Developing a Cell-Microcarrier Tissue-Engineered Product for Muscle Repair Using a Bioreactor System.

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING
Tissue engineering. Part C, Methods Pub Date : 2023-12-01 Epub Date: 2023-11-21 DOI:10.1089/ten.TEC.2023.0122
Ana Luísa Cartaxo, Ana Fernandes-Platzgummer, Carlos A V Rodrigues, Ana M Melo, Katja Tecklenburg, Eva Margreiter, Richard M Day, Cláudia L da Silva, Joaquim M S Cabral
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引用次数: 0

Abstract

Fecal incontinence, although not life-threatening, has a high impact on the economy and patient quality of life. So far, available treatments are based on both surgical and nonsurgical approaches. These can range from changes in diet, to bowel training, or sacral nerve stimulation, but none of which provides a long-term solution. New regenerative medicine-based therapies are emerging, which aim at regenerating the sphincter muscle and restoring continence. Usually, these consist of the administration of a suspension of expanded skeletal-derived muscle cells (SkMDCs) to the damaged site. However, this strategy often results in a reduced cell viability due to the need for cell harvesting from the expansion platform, as well as the non-native use of a cell suspension to deliver the anchorage-dependent cells. In this study, we propose the proof-of-concept for the bioprocessing of a new cell delivery method for the treatment of fecal incontinence, obtained by a scalable two-step process. First, patient-isolated SkMDCs were expanded using planar static culture systems. Second, by using a single-use PBS-MINI Vertical-Wheel® bioreactor, the expanded SkMDCs were combined with biocompatible and biodegradable (i.e., directly implantable) poly(lactic-co-glycolic acid) microcarriers prepared by thermally induced phase separation. This process allowed for up to 80% efficiency of SkMDCs to attach to the microcarriers. Importantly, SkMDCs were viable during all the process and maintained their myogenic features (e.g., expression of the CD56 marker) after adhesion and culture on the microcarriers. When SkMDC-containing microcarriers were placed on a culture dish, cells were able to migrate from the microcarriers onto the culture surface and differentiate into multinucleated myotubes, which highlights their potential to regenerate the damaged sphincter muscle after administration into the patient. Overall, this study proposes an innovative method to attach SkMDCs to biodegradable microcarriers, which can provide a new treatment for fecal incontinence.

使用生物反应器系统开发用于肌肉修复的细胞微载体组织工程产品。
大便失禁虽然不会危及生命,但对经济和患者生活质量有很大影响。到目前为止,可用的治疗方法是基于手术和非手术方法。这些可能包括饮食的改变、肠道训练或骶神经刺激,但都不能提供长期的解决方案。以再生医学为基础的新疗法正在出现,旨在再生括约肌和恢复自制力。通常,这些包括向受损部位施用膨胀的骨骼肌细胞(SkMDCs)的悬浮液。然而,由于需要从扩增平台收获细胞,以及非天然使用细胞悬浮液来递送锚定依赖性细胞,这种策略通常导致细胞活力降低。在这里,我们提出了一种新的细胞递送方法的生物处理概念验证,该方法通过可扩展的两步过程获得,用于治疗大便失禁。首先,使用平面静态培养系统扩增患者分离的SkMDCs。其次,通过使用一次性PBS迷你垂直轮®生物反应器,将膨胀的SkMDCs与生物相容性和可生物降解(即直接植入)的聚乳酸-乙醇酸(PLGA)微载体相结合,该微载体先前通过热诱导相分离(TIPS)制备。该工艺允许SkMDCs附着到微载体上的效率高达80%。重要的是,SkMDCs在所有过程中都是可行的,并在微载体上粘附和培养后保持其肌源性特征(例如CD56标记物的表达)。当将含有微载体的SKMDCs放置在培养皿上时,细胞能够从微载体迁移到培养表面并分化为多核肌管,这突出了它们在给药到患者体内后再生受损括约肌的潜力。总的来说,这项研究提出了一种将SkMDCs连接到可生物降解微载体上的创新方法,这可以为大便失禁提供一种新的治疗方法。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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