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Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency
In different organs and tissues, the lymphatic system serves as a drainage system for interstitial fluid and is useful for removing substances that would otherwise accumulate in the interstitium. In the brain, which lacks lymphatic circulation, the drainage and cleaning function is performed by the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860256/ https://www.ncbi.nlm.nih.gov/pubmed/36409907 http://dx.doi.org/10.1073/pnas.2211326119 |
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author | Riba, Marta del Valle, Jaume Molina-Porcel, Laura Pelegrí, Carme Vilaplana, Jordi |
author_facet | Riba, Marta del Valle, Jaume Molina-Porcel, Laura Pelegrí, Carme Vilaplana, Jordi |
author_sort | Riba, Marta |
collection | PubMed |
description | In different organs and tissues, the lymphatic system serves as a drainage system for interstitial fluid and is useful for removing substances that would otherwise accumulate in the interstitium. In the brain, which lacks lymphatic circulation, the drainage and cleaning function is performed by the glymphatic system, called so for its dependence on glial cells and its similar function to that of the lymphatic system. In the present article, we define glymphatic insufficiency as the inability of the glymphatic system to properly perform the brain cleaning function. Furthermore, we propose that corpora amylacea or wasteosomes, which are protective structures that act as waste containers and accumulate waste products, are, in fact, a manifestation of chronic glymphatic insufficiency. Assuming this premise, we provide an explanation that coherently links the formation, distribution, structure, and function of these bodies in the human brain. Moreover, we open up new perspectives in the study of the glymphatic system since wasteosomes can provide information about which variables have the greatest impact on the glymphatic system and which diseases occur with chronic glymphatic insufficiency. For example, based on the presence of wasteosomes, it seems that aging, sleep disorders, and cerebrovascular pathologies have the highest impact on the glymphatic system, whereas neurodegenerative diseases have a more limited impact. Furthermore, as glymphatic insufficiency is a risk factor for neurodegenerative diseases, information provided by wasteosomes could help to define the strategies and actions that can prevent glymphatic disruptions, thus limiting the risk of developing neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-9860256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-98602562023-02-01 Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency Riba, Marta del Valle, Jaume Molina-Porcel, Laura Pelegrí, Carme Vilaplana, Jordi Proc Natl Acad Sci U S A Perspective In different organs and tissues, the lymphatic system serves as a drainage system for interstitial fluid and is useful for removing substances that would otherwise accumulate in the interstitium. In the brain, which lacks lymphatic circulation, the drainage and cleaning function is performed by the glymphatic system, called so for its dependence on glial cells and its similar function to that of the lymphatic system. In the present article, we define glymphatic insufficiency as the inability of the glymphatic system to properly perform the brain cleaning function. Furthermore, we propose that corpora amylacea or wasteosomes, which are protective structures that act as waste containers and accumulate waste products, are, in fact, a manifestation of chronic glymphatic insufficiency. Assuming this premise, we provide an explanation that coherently links the formation, distribution, structure, and function of these bodies in the human brain. Moreover, we open up new perspectives in the study of the glymphatic system since wasteosomes can provide information about which variables have the greatest impact on the glymphatic system and which diseases occur with chronic glymphatic insufficiency. For example, based on the presence of wasteosomes, it seems that aging, sleep disorders, and cerebrovascular pathologies have the highest impact on the glymphatic system, whereas neurodegenerative diseases have a more limited impact. Furthermore, as glymphatic insufficiency is a risk factor for neurodegenerative diseases, information provided by wasteosomes could help to define the strategies and actions that can prevent glymphatic disruptions, thus limiting the risk of developing neurodegenerative diseases. National Academy of Sciences 2022-11-21 2022-11-29 /pmc/articles/PMC9860256/ /pubmed/36409907 http://dx.doi.org/10.1073/pnas.2211326119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Perspective Riba, Marta del Valle, Jaume Molina-Porcel, Laura Pelegrí, Carme Vilaplana, Jordi Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title | Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title_full | Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title_fullStr | Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title_full_unstemmed | Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title_short | Wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
title_sort | wasteosomes (corpora amylacea) as a hallmark of chronic glymphatic insufficiency |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860256/ https://www.ncbi.nlm.nih.gov/pubmed/36409907 http://dx.doi.org/10.1073/pnas.2211326119 |
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