Potential of Fibrin Glue and Mesenchymal Stem Cells (MSCs) to Regenerate Nerve Injuries: A Systematic Review.
Adriana De Cássia OrtizSimone Ortiz Moura FidelesKarina Torres PominiMárcia Zilioli BelliniEliana de Souza Bastos Mazuqueli PereiraCarlos Henrique Bertoni ReisJoão Paulo Galletti PilonMiguel Ângelo de MarchiBeatriz Flavia de Moraes TrazziWillian Saranholi da SilvaMarcelo Rodrigues da CunhaDaniela Vieira BuchaimRogério Leone BuchaimPublished in: Cells (2022)
Cell-based therapy is a promising treatment to favor tissue healing through less invasive strategies. Mesenchymal stem cells (MSCs) highlighted as potential candidates due to their angiogenic, anti-apoptotic and immunomodulatory properties, in addition to their ability to differentiate into several specialized cell lines. Cells can be carried through a biological delivery system, such as fibrin glue, which acts as a temporary matrix that favors cell-matrix interactions and allows local and paracrine functions of MSCs. Thus, the aim of this systematic review was to evaluate the potential of fibrin glue combined with MSCs in nerve regeneration. The bibliographic search was performed in the PubMed/MEDLINE, Web of Science and Embase databases, using the descriptors ("fibrin sealant" OR "fibrin glue") AND "stem cells" AND "nerve regeneration", considering articles published until 2021. To compose this review, 13 in vivo studies were selected, according to the eligibility criteria. MSCs favored axonal regeneration, remyelination of nerve fibers, as well as promoted an increase in the number of myelinated fibers, myelin sheath thickness, number of axons and expression of growth factors, with significant improvement in motor function recovery. This systematic review showed clear evidence that fibrin glue combined with MSCs has the potential to regenerate nervous system lesions.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- stem cells
- systematic review
- cell therapy
- bone marrow
- meta analyses
- platelet rich plasma
- single cell
- peripheral nerve
- induced apoptosis
- poor prognosis
- spinal cord injury
- multiple sclerosis
- cell death
- signaling pathway
- risk assessment
- deep learning
- pi k akt
- white matter
- long non coding rna
- cell proliferation