Cargando…

Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies

Chaperone-mediated autophagy (CMA) ensures the selective degradation of cellular proteins endowed with a KFERQ-like motif by lysosomes. It is estimated that 30% of all cellular proteins can be directed to the lysosome for CMA degradation, but only a few substrates have been formally identified so fa...

Descripción completa

Detalles Bibliográficos
Autores principales: Robert, Guillaume, Jacquel, Arnaud, Auberger, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830112/
https://www.ncbi.nlm.nih.gov/pubmed/31623164
http://dx.doi.org/10.3390/cells8101260
_version_ 1783465712199663616
author Robert, Guillaume
Jacquel, Arnaud
Auberger, Patrick
author_facet Robert, Guillaume
Jacquel, Arnaud
Auberger, Patrick
author_sort Robert, Guillaume
collection PubMed
description Chaperone-mediated autophagy (CMA) ensures the selective degradation of cellular proteins endowed with a KFERQ-like motif by lysosomes. It is estimated that 30% of all cellular proteins can be directed to the lysosome for CMA degradation, but only a few substrates have been formally identified so far. Mechanistically, the KFERQ-like motifs present in substrate proteins are recognized by the molecular chaperone Hsc70c (Heat shock cognate 71 kDa protein cytosolic), also known as HSPA8, and directed to LAMP2A, which acts as the CMA receptor at the lysosomal surface. Following linearization, the protein substrate is next transported to the lumen of the lysosomes, where it is degraded by resident proteases, mainly cathepsins and eventually recycled to sustain cellular homeostasis. CMA is induced by different stress conditions, including energy deprivation that also activates macro-autophagy (MA), that may make it difficult to decipher the relative impact of both pathways on cellular homeostasis. Besides common inducing triggers, CMA and MA might be induced as compensatory mechanisms when either mechanism is altered, as it is the often the case in different pathological settings. Therefore, CMA activation can compensate for alterations of MA and vice versa. In this context, these compensatory mechanisms, when occurring, may be targeted for therapeutic purposes. Both processes have received particular attention from scientists and clinicians, since modulation of MA and CMA may have a profound impact on cellular proteostasis, metabolism, death, differentiation, and survival and, as such, could be targeted for therapeutic intervention in degenerative and immune diseases, as well as in cancer, including hematopoietic malignancies. The role of MA in cancer initiation and progression is now well established, but whether and how CMA is involved in tumorigenesis has been only sparsely explored. In the present review, we encompass the description of the mechanisms involved in CMA, its function in the physiology and pathogenesis of hematopoietic cells, its emerging role in cancer initiation and development, and, finally, the potential therapeutic opportunity to target CMA or CMA-mediated compensatory mechanisms in hematological malignancies.
format Online
Article
Text
id pubmed-6830112
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-68301122019-11-20 Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies Robert, Guillaume Jacquel, Arnaud Auberger, Patrick Cells Review Chaperone-mediated autophagy (CMA) ensures the selective degradation of cellular proteins endowed with a KFERQ-like motif by lysosomes. It is estimated that 30% of all cellular proteins can be directed to the lysosome for CMA degradation, but only a few substrates have been formally identified so far. Mechanistically, the KFERQ-like motifs present in substrate proteins are recognized by the molecular chaperone Hsc70c (Heat shock cognate 71 kDa protein cytosolic), also known as HSPA8, and directed to LAMP2A, which acts as the CMA receptor at the lysosomal surface. Following linearization, the protein substrate is next transported to the lumen of the lysosomes, where it is degraded by resident proteases, mainly cathepsins and eventually recycled to sustain cellular homeostasis. CMA is induced by different stress conditions, including energy deprivation that also activates macro-autophagy (MA), that may make it difficult to decipher the relative impact of both pathways on cellular homeostasis. Besides common inducing triggers, CMA and MA might be induced as compensatory mechanisms when either mechanism is altered, as it is the often the case in different pathological settings. Therefore, CMA activation can compensate for alterations of MA and vice versa. In this context, these compensatory mechanisms, when occurring, may be targeted for therapeutic purposes. Both processes have received particular attention from scientists and clinicians, since modulation of MA and CMA may have a profound impact on cellular proteostasis, metabolism, death, differentiation, and survival and, as such, could be targeted for therapeutic intervention in degenerative and immune diseases, as well as in cancer, including hematopoietic malignancies. The role of MA in cancer initiation and progression is now well established, but whether and how CMA is involved in tumorigenesis has been only sparsely explored. In the present review, we encompass the description of the mechanisms involved in CMA, its function in the physiology and pathogenesis of hematopoietic cells, its emerging role in cancer initiation and development, and, finally, the potential therapeutic opportunity to target CMA or CMA-mediated compensatory mechanisms in hematological malignancies. MDPI 2019-10-16 /pmc/articles/PMC6830112/ /pubmed/31623164 http://dx.doi.org/10.3390/cells8101260 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Robert, Guillaume
Jacquel, Arnaud
Auberger, Patrick
Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title_full Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title_fullStr Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title_full_unstemmed Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title_short Chaperone-Mediated Autophagy and Its Emerging Role in Hematological Malignancies
title_sort chaperone-mediated autophagy and its emerging role in hematological malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830112/
https://www.ncbi.nlm.nih.gov/pubmed/31623164
http://dx.doi.org/10.3390/cells8101260
work_keys_str_mv AT robertguillaume chaperonemediatedautophagyanditsemergingroleinhematologicalmalignancies
AT jacquelarnaud chaperonemediatedautophagyanditsemergingroleinhematologicalmalignancies
AT aubergerpatrick chaperonemediatedautophagyanditsemergingroleinhematologicalmalignancies