Research Paper Volume 16, Issue 9 pp 7928—7945

Human umbilical cord mesenchymal stem cells promote steroid-induced osteonecrosis of the femoral head repair by improving microvascular endothelial cell function

Junwen Chen1, *, , Wenyi Jin1,2, *, , Changheng Zhong1, *, , Wenxiang Cai1, , Liangkun Huang1, , Jianlin Zhou1, , Hao Peng1, ,

  • 1 Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan 430062, China
  • 2 Department of Biomedical Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong 999077, Hong Kong Special Administrative Region
* Equal contribution

Received: January 3, 2024       Accepted: April 10, 2024       Published: April 29, 2024      

https://doi.org/10.18632/aging.205794
How to Cite

Copyright: © 2024 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Recently, there has been growing interest in using cell therapy through core decompression (CD) to treat osteonecrosis of the femoral head (ONFH). Our study aimed to investigate the effectiveness and mechanism of human umbilical cord mesenchymal stem cells (hUCMSCs) in treating steroid-induced ONFH. We constructed a steroid-induced ONFH rabbit model as well as dexamethasone (Dex)-treated bone microvascular endothelial cells (BMECs) model of human femoral head. We injected hUCMSCs into the rabbit femoral head via CD. The effects of hUCMSCs on steroid-induced ONFH rabbit model and Dex-treated BMECs were evaluated via micro-CT, microangiography, histology, immunohistochemistry, wound healing, tube formation, and western blotting assay. Furthermore, we conducted single-cell RNA sequencing (scRNA-seq) to examine the characteristics of endothelial cells, the activation of signaling pathways, and inter-cellular communication in ONFH. Our data reveal that hUCMSCs improved the femoral head microstructure and bone repair and promoted angiogenesis in the steroid-induced ONFH rabbit model. Importantly, hUCMSCs improved the migration ability and angioplasty of Dex-treated BMECs by secreting COL6A2 to activate FAK/PI3K/AKT signaling pathway via integrin α1β1.

Abbreviations

CD: core decompression; ONFH: osteonecrosis of the femoral head; hUCMSCs: human umbilical cord mesenchymal stem cells; Dex: dexamethasone; BMECs: bone microvascular endothelial cells; scRNA-seq: single-cell RNA sequencing; ECs: endothelial cells; MSC: Mesenchymal stem cell; MPS: methylprednisolone; LPS: lipopolysaccharide; BV/TV: bone volume/total volume; Tb.N: trabecular number; Tb.Sp: trabecular separation; Tb.Th: trabecular thickness; GO: gene ontology; DEGs: differentially expressed genes; KEGG: Kyoto Encyclopedia of Genes and Genomes; HE: hematoxylin and eosin.