scispace - formally typeset
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.

read more

Content maybe subject to copyright    Report

Citations
More filters
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
More filters
Journal ArticleDOI

Organismal proteostasis: role of cell-nonautonomous regulation and transcellular chaperone signaling

TL;DR: It is proposed that transcellular chaperone signaling provides a critical control step for the PN to maintain cellular and organismal health span when challenged by acute stress and upon chronic expression of metastable proteins.
Journal ArticleDOI

Heat shock factor functions at the convergence of the stress response and developmental pathways in Caenorhabditis elegans.

TL;DR: It is demonstrated that HSF is required for normal postembryonic development under physiological conditions and a dramatic reversal of dauer formation was observed, indicating thatHSF is also required in the dauer pathway.
Journal ArticleDOI

Protein quality control gets muscle into shape.

TL;DR: The interplay between chaperone activity and protein degradation in respect to the formation and maintenance of muscle during physiological and pathological conditions is highlighted.
Journal ArticleDOI

The Mitochondria-Regulated Immune Pathway Activated in the C. elegans Intestine Is Neuroprotective

TL;DR: It is shown that the p38MAPK-mediated immune pathway activated in intestinal cells of Caenorhabditis elegans upon mitochondrial dysfunction protects neurons in a cell-non-autonomous fashion, and proposed that mitochondria are subject to constant surveillance by innate immune mechanisms.
Journal ArticleDOI

A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy

TL;DR: It is shown that ASC-JM17 ameliorates toxicity of the mutant androgen receptor (AR) responsible for SBMA in cell, fly and mouse models and indicates that activation of the Nrf1/Nrf2 pathway is a viable option for pharmacological intervention in SBMA and potentially other polyglutamine diseases.
Related Papers (5)