Barzaghini Bianca, Carelli Stephana, Messa Letizia, Rey Federica, Avanzini Maria Antonietta, Jacchetti Emanuela, Maghraby Erika, Berardo Clarissa, Zuccotti Gianvincenzo, Raimondi Manuela Teresa, Cereda Cristina, Calcaterra Valeria, Pelizzo Gloria
Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta," Politecnico Di Milano, Milan, Italy.
Pediatric Research Center "Romeo Ed Enrica Invernizzi," Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Regen Eng Transl Med. 2023 Mar 20:1-12. doi: 10.1007/s40883-023-00296-z.
Mesenchymal stem cells (MSCs) represent a promising source for stem cell therapies in numerous diseases, including pediatric respiratory system diseases. Characterized by low immunogenicity, high anti-inflammatory, and immunoregulatory features, MSCs demonstrated an excellent therapeutic profile in numerous in vitro and preclinical models. MSCs reside in a specialized physiologic microenvironment, characterized by a unique combination of biophysical, biochemical, and cellular properties. The exploitation of the 3D micro-scaffold Nichoid, which simulates the native niche, enhanced the anti-inflammatory potential of stem cells through mechanical stimulation only, overcoming the limitation of biochemical and xenogenic growth factors application.
In this work, we expanded pediatric bone marrow MSCs (BM-MSCs) inside the Nichoid and performed a complete cellular characterization with different approaches including viability assays, immunofluorescence analyses, RNA sequencing, and gene expression analysis.
We demonstrated that BM-MSCs inside the scaffold remain in a stem cell quiescent state mimicking the condition of the in vivo environment. Moreover, the gene expression profile of these cells shows a significant up-regulation of genes involved in immune response when compared with the flat control.
The significant changes in the expression profile of anti-inflammatory genes could potentiate the therapeutic effect of BM-MSCs, encouraging the possible clinical translation for the treatment of pediatric congenital and acquired pulmonary disorders, including post-COVID lung manifestations.
Regenerative medicine is the research field integrating medicine, biology, and biomedical engineering. In this context, stem cells, which are a fundamental cell source able to regenerate tissues and restore damage in the body, are the key component for a regenerative therapeutic approach. When expanded outside the body, stem cells tend to differentiate spontaneously and lose regenerative potential due to external stimuli. For this reason, we exploit the scaffold named Nichoid, which mimics the in vivo cell niche architecture. In this scaffold, mesenchymal stem cells "feel at home" due to the three-dimensional mechanical stimuli, and our findings could be considered as an innovative culture system for the in vitro expansion of stem cells for clinical translation.
The increasing demand of safe and effective cell therapies projects our findings toward the possibility of improving cell therapies based on the use of BM-MSCs, particularly for their clinical translation in lung diseases.
间充质干细胞(MSCs)是众多疾病(包括儿科呼吸系统疾病)干细胞治疗的一个有前景的来源。MSCs具有低免疫原性、高抗炎和免疫调节特性,在众多体外和临床前模型中显示出优异的治疗效果。MSCs存在于一个特殊的生理微环境中,其特征是生物物理、生化和细胞特性的独特组合。利用模拟天然生态位的3D微支架Nichoid,仅通过机械刺激就增强了干细胞的抗炎潜力,克服了生化和异种生长因子应用的局限性。
在这项工作中,我们在Nichoid内扩增儿科骨髓间充质干细胞(BM-MSCs),并采用不同方法进行了完整的细胞表征,包括活力测定、免疫荧光分析、RNA测序和基因表达分析。
我们证明支架内的BM-MSCs保持在干细胞静止状态,模拟体内环境条件。此外,与平板对照相比,这些细胞的基因表达谱显示参与免疫反应的基因显著上调。
抗炎基因表达谱的显著变化可能增强BM-MSCs的治疗效果,鼓励其在治疗儿科先天性和获得性肺部疾病(包括新冠后肺部表现)方面进行临床转化。
再生医学是整合医学、生物学和生物医学工程的研究领域。在这种背景下,干细胞作为能够再生组织和修复身体损伤的基本细胞来源,是再生治疗方法的关键组成部分。当在体外扩增时,干细胞往往会自发分化并因外部刺激而失去再生潜力。因此,我们利用名为Nichoid的支架,它模拟体内细胞生态位结构。在这个支架中,间充质干细胞由于三维机械刺激而“感觉自在”,我们的发现可被视为用于临床转化的干细胞体外扩增的创新培养系统。
对安全有效的细胞治疗的需求不断增加,使我们的研究结果朝着基于BM-MSCs使用改进细胞治疗的可能性发展,特别是在肺部疾病的临床转化方面。