In vivo real-time visualization of mesenchymal stem cells tropism for cutaneous regeneration using NIR-II fluorescence imaging

间充质干细胞 归巢(生物学) 伤口愈合 生物医学工程 材料科学 体内 脚手架 再生(生物学) 干细胞 新生血管 荧光寿命成像显微镜 移植 病理 医学 细胞生物学 外科 血管生成 癌症研究 荧光 生物 生态学 物理 生物技术 量子力学
作者
Guangcun Chen,Fei Tian,Chunyan Li,Yejun Zhang,Zhen Weng,Yan Zhang,Rui Peng,Qiangbin Wang
出处
期刊:Biomaterials [Elsevier BV]
卷期号:53: 265-273 被引量:98
标识
DOI:10.1016/j.biomaterials.2015.02.090
摘要

Mesenchymal stem cells (MSCs) have shown great potential for cutaneous wound regeneration in clinical practice. However, the in vivo homing behavior of intravenously transplanted MSCs to the wounds is still poorly understood. In this work, fluorescence imaging with Ag2S quantum dots (QDs) in the second near-infrared (NIR-II) window was performed to visualize the dynamic homing behavior of transplanted human mesenchymal stem cells (hMSCs) to a cutaneous wound in mice. Benefiting from the desirable spatial and temporal resolution of Ag2S QDs-based NIR-II imaging, for the first time, the migration of hMSCs to the wound was dynamically visualized in vivo. By transplanting a blank collagen scaffold in the wound to help the healing, it was found that hMSCs were slowly recruited at the wound after intravenous injection and were predominantly accumulated around the edge of wound. This resulted in poor healing effects in terms of slow wound closure and thin thickness of the regenerated skin. In contrast, for the wound treated by the collagen scaffold loaded with stromal cell derived factor-1α (SDF-1α), more hMSCs were recruited at the wound within a much shorter time and were homogenously distributed across the whole wound area, which enhances the re-epithelialization, the neovascularization, and accelerates the wound healing.
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