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Biology subjects

Dregval, O.

Publications and source records attributed to Dregval, O..

2 recordsLinked to original sources

Quantitative Multicolored Deep Imaging of Human Bones Reveals a Composite Osteo-Sinusoidal Niche for Mesenchymal Stromal Cells.

Human bone marrow mesenchymal stromal/stem cells (BM-MSCs) are widely utilized in clinical trials and tissue engineering; however, their native microenvironment remains poorly understood. Here, we introduced a tissue-clearing protocol for human bones and integrated it with simultaneous mRNA and protein detection. Using this protocol, named DeepBone, we spatially mapped BM-MSCs relative to key bone microenvironment components, including human blood capillaries, adipocytes, sinusoids, and bony trabeculae. Quantitative analysis revealed that the native microenvironment of human BM-MSCs in young bone is enriched in vasculature, sinusoids, bone matrix, and adipocytes. In contrast, in aged bone, BM-MSCs showed no preferential association with bone or adipocytes. Proliferative BM-MSCs were predominantly found along blood vessels. Moreover, we identified a specialized microenvironment for BM-MCs in young bone, characterized by sinusoids coiled around trabeculae and enriched by R-type vessels. These findings provide novel insights into the native niches of BM-MSCs, offering a foundation for the development of tissue-engineering strategies that mimic their physiological context.

cell biology↗

A transcriptional atlas of the pubertal human growth plate reveals direct stimulation of cartilage stem cells by growth hormone.

The cartilaginous growth plate is a critical organ responsible for longitudinal bone growth. It remains open throughout life in mice but closes in humans after puberty. Growth hormone (GH) is a widely used therapy for children with growth retardation and open growth plates. However, it remains unclear whether GH directly targets human growth plates. Furthermore, while cartilage stem cells have recently been identified in mouse growth plates, their presence and GH responsiveness in human growth plates are unknown. To address these gaps, we characterized the cellular and molecular organization of early pubertal human growth plates using unique tissue samples obtained during growth-restricting surgeries. Our analysis identified two distinct populations of stem cells differing in cycling activity, molecular profiles, and regulatory factors. Quiescent stem cells were localized within a niche characterized by low Wnt and TGF{beta} signaling. To investigate the direct effects of GH, we developed a human growth plate explant culture system. GH directly stimulated explant growth and promoted stem cell proliferation by activating the JAK/STAT, TGF{beta}, and ERK pathways while inhibiting the AKT pathway. Notably, activation of the TGF{beta} pathway occurred in an autocrine manner. These findings provide critical new insights into human longitudinal growth and the mechanisms of GH action, with potential implications for optimizing treatments for growth disorders. One Sentence SummaryThis study reveals that growth hormone (GH) directly promotes proliferation within the human growth plate and activates TGF{beta} and ERK signaling pathways in cartilage stem cells, providing critical insights into human longitudinal growth and potential improvements in treatments for growth disorders.

cell biology↗