1. Academic Validation
  2. Engineering an organoid culture system for enhanced murine and human hematopoietic stem and progenitor cell self-renewal and expansion

Engineering an organoid culture system for enhanced murine and human hematopoietic stem and progenitor cell self-renewal and expansion

  • Biofabrication. 2025 Oct 24. doi: 10.1088/1758-5090/ae175f.
Keyi Chen 1 Yunqiao Li 2 Xuan Tang 3 Caiping Xu 2 Yunxing Li 2 Xumin Wu 2 Jisheng Li 2 Bowen Zhang 2 Jiahui Zhao 2 Tao Fan 2 Lijuan He 4 Xuetao Pei 2 Yanhua Li 2
Affiliations

Affiliations

  • 1 Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Haidian District, Beijing, China, Beijing, 100850, CHINA.
  • 2 Stem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Haidian District, Beijing, China, Beijing, 100850, CHINA.
  • 3 College of Chemistry & Materials Science, Hebei University, No. 105 Hezuo Road, Beishi District, Baoding City, Hebei Province, China, Baoding, Hebei, 071002, CHINA.
  • 4 Stem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Haidian District, Beijing, China, Beijing, Beijing, 100850, CHINA.
Abstract

Developing a biomimetic culture system is crucial for the efficient maintenance and expansion of rare hematopoietic stem and progenitor cells (HSPCs) in vitro. This advancement can significantly enhance the application of HSPC-based transplantation therapies and support the manufacturing of bone marrow organoids. Traditional two-dimensional culture systems fall short in replicating the interactions between cultured cells and the hematopoietic niche, resulting in excessive Reactive Oxygen Species (ROS) production and triggering HSPC differentiation. In response, we have developed an innovative three-dimensional (3D) culture system using a novel composite hydrogel, GelMA-PVA-TSPBA, which offers excellent biocompatibility and ROS-scavenging properties.
When murine and human embryonic stem cell (hESC)-derived HSPCs were cultured in this new hydrogel, they exhibited low ROS levels and showed enhanced self-renewal and expansion capabilities. Importantly, incorporating niche-related cells into the composite hydrogel created a 3D engineered bone marrow microenvironment that significantly improved the self-renewal and expansion of HSPCs. Additionally, the biomimetic niche comprising GelMA-PVA-TSPBA and various stromal cells effectively inhibited the differentiation of murine and hESC-derived HSPCs. Mechanistically, compared with GelMA, the low ROS microenvironment fostered by GelMA-PVA-TSPBA significantly enhanced mitochondrial function in HSPCs, supporting the expression of HSPC-related genes and inhibiting blood cell differentiation.
Our findings suggest that the GelMA-PVA-TSPBA-based biomimetic culture system has the potential to advance the clinical application of expanded HSPCs and accelerate the development of bone marrow Organoid technology.&#xD.

Keywords

GelMA-PVA-TSPBA hydrogel; Hematopoietic stem/progenitor cells; Reactive oxygen species; expansion; self-renewal.

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