Department of Materials Science and Engineering, The Ohio State University, 2041 College Road, Columbus, OH, USA.
Department of Surgery, The Ohio State University, Columbus, OH 43210, USA.
Acta Biomater. 2019 Jan 1;83:96-108. doi: 10.1016/j.actbio.2018.10.038. Epub 2018 Oct 26.
Stem cell therapy is a promising approach to regenerate ischemic cardiovascular tissues yet experiences low efficacy. One of the major causes is inferior cell retention in tissues. Injectable cell carriers that can quickly solidify upon injection into tissues so as to immediately increase viscosity have potential to largely improve cell retention. A family of injectable, fast gelling, and thermosensitive hydrogels were developed for delivering stem cells into heart and skeletal muscle tissues. The hydrogels were also photoluminescent with low photobleaching, allowing for non-invasively tracking hydrogel biodistribution and retention by fluorescent imaging. The hydrogels were polymerized by N-isopropylacrylamide (NIPAAm), 2-hydroxyethyl methacrylate (HEMA), 1-vinyl-2-pyrrolidinone (VP), and acrylate-oligolactide (AOLA), followed by conjugation with hypericin (HYP). The hydrogel solutions had thermal transition temperatures around room temperature, and were readily injectable at 4 °C. The solutions were able to quickly solidify within 7 s at 37 °C. The formed gels were highly flexible possessing similar moduli as the heart and skeletal muscle tissues. In vitro, hydrogel fluorescence intensity decreased proportionally to weight loss. After being injected into thigh muscles, the hydrogel can be detected by an in vivo imaging system for 4 weeks. The hydrogels showed excellent biocompatibility in vitro and in vivo, and can stimulate mesenchymal stem cell (MSC) proliferation and paracrine effects. The fast gelling hydrogel remarkably increased MSC retention in thigh muscles compared to slow gelling collagen, and non-gelling PBS. These hydrogels have potential to efficiently deliver stem cells into tissues. Hydrogel degradation can be non-invasively and real-time tracked. STATEMENT OF SIGNIFICANCE: Low cell retention in tissues represents one of the major causes for limited therapeutic efficacy in stem cell therapy. A family of injectable, fast gelling, and thermosensitive hydrogels that can quickly solidify upon injection into tissues were developed to improve cell retention. The hydrogels were also photoluminescent, allowing for non-invasively and real-time tracking hydrogel biodistribution and retention by fluorescent imaging.
干细胞疗法是一种有前途的方法,可以再生缺血性心血管组织,但疗效较低。其中一个主要原因是细胞在组织中的保留率较低。可在注射到组织中后迅速固化以立即增加粘度的可注射细胞载体有可能大大提高细胞保留率。开发了一系列可注射、快速凝胶化和温度敏感的水凝胶,用于将干细胞递送到心脏和骨骼肌组织中。水凝胶还具有低光漂白的光致发光特性,允许通过荧光成像进行非侵入性跟踪水凝胶的生物分布和保留。水凝胶由 N-异丙基丙烯酰胺 (NIPAAm)、2-羟乙基甲基丙烯酸酯 (HEMA)、1-乙烯基-2-吡咯烷酮 (VP) 和丙烯酸-低聚乳酸 (AOLA) 聚合而成,然后与金丝桃素 (HYP) 缀合。水凝胶溶液的热转变温度接近室温,在 4°C 时很容易注射。溶液在 37°C 下可在 7s 内迅速固化。形成的凝胶具有高度的柔韧性,其模量与心脏和骨骼肌组织相似。在体外,水凝胶的荧光强度与重量损失成比例下降。注入大腿肌肉后,水凝胶可以通过体内成像系统在 4 周内检测到。水凝胶在体外和体内均表现出良好的生物相容性,并能刺激间充质干细胞 (MSC) 的增殖和旁分泌作用。与缓慢凝胶化的胶原和非凝胶化的 PBS 相比,快速凝胶化水凝胶显著提高了 MSC 在大腿肌肉中的保留率。这些水凝胶有可能有效地将干细胞递送到组织中。水凝胶的降解可以进行非侵入性和实时跟踪。
组织中细胞保留率低是干细胞疗法治疗效果有限的主要原因之一。开发了一系列可注射、快速凝胶化和温度敏感的水凝胶,可在注射到组织中后迅速固化,以提高细胞保留率。水凝胶还具有光致发光特性,允许通过荧光成像进行非侵入性和实时跟踪水凝胶的生物分布和保留。