| Literature DB >> 33536212 |
Junyu Chen1,2, Unnikrishnan Sivan1, Sin Lih Tan1, Luciana Lippo1, Jessica De Angelis1, Rossella Labella1, Amit Singh1,3, Alexandros Chatzis1, Stanley Cheuk4,5, Mino Medhghalchi6, Jesus Gil7,8, Georg Hollander4, Brian D Marsden6,9, Richard Williams6, Saravana K Ramasamy7,8, Anjali P Kusumbe10.
Abstract
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.Entities:
Year: 2021 PMID: 33536212 PMCID: PMC7857692 DOI: 10.1126/sciadv.abd7819
Source DB: PubMed Journal: Sci Adv ISSN: 2375-2548 Impact factor: 14.136