbilt Brain Institute, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Shayla Clark (S)

Neuroscience Graduate Program, University of Virginia, Charlottesville, Virginia, USA.

Francisca C Bronfman (FC)

Institute of Biomedical Sciences (ICB), Faculty of Medicine, Faculty of Life Science, Universidad Andres Bello, Santiago, Chile.

Christopher D Deppmann (CD)

Departments of Biology, Cell Biology, Biomedical Engineering, and Neuroscience, University of Virginia, Charlottesville, Virginia, USA.

Bruce D Carter (BD)

Department of Biochemistry and Vanderbilt Brain Institute, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

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