Department of Biomedical Engineering, Stevens Institute of Technology, Hoboken, New Jersey 07030, United States.
Departments of Medicine and Pathology, New York University School of Medicine, New York, New York 10016, United States.
ACS Appl Mater Interfaces. 2022 Nov 23;14(46):51683-51696. doi: 10.1021/acsami.2c13887. Epub 2022 Nov 10.
In recognition of the potential of calreticulin (CRT) protein in enhancing the rate and quality of wound healing in excisional animal wound models, this study was to incorporate CRT via polyblend electrospinning into polycaprolactone (PCL)/type 1 collagen (Col1) nanofibers (NFs; 334 ± 75 nm diameter) as biomimetic extracellular matrices to provide a novel mode of delivery and protection of CRT with enhanced synergistic activities for tissue regeneration. Release kinetic studies using fluoresceinated CRT (CRT-FITC) polyblend NFs showed a burst release within 4 h reaching a plateau at 72 h, with further intervals of release upon incubation with fresh phosphate buffered saline for up to 8 weeks. By measuring fluorescence during the first 4 h of release, CRT-FITC-containing NFs were shown to protect CRT from proteolytic digestion (e.g., by subtilisin) compared to CRT-FITC in solution. CRT incorporated into NFs (CRT-NFs) also showed retention of biological activities and potency for stimulating proliferation and migration of human keratinocytes and fibroblasts. Fibroblasts seeded on CRT-NFs, after 2 days, showed increased amounts of fibronectin, TGF-β1, and integrin β1 in cell lysates by immunoblotting. Compared to NFs without CRT, CRT-NFs supported cell responses consistent with greater cell polarization and increased laminin-5 deposition of keratinocytes and a more motile phenotype of fibroblasts, as suggested by vinculin-capping F-actin fibers nonuniformly located throughout the cell body and the secretion of phosphorylated focal adhesion kinase-enriched migrasomes. Altogether, CRT electrospun into PCL/Col1 NFs retained its structural integrity and biological functions while having additional benefits of customizable loading, protection of CRT from proteolytic degradation, and sustained release of CRT from NFs, coupled with innate physicochemical cues of biomimetic PCL/Col1 NFs. Such synergistic activities have potential for healing recalcitrant wounds such as diabetic foot ulcers.
鉴于钙网蛋白 (CRT) 蛋白在增强切除动物伤口模型中的伤口愈合速度和质量方面的潜力,本研究通过聚 blend 静电纺丝将 CRT 掺入到聚己内酯 (PCL)/I 型胶原蛋白 (Col1) 纳米纤维 (NFs; 334 ± 75nm 直径) 中,作为仿生细胞外基质,提供 CRT 的新型递送和保护方式,并增强协同作用以促进组织再生。使用荧光 CRT (CRT-FITC) 聚 blend NFs 的释放动力学研究显示,在 4 h 内会发生爆发式释放,在 72 h 时达到平台期,在新鲜磷酸盐缓冲液中孵育时会进一步释放,可达 8 周。通过在释放的前 4 h 期间测量荧光强度,与 CRT-FITC 在溶液中的情况相比,CRT-FITC 含量的 NFs 显示出可以保护 CRT 免受蛋白水解酶 (例如枯草杆菌蛋白酶) 的消化。掺入 NFs 中的 CRT (CRT-NFs) 也保留了刺激人角质形成细胞和成纤维细胞增殖和迁移的生物学活性和效力。用免疫印迹法在第 2 天测量细胞裂解物中的纤维连接蛋白、TGF-β1 和整合素 β1 的含量,结果表明成纤维细胞在 CRT-NFs 上接种后,其含量增加。与不含 CRT 的 NFs 相比,CRT-NFs 支持细胞反应,表现为角质形成细胞的细胞极化和层粘连蛋白-5 沉积增加,以及成纤维细胞的运动表型增加,这表现为在整个细胞体内不均匀分布的 vinculin 封闭 F-肌动蛋白纤维和富含磷酸化粘着斑激酶的迁移小体的分泌。总之,静电纺丝到 PCL/Col1 NFs 中的 CRT 保留了其结构完整性和生物学功能,同时具有可定制负载、保护 CRT 免受蛋白水解降解以及从 NFs 中持续释放 CRT 的额外益处,与仿生 PCL/Col1 NFs 的固有物理化学线索相结合。这种协同作用有可能治愈糖尿病足溃疡等难治性伤口。