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April 19, 2026Nature Biomedical Engineering3 citationsOpen Access

Three-dimensional quantitative tissue clearing reveals differences in osteovascular niche of aged and young human mesenchymal stromal cells

NCNelson Tsz Long ChuODOstap DregvalYCYu-Wei Chang

Key Points

  • This research aims to understand the differences in the microenvironment of mesenchymal stem cells in young versus aged human bones.
  • Introduced a tissue-clearing protocol called DeepBone for human bones.
  • Integrated mRNA and protein detection in the tissue-clearing process.
  • Spatially mapped BM-MSCs relative to blood vessels, adipocytes, sinusoids, and bony trabeculae.
  • Young bone microenvironments are rich in vasculature, sinusoids, and adipocytes.
  • Aged bone microenvironments show no preferential association of BM-MSCs with bone or adipocytes.
  • Proliferative BM-MSCs are primarily found near blood vessels.
  • Identified a specialized microenvironment for BM-MSCs in young bone enriched with R-type vessels.

Abstract

Abstract Human bone marrow mesenchymal stromal/stem cells (BM-MSCs) are widely used in clinical trials and tissue engineering, yet their native microenvironment remains poorly understood. Here we introduce a tissue-clearing protocol, DeepBone, for human bones and integrate it with simultaneous mRNA and protein detection. Using this protocol, we spatially map BM-MSCs relative to key bone microenvironment components, including human blood capillaries, adipocytes, sinusoids and bony trabeculae. Quantitative analysis reveals 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 show no preferential association with bone or adipocytes. Proliferative BM-MSCs are predominantly found along blood vessels. Moreover, we identify a specialized microenvironment for BM-MSCs in young bone, characterized by sinusoids coiled around trabeculae and enriched by R-type vessels. These findings provide insights into the native niches of BM-MSCs, offering a foundation for the development of tissue engineering strategies that mimic their physiological context.

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Cite This Study

Chu et al. (2026) studied this question.

synapsesocial.com/papers/69e4741c010ef96374d8fd3dhttps://doi.org/10.1038/s41551-026-01645-3
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