Developing a Cell-Microcarrier Tissue-Engineered Product for Muscle Repair Using a Bioreactor System
TISSUE ENGINEERING PART C-METHODS(2023)
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 (R) 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. Impact statementAt present, no life-long treatment for fecal incontinence exists. New regenerative medicine-based therapies can be seen as a new avenue to solve this burdening health situation. Our approach relies on the administration of implantable biodegradable microcarriers that deliver cells capable of regenerating muscle to the damaged sphincter. In this study, we demonstrate the feasibility of using single-use, bioreactor technology for developing a cell-microcarrier combined product. Moreover, we show that the microcarrier-attached cells, due to their differentiation capacity and the presence of myogenic markers, display muscle regenerative potential, and are likely to be able to provide life-lasting repairs to the damaged muscle.
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Key words
fecal incontinence,skeletal derived muscle cells,TIPS PLGA microcarriers,myotube formation,CD56
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