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5. Mammalian adipogenesis regulators (Aregs) exhibit robust non - bioRxiv
24 feb 2021 · Abstract. Adipose stem and precursor cells (ASPCs) give rise to adipocytes and determine the composition and plasticity of adipose tissue.
Adipose stem and precursor cells (ASPCs) give rise to adipocytes and determine the composition and plasticity of adipose tissue. Recently, several studies have demonstrated that ASPCs partition into at least three distinct cell subpopulations: Dpp4 + stem-like cells, Aoc 3+ pre-adipocyte-like cells, and the enigmatic CD142+ cells. A great challenge now is to functionally characterize these distinct ASPC populations. Here, we focus on CD142+ ASPCs since discrepant properties have been assigned to this subpopulation, from adipogenic to non- and even anti-adipogenic. To address these inconsistencies, we comprehensively characterized mammalian subcutaneous CD142+ ASPCs across various sampling conditions. Our findings demonstrate that CD142+ ASPCs exhibit high molecular and phenotypic robustness, firmly supporting their non- and anti-adipogenic properties. However, these properties emerge in an age-dependent manner, revealing surprising temporal CD142+ ASPC behavioural alterations. Finally, using multi-omic and functional assays, we show that the inhibitory nature of these adipogenesis-regulatory CD142+ ASPCs (Aregs) is driven by specifically expressed secretory factors that cooperate with the retinoic acid signalling pathway to transform the adipogenic state of CD142− ASPCs into a non-adipogenic, Areg-like one. ### Competing Interest Statement The authors have declared no competing interest.
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8. Mammalian adipogenesis regulator (Areg) cells use retinoic acid ... - NCBI
Finally, using multi‐omic and functional assays, we show that the inhibitory nature of these adipogenesis‐regulatory CD142+ ASPCs (Aregs) is driven by ...
Adipose stem and precursor cells (ASPCs) give rise to adipocytes and determine the composition and plasticity of adipose tissue. Recently, several studies have demonstrated that ASPCs partition into at least three distinct cell subpopulations, including ...
9. A single-cell-based identification and characterisation of Aregs, an ...
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Adipose tissue is an essential element in energy conservation mechanisms. Its unique plasticity is driven by the ability of adipocytes to accumulate and liberate lipids as a function of the energetic status of the organism. Given the recent rise in the global incidence of obesity, there is great interest in understanding the mechanisms behind disturbed energy balance. However, the heterogeneity of adipose tissue and of the somatic stem cells giving rise to mature adipocytes, makes it extremely challenging to characterise the cellular and molecular identity of fat depots. Single-cell RNA sequencing has recently enabled ground-breaking insights into the composition of complex cell populations. Our single cell-based dissection of adipogenic precursors revealed the existence of distinct cell sub-populations within the murine subcutaneous fat depot. We demonstrated that one of these populations, characterised by a high expression of F3 gene (encoding CD142), showed a completely non-adipogenic phenotype. Moreover, it revealed to be regulatory towards other adipose stem and precursor cells by supressing their ability to form adipocytes in a paracrine manner. These adipogenic regulatory cells, which we termed Aregs, proved to maintain their inhibitory properties in vivo and were shown phenotypically conserved in humans. We next established the robustness of Aregs as a novel cell sub-type in the context of various isolation strategies, the strength of the adipogenic cue and sex-based...
