Decreased blood vessel density and endothelial cell subset dynamics during ageing of the endocrine system.
Junyu ChenLuciana LippoRossella LabellaSin Lih TanBrian D MarsdenMichael L DustinSaravana K RamasamyAnjali P KusumbePublished in: The EMBO journal (2020)
Age-associated alterations of the hormone-secreting endocrine system cause organ dysfunction and disease states. However, the cell biology of endocrine tissue ageing remains poorly understood. Here, we perform comparative 3D imaging to understand age-related perturbations of the endothelial cell (EC) compartment in endocrine glands. Datasets of a wide range of markers highlight a decline in capillary and artery numbers, but not of perivascular cells in pancreas, testis and thyroid gland, with age in mice and humans. Further, angiogenesis and β-cell expansion in the pancreas are coupled by a distinct age-dependent subset of ECs. While this EC subpopulation supports pancreatic β cells, it declines during ageing concomitant with increased expression of the gap junction protein Gja1. EC-specific ablation of Gja1 restores β-cell expansion in the aged pancreas. These results provide a proof of concept for understanding age-related vascular changes and imply that therapeutic targeting of blood vessels may restore aged endocrine tissue function. This comprehensive data atlas offers over > 1,000 multicolour volumes for exploration and research in endocrinology, ageing, matrix and vascular biology.
Keyphrases
- single cell
- endothelial cells
- induced apoptosis
- cell therapy
- cell cycle arrest
- rna seq
- oxidative stress
- high resolution
- poor prognosis
- type diabetes
- cell death
- endoplasmic reticulum stress
- mass spectrometry
- stem cells
- signaling pathway
- machine learning
- mesenchymal stem cells
- electronic health record
- adipose tissue
- skeletal muscle
- insulin resistance
- cell proliferation
- bone marrow
- vascular endothelial growth factor
- pi k akt
- high glucose