Department of Respiratory Diseases, Clinical Center for Molecular Diagnosis and Therapy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000, China.
Department of Respiratory Diseases, Clinical Center for Molecular Diagnosis and Therapy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000, China.
Biomater Adv. 2022 Jun;137:212817. doi: 10.1016/j.bioadv.2022.212817. Epub 2022 Apr 22.
Bronchial and pleural injuries with persistent air leak pose a threat in the repair and regeneration of pulmonary diseases. The need to arrive at a highly efficient therapy for closure of bronchopleural fistula (BPF) so as to effectively suppress inflammation, infection and repair the damaged pleural space caused by cancer as well as contractile restoration of bronchopleural scars remain a significant clinical challenge. Herein, we have designed and developed potent bioactive vitamin K3 carnosine peptide (VKC)-loaded spun SF fibroin fibers/collagen bi-layered 3D scaffold for bronchopleural fistula tissue engineering applications. The VKC drug showed excellent cell viability in human bronchial epithelial cells (HBECs), in addition to its pronounced higher cytotoxicity against the A549 lung cancer cell line with an IC of 5 μg/mL. Furthermore, VKC displayed a strong affinity with the catalytic site of EGFR (PDB ID: 1M17) and VEGFR2 (PDB ID: 4AGD, 4ASD) receptors in molecular docking studies. Following which the spun SF-VKC (primary layer) and collagen film (top layer) constructed bi-layered CSVKC were structurally elucidated and its morphological, physicochemical and biological characterizations were well examined. The bi-layered scaffold showed superior biocompatibility and cell migration ability in HBECs than other scaffolds. Interestingly, the CSVKC revealed rapid HBECs motility towards scratched regions for fast healing in vitro bronchial tissue engineering. In vivo biocompatibility and angiogenesis studies of the prepared scaffolds were evaluated and the results obtained demonstrated excellent new tissue formation and neovascularization in the bi-layered architecture rather than others. Therefore, our results suggest that the potent antibacterial and anticancer therapeutic agent (VKC)-impregnated silk fibroin fibers/collagen bi-layered 3D biomaterial could be useful in treating cancerous BPF and pulmonary diseases in future.
支气管和胸膜损伤伴持续漏气对肺部疾病的修复和再生构成威胁。需要找到一种高效的治疗方法来闭合支气管胸膜瘘(BPF),以有效抑制炎症、感染,并修复癌症引起的受损胸膜空间以及支气管胸膜瘢痕的收缩性恢复,这仍然是一个重大的临床挑战。在此,我们设计并开发了一种有效的生物活性维生素 K3 肉碱肽(VKC)负载纺丝 SF 丝素纤维/胶原蛋白双层 3D 支架,用于支气管胸膜瘘组织工程应用。VKC 药物在人支气管上皮细胞(HBEC)中表现出优异的细胞活力,此外,它对 A549 肺癌细胞系的细胞毒性也明显更高,IC 为 5μg/mL。此外,VKC 在分子对接研究中显示出与 EGFR(PDB ID:1M17)和 VEGFR2(PDB ID:4AGD、4ASD)受体的催化位点具有很强的亲和力。随后,对纺丝 SF-VKC(基层)和胶原蛋白膜(顶层)构建的双层 CSVKC 进行了结构阐明,并对其形态、理化和生物学特性进行了全面研究。与其他支架相比,双层支架在 HBECs 中表现出更好的生物相容性和细胞迁移能力。有趣的是,CSVKC 显示出 HBECs 向划痕区域快速迁移的能力,以便在体外快速愈合支气管组织工程。对制备的支架进行了体内生物相容性和血管生成研究,结果表明双层结构具有优异的新组织形成和血管生成能力,优于其他结构。因此,我们的结果表明,载有强力抗菌和抗癌治疗剂(VKC)的丝素纤维/胶原蛋白双层 3D 生物材料可用于未来治疗癌性 BPF 和肺部疾病。