Towards the Standardization of Mesenchymal Stem Cell Secretome-Derived Product Manufacturing for Tissue Regeneration

被引:38
作者
Chouaib, Batoul [1 ,2 ]
Haack-Sorensen, Mandana [3 ]
Chaubron, Franck [4 ]
Cuisinier, Frederic [1 ,5 ,6 ]
Collart-Dutilleul, Pierre-Yves [1 ,5 ,6 ]
机构
[1] Univ Montpellier, LBN, F-34000 Montpellier, France
[2] IRSN, SERAMED, LRMed, Human Hlth Dept,French Inst Radiol Protect & Nucl, F-92262 Fontenay Aux Roses, France
[3] Univ Copenhagen, Cardiol Stem Cell Ctr 9302, Rigshosp, Henrik Harpestrengsvej 4C, DK-2100 Copenhagen, Denmark
[4] Inst Clinident Biopharm, Biopole Clermont Limagne, F-63360 St Beauzire, France
[5] Univ Montpellier, Fac Dent, F-34000 Montpellier, France
[6] CHU Montpellier, Serv Odontol, F-34000 Montpellier, France
关键词
mesenchymal stem cell; secretome; manufacturing; tissue regeneration; MARROW STROMAL CELLS; CONDITIONED MEDIUM; PASSAGE NUMBER; EXTRACELLULAR VESICLES; STEM/STROMAL CELLS; MIGRATION; ENHANCE; EXOSOMES; INJURY; REPAIR;
D O I
10.3390/ijms241612594
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cell secretome or conditioned medium (MSC-CM) is a combination of biomolecules and growth factors in cell culture growth medium, secreted by mesenchymal stem cells (MSCs), and the starting point of several derived products. MSC-CM and its derivatives could be applied after injuries and could mediate most of the beneficial regenerative effects of MSCs without the possible side effects of using MSCs themselves. However, before the clinical application of these promising biopharmaceuticals, several issues such as manufacturing protocols and quality control must be addressed. This review aims to underline the influence of the procedure for conditioned medium production on the quality of the secretome and its derivatives and highlights the questions considering cell sources and donors, cell expansion, cell passage number and confluency, conditioning period, cell culture medium, microenvironment cues, and secretome-derived product purification. A high degree of variability in MSC secretomes is revealed based on these parameters, confirming the need to standardize and optimize protocols. Understanding how bioprocessing and manufacturing conditions interact to determine the quantity, quality, and profile of MSC-CM is essential to the development of good manufacturing practice (GMP)-compliant procedures suitable for replacing mesenchymal stem cells in regenerative medicine.
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页数:15
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