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High-resolution 3D imaging uncovers organ-specific vascular control of tissue aging
Author(s) -
Junyu Chen,
Unnikrishnan Sivan,
Sin Lih Tan,
Luciana Lippo,
Jessica De Angelis,
Rossella Labella,
Amit Singh,
Alexandros Chatzis,
Stanley Cheuk,
Mino Medhghalchi,
Jesús Gil,
Georg A. Holländer,
Brian D. Marsden,
Richard Williams,
Saravana K. Ramasamy,
Anjali P. Kusumbe
Publication year - 2021
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.abd7819
Subject(s) - fibrosis , pathology , medicine , blood vessel , organ system , high resolution , anatomy , remote sensing , disease , geology
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.

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