Spinal cord decellularized matrix scaffold loaded with engineered basic fibroblast growth factor-overexpressed human umbilical cord mesenchymal stromal cells promoted the recovery of spinal cord injury.
Wenli HeChunying ShiJia YinFeifei HuangWenjing YanJin DengBing ZhangBin WangHaiping WangPublished in: Journal of biomedical materials research. Part B, Applied biomaterials (2022)
Spinal cord injury (SCI) will lead to irreversible damage of sensory and motor function of central nervous system, which seriously affects patient's quality of life. A variety of nerve engineering materials carrying various stem cells and cell growth factors had used to promote the repair of SCI, but they could not mimic the actual matric niche at spinal cord to promote cell proliferation and differentiation. Thus, developing novel biomaterial providing better niche of spinal cord is a new strategy to treat the severe SCI. In this study, we constructed porcine spinal cord decellularized matrix scaffold (SC-DM) with biocompatibility to load engineered basic fibroblast growth factor-overexpressing human umbilical cord mesenchymal stromal cells (bFGF-HUCMSCs) for treating SCI. The continuously released bioactive bFGF factors from grafted bFGF-HUCMSCs and three-dimensional niche by SC-DM promoted the differentiation of endogenous stem cells into neurons with nerve conduction function, leading a markedly motor function recovery of SCI. These results indicated that the functional bFGF-HUCMSCs/SC-DM scaffold provided more suitable matric niche for nerve cells, that would be a promising strategy for the clinical application of SCI.
Keyphrases
- spinal cord injury
- spinal cord
- umbilical cord
- tissue engineering
- mesenchymal stem cells
- stem cells
- neuropathic pain
- endothelial cells
- cell proliferation
- bone marrow
- cell therapy
- induced apoptosis
- peripheral nerve
- drug delivery
- induced pluripotent stem cells
- extracellular matrix
- type diabetes
- early onset
- oxidative stress
- pluripotent stem cells
- cell cycle
- wastewater treatment
- endoplasmic reticulum stress
- cancer therapy
- skeletal muscle
- adipose tissue
- insulin resistance
- weight loss