» Articles » PMID: 33923488

Human Adipose Stem Cells (hASCs) Grown on Biodegradable Microcarriers in Serum- and Xeno-Free Medium Preserve Their Undifferentiated Status

Overview
Date 2021 Apr 30
PMID 33923488
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Human adipose stem cells (hASCs) are promising candidates for cell-based therapies, but they need to be efficiently expanded in vitro as they cannot be harvested in sufficient quantities. Recently, dynamic bioreactor systems operated with microcarriers achieved considerable high cell densities. Thus, they are a viable alternative to static planar cultivation systems to obtain high numbers of clinical-grade hASCs. Nevertheless, the production of considerable biomass in a short time must not be achieved to the detriment of the cells' quality. To facilitate the scalable expansion of hASC, we have developed a new serum- and xeno-free medium () and a biodegradable microcarrier (). In this study, we investigated whether the culture of hASCs in defined serum-free conditions on microcarriers (3D) or on planar (2D) cell culture vessels may influence the expression of some marker genes linked with the immature degree or the differentiated status of the cells. Furthermore, we investigated whether the biomaterials, which form our biodegradable MCs, may affect cell behavior and differentiation. The results confirmed that the quality and the undifferentiated status of the hASCs are very well preserved when they grow on MCs in defined serum-free conditions. Indeed, the ASCs showed a gene expression profile more compatible with an undifferentiated status than the same cells grown under standard planar conditions.

Citing Articles

Humanising nanotoxicology: replacement of animal-derived products in the application of integrated approaches to testing and assessment of nanomaterial inhalation hazard.

Fraser R, Campbell K, Pokorski P, MacKinnon E, McAllister K, Neves K Front Bioeng Biotechnol. 2025; 13:1526808.

PMID: 40013306 PMC: 11861073. DOI: 10.3389/fbioe.2025.1526808.


Cellular In Vitro Responses Induced by Human Mesenchymal Stem/Stromal Cell-Derived Extracellular Vesicles Obtained from Suspension Culture.

Souza I, Suzukawa A, Josino R, Marcon B, Robert A, Shigunov P Int J Mol Sci. 2024; 25(14).

PMID: 39062847 PMC: 11277484. DOI: 10.3390/ijms25147605.


Enhancement of therapeutic potential of mesenchymal stem cell by IGF-1 delivery in PLGA microspheres for tissue regeneration.

Ge M, Sun L, Wang D, Hei C, Huang T, Xu Z Regen Ther. 2024; 27:112-119.

PMID: 38550913 PMC: 10973533. DOI: 10.1016/j.reth.2024.03.004.


Emerging Trends in Biodegradable Microcarriers for Therapeutic Applications.

Handral H, Wyrobnik T, Lam A Polymers (Basel). 2023; 15(6).

PMID: 36987266 PMC: 10057597. DOI: 10.3390/polym15061487.


A Review of the Use of Microparticles for Cartilage Tissue Engineering.

Kulchar R, Denzer B, Chavre B, Takegami M, Patterson J Int J Mol Sci. 2021; 22(19).

PMID: 34638629 PMC: 8508725. DOI: 10.3390/ijms221910292.


References
1.
Petrenko Y, Sykova E, Kubinova S . The therapeutic potential of three-dimensional multipotent mesenchymal stromal cell spheroids. Stem Cell Res Ther. 2017; 8(1):94. PMC: 5406927. DOI: 10.1186/s13287-017-0558-6. View

2.
Tan K, Teo K, Lim J, Chen A, Choolani M, Reuveny S . Serum-free media formulations are cell line-specific and require optimization for microcarrier culture. Cytotherapy. 2015; 17(8):1152-65. DOI: 10.1016/j.jcyt.2015.05.001. View

3.
Duan H, Xing S, Luo Y, Feng L, Gramaglia I, Zhang Y . Targeting endothelial CD146 attenuates neuroinflammation by limiting lymphocyte extravasation to the CNS. Sci Rep. 2013; 3:1687. PMC: 3629416. DOI: 10.1038/srep01687. View

4.
Usui T, Murai T, Tanaka T, Yamaguchi K, Nagakubo D, Lee C . Characterization of mac25/angiomodulin expression by high endothelial venule cells in lymphoid tissues and its identification as an inducible marker for activated endothelial cells. Int Immunol. 2002; 14(11):1273-82. DOI: 10.1093/intimm/dxf102. View

5.
Lee M . Hormonal Regulation of Adipogenesis. Compr Physiol. 2017; 7(4):1151-1195. DOI: 10.1002/cphy.c160047. View