School of Veterinary Medicine and Animal Sciences, University of São Paulo, São Paulo 05508-220, SP, Brazil.
Post-Graduate Program in Biophotonics Applied to Health Sciences, Nove de Julho University (UNINOVE), São Paulo 17011-102, SP, Brazil.
Int J Mol Sci. 2024 Sep 20;25(18):10131. doi: 10.3390/ijms251810131.
Several lung diseases can cause structural damage, making lung transplantation the only therapeutic option for advanced disease stages. However, the transplantation success rate remains limited. Lung bioengineering using the natural extracellular matrix (ECM) of decellularized lungs is a potential alternative. The use of undifferentiated cells to seed the ECM is practical; however, sterilizing the organ for recellularization is challenging. Photobiomodulation therapy (PBMT) may offer a solution, in which the wavelength is crucial for tissue penetration. This study aimed to explore the potential of optimizing lung recellularization with mesenchymal stem cells using PBMT (660 nm) after sterilization with PBMT (880 nm). The lungs from C57BL/6 mice were decellularized using 1% SDS and sterilized using PBMT (880 nm, 100 mW, 30 s). Recellularization was performed in two groups: (1) recellularized lung and (2) recellularized lung + 660 nm PBMT (660 nm, 100 mW, 30 s). Both were seeded with mesenchymal stem cells from human tooth pulp (DPSc) and incubated for 24 h at 37 °C and 5% CO in bioreactor-like conditions with continuous positive airway pressure (CPAP) at 20 cmHO and 90% O. The culture medium was analyzed after 24 h. H&E, immunostaining, SEM, and ELISA assays were performed. Viable biological scaffolds were produced, which were free of cell DNA and preserved the glycosaminoglycans; collagens I, III, and IV; fibronectin; laminin; elastin; and the lung structure (SEM). The IL-6 and IL-8 levels were stable during the 24 h culture, but the IFN-γ levels showed significant differences in the recellularized lung and recellularized lung + 660 nm PBMT groups. Greater immunological modulation was observed in the recellularized groups regarding pro-inflammatory cytokines (IL-6, IFN-γ, and IL-8). These findings suggest that PBMT plays a role in cytokine regulation and antimicrobial activity, thus offering promise for enhanced therapeutic strategies in lung bioengineering.
几种肺部疾病可导致结构损伤,使肺移植成为晚期疾病阶段的唯一治疗选择。然而,移植成功率仍然有限。使用脱细胞化肺的天然细胞外基质(ECM)进行肺生物工程是一种潜在的替代方法。使用未分化细胞接种 ECM 是可行的;然而,为了再细胞化而对器官进行消毒是具有挑战性的。光生物调节疗法(PBMT)可能是一种解决方案,其中波长对于组织穿透至关重要。本研究旨在探索使用 PBMT(660nm)对脱细胞化肺进行消毒后,使用 PBMT(660nm)优化间充质干细胞肺再细胞化的潜力(880nm,100mW,30s)。使用 1%SDS 对 C57BL/6 小鼠的肺进行脱细胞化,并用 PBMT(880nm,100mW,30s)进行消毒。再细胞化在两组中进行:(1)再细胞化肺和(2)再细胞化肺+660nm PBMT(660nm,100mW,30s)。两组均接种人牙髓间充质干细胞(DPSc),并在生物反应器样条件下在 37°C 和 5%CO 下孵育 24 小时,持续气道正压(CPAP)为 20cmHO 和 90%O。在 24 小时后分析培养物。进行 H&E、免疫染色、SEM 和 ELISA 测定。生成了有活力的生物支架,这些支架不含细胞 DNA,并保留了糖胺聚糖;I、III 和 IV 型胶原蛋白;纤连蛋白;层粘连蛋白;弹性蛋白;和肺结构(SEM)。在 24 小时的培养过程中,IL-6 和 IL-8 水平保持稳定,但 IFN-γ 水平在再细胞化肺和再细胞化肺+660nm PBMT 组中存在显著差异。在再细胞化组中观察到针对促炎细胞因子(IL-6、IFN-γ 和 IL-8)的更大免疫调节作用。这些发现表明 PBMT 在细胞因子调节和抗菌活性中发挥作用,因此为肺生物工程中的增强治疗策略提供了希望。