4.3 Article

New approaches for solving old problems in neuronal protein trafficking

期刊

MOLECULAR AND CELLULAR NEUROSCIENCE
卷 91, 期 -, 页码 48-66

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2018.04.004

关键词

Synapse; Plasticity; Membrane trafficking; Dendrite; AMPA receptor; Optogenetics

资金

  1. National Science Foundation [DGE-1553798]
  2. Howard Hughes Medical Institute Gilliam Fellowship
  3. National Institutes of Health [NS092421]
  4. National Institute of Neurological Disorders and Stroke [N5082271]
  5. National Institute on Aging [AG058005]
  6. Pew Charitable Trusts
  7. Boettcher Foundation

向作者/读者索取更多资源

Fundamental cellular properties are determined by the repertoire and abundance of proteins displayed on the cell surface. As such, the trafficking mechanisms for establishing and maintaining the surface proteome must be tightly regulated for cells to respond appropriately to extracellular cues, yet plastic enough to adapt to ever-changing environments. Not only are the identity and abundance of surface proteins critical, but in many cases, their regulated spatial positioning within surface nanodomains can greatly impact their function. In the context of neuronal cell biology, surface levels and positioning of ion channels and neurotransmitter receptors play essential roles in establishing important properties, including cellular excitability and synaptic strength. Here we review our current understanding of the trafficking pathways that control the abundance and localization of proteins important for synaptic function and plasticity, as well as recent technological advances that are allowing the field to investigate protein trafficking with increasing spatiotemporal precision.

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