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High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging
Blood vessels provide supportive microenvironments for maintaining tissue functions. Age-associated vascular changes and their relation to tissue aging and pathology are poorly understood. Here, we perform 3D imaging of young and aging vascular beds. Multiple organs in mice and humans demonstrate an...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857692/ https://www.ncbi.nlm.nih.gov/pubmed/33536212 http://dx.doi.org/10.1126/sciadv.abd7819 |
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author | Chen, Junyu Sivan, Unnikrishnan Tan, Sin Lih Lippo, Luciana De Angelis, Jessica Labella, Rossella Singh, Amit Chatzis, Alexandros Cheuk, Stanley Medhghalchi, Mino Gil, Jesus Hollander, Georg Marsden, Brian D. Williams, Richard Ramasamy, Saravana K. Kusumbe, Anjali P. |
author_facet | Chen, Junyu Sivan, Unnikrishnan Tan, Sin Lih Lippo, Luciana De Angelis, Jessica Labella, Rossella Singh, Amit Chatzis, Alexandros Cheuk, Stanley Medhghalchi, Mino Gil, Jesus Hollander, Georg Marsden, Brian D. Williams, Richard Ramasamy, Saravana K. Kusumbe, Anjali P. |
author_sort | Chen, Junyu |
collection | PubMed |
description | Blood vessels provide supportive microenvironments for maintaining tissue functions. Age-associated vascular changes and their relation to tissue aging and pathology are poorly understood. Here, we perform 3D imaging of young and aging vascular beds. Multiple organs in mice and humans demonstrate an age-dependent decline in vessel density and pericyte numbers, while highly remodeling tissues such as skin preserve the vasculature. Vascular attrition precedes the appearance of cellular hallmarks of aging such as senescence. Endothelial VEGFR2 loss-of-function mice demonstrate that vascular perturbations are sufficient to stimulate cellular changes coupled with aging. Age-associated tissue-specific molecular changes in the endothelium drive vascular loss and dictate pericyte to fibroblast differentiation. Lineage tracing of perivascular cells with inducible PDGFRβ and NG2 Cre mouse lines demonstrated that increased pericyte to fibroblast differentiation distinguishes injury-induced organ fibrosis and zymosan-induced arthritis. To spur further discoveries, we provide a freely available resource with 3D vascular and tissue maps. |
format | Online Article Text |
id | pubmed-7857692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78576922021-02-16 High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging Chen, Junyu Sivan, Unnikrishnan Tan, Sin Lih Lippo, Luciana De Angelis, Jessica Labella, Rossella Singh, Amit Chatzis, Alexandros Cheuk, Stanley Medhghalchi, Mino Gil, Jesus Hollander, Georg Marsden, Brian D. Williams, Richard Ramasamy, Saravana K. Kusumbe, Anjali P. Sci Adv Research Articles Blood vessels provide supportive microenvironments for maintaining tissue functions. Age-associated vascular changes and their relation to tissue aging and pathology are poorly understood. Here, we perform 3D imaging of young and aging vascular beds. Multiple organs in mice and humans demonstrate an age-dependent decline in vessel density and pericyte numbers, while highly remodeling tissues such as skin preserve the vasculature. Vascular attrition precedes the appearance of cellular hallmarks of aging such as senescence. Endothelial VEGFR2 loss-of-function mice demonstrate that vascular perturbations are sufficient to stimulate cellular changes coupled with aging. Age-associated tissue-specific molecular changes in the endothelium drive vascular loss and dictate pericyte to fibroblast differentiation. Lineage tracing of perivascular cells with inducible PDGFRβ and NG2 Cre mouse lines demonstrated that increased pericyte to fibroblast differentiation distinguishes injury-induced organ fibrosis and zymosan-induced arthritis. To spur further discoveries, we provide a freely available resource with 3D vascular and tissue maps. American Association for the Advancement of Science 2021-02-03 /pmc/articles/PMC7857692/ /pubmed/33536212 http://dx.doi.org/10.1126/sciadv.abd7819 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Chen, Junyu Sivan, Unnikrishnan Tan, Sin Lih Lippo, Luciana De Angelis, Jessica Labella, Rossella Singh, Amit Chatzis, Alexandros Cheuk, Stanley Medhghalchi, Mino Gil, Jesus Hollander, Georg Marsden, Brian D. Williams, Richard Ramasamy, Saravana K. Kusumbe, Anjali P. High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title | High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title_full | High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title_fullStr | High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title_full_unstemmed | High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title_short | High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging |
title_sort | high-resolution 3d imaging uncovers organ-specific vascular control of tissue aging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857692/ https://www.ncbi.nlm.nih.gov/pubmed/33536212 http://dx.doi.org/10.1126/sciadv.abd7819 |
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