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Autophagy in Plasma Cell Ontogeny and Malignancy

Autophagy is a highly conserved pathway that recycles cytosolic material and organelles via lysosomal degradation. Once simplistically viewed as a non-selective survival strategy in dire straits, autophagy has emerged as a tightly regulated process ensuring organelle function, proteome plasticity, c...

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Detalles Bibliográficos
Autores principales: Milan, Enrico, Fabbri, Monica, Cenci, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891390/
https://www.ncbi.nlm.nih.gov/pubmed/26984755
http://dx.doi.org/10.1007/s10875-016-0254-9
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author Milan, Enrico
Fabbri, Monica
Cenci, Simone
author_facet Milan, Enrico
Fabbri, Monica
Cenci, Simone
author_sort Milan, Enrico
collection PubMed
description Autophagy is a highly conserved pathway that recycles cytosolic material and organelles via lysosomal degradation. Once simplistically viewed as a non-selective survival strategy in dire straits, autophagy has emerged as a tightly regulated process ensuring organelle function, proteome plasticity, cell differentiation and tissue homeostasis, with key roles in physiology and disease. Selective target recognition, mediated by specific adapter proteins, enables autophagy to orchestrate highly specialized functions in innate and adaptive immunity. Among them, the shaping of plasma cells for sustainable antibody production through a negative control on their differentiation program. Moreover, memory B cells and long-lived plasma cells require autophagy to exist. Further, the plasma cell malignancy, multiple myeloma deploys abundant autophagy, essential for homeostasis, survival and drug resistance.
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spelling pubmed-48913902016-06-17 Autophagy in Plasma Cell Ontogeny and Malignancy Milan, Enrico Fabbri, Monica Cenci, Simone J Clin Immunol Article Autophagy is a highly conserved pathway that recycles cytosolic material and organelles via lysosomal degradation. Once simplistically viewed as a non-selective survival strategy in dire straits, autophagy has emerged as a tightly regulated process ensuring organelle function, proteome plasticity, cell differentiation and tissue homeostasis, with key roles in physiology and disease. Selective target recognition, mediated by specific adapter proteins, enables autophagy to orchestrate highly specialized functions in innate and adaptive immunity. Among them, the shaping of plasma cells for sustainable antibody production through a negative control on their differentiation program. Moreover, memory B cells and long-lived plasma cells require autophagy to exist. Further, the plasma cell malignancy, multiple myeloma deploys abundant autophagy, essential for homeostasis, survival and drug resistance. Springer US 2016-03-16 2016 /pmc/articles/PMC4891390/ /pubmed/26984755 http://dx.doi.org/10.1007/s10875-016-0254-9 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Milan, Enrico
Fabbri, Monica
Cenci, Simone
Autophagy in Plasma Cell Ontogeny and Malignancy
title Autophagy in Plasma Cell Ontogeny and Malignancy
title_full Autophagy in Plasma Cell Ontogeny and Malignancy
title_fullStr Autophagy in Plasma Cell Ontogeny and Malignancy
title_full_unstemmed Autophagy in Plasma Cell Ontogeny and Malignancy
title_short Autophagy in Plasma Cell Ontogeny and Malignancy
title_sort autophagy in plasma cell ontogeny and malignancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891390/
https://www.ncbi.nlm.nih.gov/pubmed/26984755
http://dx.doi.org/10.1007/s10875-016-0254-9
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