1. Academic Validation
  2. Immunomodulatory property and its regulatory mechanism of double network hydrogel on dendritic cells

Immunomodulatory property and its regulatory mechanism of double network hydrogel on dendritic cells

  • J Biomed Mater Res A. 2021 Jun;109(6):1015-1026. doi: 10.1002/jbm.a.37091.
Fujun Zhu 1 2 3 Yalin Tong 3 Yao Wu 2 Ning Dong 2 Zhiyong Sheng 1 2 Yongming Yao 1 2
Affiliations

Affiliations

  • 1 Chinese PLA General Hospital and Medical School of Chinese PLA, Beijing, China.
  • 2 Trauma Research Center, Fourth Medical Center and Medical Innovation Research Department of Chinese PLA General Hospital, Beijing, China.
  • 3 Department of Burns, Plastic, and Wound Repair Surgery, The 924th Hospital of the Joint Logistic Support Force of Chinese PLA, Guilin, China.
Abstract

Modulation of the key immune cell subsets by biomaterial has emerged as a potential target to promote tissue repair and regeneration. Based on calcium alginate (Alg) and glycol chitosan (GC), an injectable double-network (DN) hydrogel has been developed as a scaffold for cell delivery and cell cocultured system. Previous studies have documented the interaction between dendritic cells (DCs) and GC or Alg hydrogel, but the potential effect of DN hydrogel on activation of DCs still remains unclear. This research was conducted to explore the immunomodulatory influence and underlying mechanisms of GC/Alg DN hydrogel on DCs in vitro and in vivo. Stimulation of DCs with DN hydrogel obviously induced the maturation of DCs in vitro. In vivo, DN hydrogel did not have obvious influence on the maturation of splenic DCs on postimplantation days 3, 10, and 30. Mechanistically, we found that DN hydrogel induced the maturation of DCs via phosphorylation of phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin in vitro. It provides a novel understanding of the immunomodulatory property of DN hydrogel on DCs, which may serve as potential target for designing immune-mediated regenerative strategies.

Keywords

dendritic cells; double-network hydrogel; immune modulation; implantation; signaling pathway.

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