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Single-nucleus transcriptome analysis identifies a novel FKBP5+ endothelial cell subtype involved in endothelial-to-mesenchymal transition in adipose tissue during aging.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Aug 30; Vol. 722, pp. 150157. Date of Electronic Publication: 2024 May 22. - Publication Year :
- 2024
-
Abstract
- Age-associated adipose tissue (AT) dysfunction is multifactorial and often leads to detrimental health consequences. AT is highly vascularized and endothelial cells (ECs) has been recently identified as a key regulator in the homeostasis of AT. However, the alteration of cell composition in AT during aging and the communication between endothelial cells and adipocytes remain poorly understood. In this study, we take advantage of single nucleus RNA sequencing analysis, and discovered a group of FKBP5+ ECs specifically resident in aged AT. Of interest, FKBP5+ ECs exhibited the potential for endothelial-to-mesenchymal transition (EndoMT) and exhibited a critical role in regulating adipocytes. Furthermore, lineage tracing experiments demonstrated that ECs in aged AT tend to express FKBP5 and undergo EndoMT with progressive loss of endothelial marker. This study may provide a basis for a new mechanism of microvascular ECs-induced AT dysfunction during aging.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024. Published by Elsevier Inc.)
- Subjects :
- Animals
Male
Mice
Adipocytes metabolism
Adipocytes cytology
Cell Nucleus metabolism
Epithelial-Mesenchymal Transition genetics
Gene Expression Profiling
Mice, Inbred C57BL
Single-Cell Analysis methods
Tacrolimus Binding Proteins metabolism
Tacrolimus Binding Proteins genetics
Transcriptome
Adipose Tissue metabolism
Adipose Tissue cytology
Aging metabolism
Aging genetics
Endothelial Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 722
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 38805789
- Full Text :
- https://doi.org/10.1016/j.bbrc.2024.150157