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Open AccessJournal ArticleDOI

Shaping proteostasis at the cellular, tissue, and organismal level.

Ambre Sala, +2 more
- 01 May 2017 - 
- Vol. 216, Iss: 5, pp 1231-1241
TLDR
This review by Morimoto and colleagues examines mechanisms by which protein homeostasis (proteostasis) is achieved in multicellular organisms and discusses the implications for health and disease.
Abstract
The proteostasis network (PN) regulates protein synthesis, folding, transport, and degradation to maintain proteome integrity and limit the accumulation of protein aggregates, a hallmark of aging and degenerative diseases. In multicellular organisms, the PN is regulated at the cellular, tissue, and systemic level to ensure organismal health and longevity. Here we review these three layers of PN regulation and examine how they collectively maintain cellular homeostasis, achieve cell type-specific proteomes, and coordinate proteostasis across tissues. A precise understanding of these layers of control has important implications for organismal health and could offer new therapeutic approaches for neurodegenerative diseases and other chronic disorders related to PN dysfunction.

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Citations
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Journal ArticleDOI

The proteostasis network and its decline in ageing.

TL;DR: The possibilities of pharmacological augmentation of the capacity of proteostasis networks hold great promise for delaying the onset of age-related pathologies associated with proteome deterioration and for extending healthspan.
Journal ArticleDOI

Pathways of cellular proteostasis in aging and disease.

TL;DR: Klaips et al. outline the pathways and molecular mechanisms of cellular protein homeostasis, or protestasis, and discuss how a decline in proteostasis during aging contributes to disease.
Journal ArticleDOI

Aging, inflammation and the environment

TL;DR: It is pointed out that longitudinal studies with a life course approach are needed to gain further mechanistic insight on the processes that lead to functional decline with aging, and the role played by inflammation and environmental challenges.
Journal ArticleDOI

Alzheimer’s Disease: From Firing Instability to Homeostasis Network Collapse

TL;DR: It is hypothesized that firing instability and impaired synaptic plasticity at early AD stages trigger a vicious cycle, leading to dysregulation of the whole IHN, and represents the major driving force of the transition from early memory impairments to neurodegeneration.
Journal ArticleDOI

Functional Modules of the Proteostasis Network

TL;DR: The capacity and limitations of the PN in maintaining proteome integrity in the face of proteotoxic stresses, such as aggregate formation in neurodegenerative diseases are discussed.
References
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Journal ArticleDOI

Neuronal GPCR Controls Innate Immunity by Regulating Noncanonical Unfolded Protein Response Genes

TL;DR: OCTR-1, a putative octopamine G protein–coupled catecholamine receptor, functioned in sensory neurons designated ASH and ASI to actively suppress innate immune responses by down-regulating the expression of noncanonical UPR genes pqn/abu in nonneuronal tissues.
Journal ArticleDOI

Differential Scales of Protein Quality Control

TL;DR: These layered defenses help protect cells from damaged proteins and use compartmentalized defenses and networks of communication, capable sometimes of signaling between cells, to respond to changes in the proteome's health.
Journal ArticleDOI

Genome-wide screen for modifiers of ataxin-3 neurodegeneration in Drosophila.

TL;DR: Findings provide new insight into molecular pathways of polyQ toxicity, defining novel targets for promoting neuronal survival in human neurodegenerative disease.
Journal ArticleDOI

Small-molecule proteostasis regulators for protein conformational diseases

TL;DR: It is suggested that modulation of the proteostasis network by PRs represents a promising therapeutic approach for the treatment of a variety of protein conformational diseases.
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