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HSPA8/HSC70 in Immune Disorders: A Molecular Rheostat that Adjusts Chaperone-Mediated Autophagy Substrates

Title: HSPA8/HSC70 in Immune Disorders: A Molecular Rheostat that Adjusts Chaperone-Mediated Autophagy Substrates
Authors: Bonam, Srinivasa Reddy; Ruff, Marc; Muller, Sylviane
Contributors: Centre National de la Recherche Scientifique (CNRS); Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); ANR-10-LABX-0034,Medalis,Medalis Drug Discovery Center(2010)
Source: ISSN: 2073-4409 ; Cells ; https://hal.science/hal-02361769 ; Cells, 2019, 8 (8), pp.849. ⟨10.3390/cells8080849⟩.
Publisher Information: CCSD; MDPI
Publication Year: 2019
Subject Terms: [SDV.BIO]Life Sciences [q-bio]/Biotechnology
Description: HSPA8/HSC70 is a molecular chaperone involved in a wide variety of cellular processes. It plays a crucial role in protein quality control, ensuring the correct folding and re-folding of selected proteins, and controlling the elimination of abnormally-folded conformers and of proteins daily produced in excess in our cells. HSPA8 is a crucial molecular regulator of chaperone-mediated autophagy, as a detector of substrates that will be processed by this specialized autophagy pathway. In this review, we shortly summarize its structure and overall functions, dissect its implication in immune disorders, and list the known pharmacological tools that modulate its functions. We also exemplify the interest of targeting HSPA8 to regulate pathological immune dysfunctions
Document Type: article in journal/newspaper
Language: English
Relation: PUBMEDCENTRAL: PMC6721745
DOI: 10.3390/cells8080849
Availability: https://hal.science/hal-02361769; https://hal.science/hal-02361769v1/document; https://hal.science/hal-02361769v1/file/islandora_97159.pdf; https://doi.org/10.3390/cells8080849
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.A9B5005B
Database: BASE