Vascular restoration through local delivery of angiogenic factors stimulates bone regeneration in critical size defects.
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ABSTRACT: Critical size bone defects represent a significant challenge worldwide, often leading to persistent pain and physical disability that profoundly impact patients' quality of life and mental well-being. To address the intricate and complex repair processes involved in these defects, we performed single-cell RNA sequencing and revealed notable shifts in cellular populations within regenerative tissue. Specifically, we observed a decrease in progenitor lineage cells and endothelial cells, coupled with an increase in fibrotic lineage cells and pro-inflammatory cells within regenerative tissue. Furthermore, our analysis of differentially expressed genes and associated signaling pathway at the single-cell level highlighted impaired angiogenesis as a central pathway in critical size bone defects,
SUBMITTER: Fang L
PROVIDER: S-EPMC11295624 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature
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