Work

Adiponectin receptor T-cadherin emerges as a novel regulator of adipose stem cell quiescence and adipogenesis

Year: 2026

Type: article

Abstract: The question of heterogeneity among adipose tissue cells and mesenchymal stem/stromal cells mesenchymal stem cells derived from white adipose tissue has long been a subject of interest. In our study, we conducted a comprehensive single-cell RNA-seq analysis on MSCs isolated from human subcutaneous adipose tissue and maintained under control conditions or upon adipogenic induction. Our findings unveiled a distinct subpopulation of T-cadherin expressing cells, which co-expressed Dipeptidyl peptidase–4 (DPP4 + ), a marker of multipotent progenitors in the adipose tissue. Moreover, T-cadherin co-expressed with DPP4 + in early progenitors both, in vivo and in vitro . While adipogenic induction resulted in overall T-cadherin decline, in both the control and differentiated samples, there existed cells with high T-cadherin concurrently expressing stemness-related genes. Pseudotemporal trajectories analysis based on the scRNA-seq data, revealed that T-cadherin-expressing cells constituted a discrete cell subpopulation with stem-like properties, rather than participating in adipogenic differentiation. Using lentiviral transduction, we manipulated T-cadherin expression in MSCs and found that cells overexpressing T-cadherin also displayed an elevated level of DPP4. Strikingly, these cells exhibited significantly slower rates of proliferation compared to the controls. Long-term live-cell imaging, which allowed for the tracking of individual cell fates over a span of 10 days, together with classical adipogenic differentiation assays, revealed a substantial reduction in adipogenic differentiation capacity among MSCs overexpressing T-cadherin. Consequently, our experimental findings support a compelling model wherein T-cadherin, positioned upstream of DPP4, plays a pivotal role in maintaining a stem-like status within a distinct subpopulation of T-cadherin-expressing cells within MSCs.

Source: Frontiers in Cell and Developmental Biology

DOI: 10.3389/fcell.2025.1734183