脊髓损伤
脚手架
干细胞
神经炎症
生物医学工程
脊髓
细胞生物学
材料科学
化学
神经科学
医学
炎症
生物
免疫学
作者
Chen Qiu,Yuan Sun,Jinying Li,Jiayi Zhou,Yan Xu,Cong Qiu,Yu Kang,Ling Jia,Yuan‐Qing Jiang,Wenyu Cui,Guanghao Wang,Lei He,Weixin Yuan,Jun‐Ming Tang,Yaohui Kou,Ge Zhang,Zhiying He,Shaomin Zhang,Yong He,Luyang Yu
标识
DOI:10.1002/advs.202301639
摘要
Stem cells play critical roles in cell therapies and tissue engineering for nerve repair. However, achieving effective delivery of high cell density remains a challenge. Here, a novel cell delivery platform termed the hyper expansion scaffold (HES) is developed to enable high cell loading. HES facilitated self-promoted and efficient cell absorption via a dual driving force model. In vitro tests revealed that the HES rapidly expanded 80-fold in size upon absorbing 2.6 million human amniotic epithelial stem cells (hAESCs) within 2 min, representing over a 400% increase in loading capacity versus controls. This enhanced uptake benefited from macroscopic swelling forces as well as microscale capillary action. In spinal cord injury (SCI) rats, HES-hAESCs promoted functional recovery and axonal projection by reducing neuroinflammation and improving the neurotrophic microenvironment surrounding the lesions. In summary, the dual driving forces model provides a new rationale for engineering hydrogel scaffolds to facilitate self-promoted cell absorption. The HES platform demonstrates great potential as a powerful and efficient vehicle for delivering high densities of hAESCs to promote clinical treatment and repair of SCI.
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