| Literature DB >> 34309183 |
Jörg Höhfeld1, Thomas Benzing2, Wilhelm Bloch3, Dieter O Fürst1, Sebastian Gehlert3,4, Michael Hesse5, Bernd Hoffmann6, Thorsten Hoppe7, Pitter F Huesgen8,9, Maja Köhn10, Waldemar Kolanus11, Rudolf Merkel6, Carien M Niessen12, Wojciech Pokrzywa13, Markus M Rinschen14,15, Dagmar Wachten16, Bettina Warscheid17.
Abstract
Cell survival, tissue integrity and organismal health depend on the ability to maintain functional protein networks even under conditions that threaten protein integrity. Protection against such stress conditions involves the adaptation of folding and degradation machineries, which help to preserve the protein network by facilitating the refolding or disposal of damaged proteins. In multicellular organisms, cells are permanently exposed to stress resulting from mechanical forces. Yet, for long time mechanical stress was not recognized as a primary stressor that perturbs protein structure and threatens proteome integrity. The identification and characterization of protein folding and degradation systems, which handle force-unfolded proteins, marks a turning point in this regard. It has become apparent that mechanical stress protection operates during cell differentiation, adhesion and migration and is essential for maintaining tissues such as skeletal muscle, heart and kidney as well as the immune system. Here, we provide an overview of recent advances in our understanding of mechanical stress protection.Entities:
Keywords: autophagy; chaperones; mechanobiology; proteostasis; signal transduction
Year: 2021 PMID: 34309183 DOI: 10.15252/embr.202152507
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807