Unveiling the phenotypic impact of cryopreservation on adipose derived stem cells: A systematic review
Background & objectivesThe impact of cell passaging and cryopreservation on the phenotypic and functional attributes of adipose-derived stem cells (ADSCs) must be understood to improve their clinical value. This systematic review investigates the phenotypic characteristics of ADSCs derived from fresh and cryopreserved adipose tissue, with a focus on how these cells change across passages. MethodsA thorough search of databases was conducted as per the PRISMA guideline to find publications that were aligned with the inclusion criteria and were published between January 2013 and January 2023. ResultsIn both cryopreserved and fresh stromal vascular fraction (SVF) cells, CD90, CD73, and CD105 consistently exhibited strong expression (90%) across passages in 50 screened studies. In fresh tissue, CD29 was upregulated in subsequent passages (up to 95%) but downregulated at passage 2 (2.3%). Variable CD29 was seen in cryopreserved groups (47% at P1, 90% at P4). While CD34 and CD45 were lower in cryopreserved ADSCs (less than 5%), they were higher in fresh tissue (41%), suggesting less haematopoietic contamination. Interpretation & conclusionsPassaging and cryopreservation protocols can help maintain the therapeutic potential of ADSCs, providing a reliable source of functional stem cells for regenerative utilization.
Authors
- Sadia Farhana (ORCID: https://orcid.org/0000-0002-7510-6462)
- Mohd Zulkifli Salleh (ORCID: https://orcid.org/0000-0003-4069-9381)
- Nur Azida Mohd Nasir (ORCID: https://orcid.org/0000-0003-0110-1316)
- Shazana Hilda Shamsuddin (ORCID: https://orcid.org/0000-0001-6466-2271)
- Wan Azman Wan Sulaiman (ORCID: https://orcid.org/0000-0002-0600-9765)
Institutions
- Universiti Sains Malaysia (MY)
Publication Details
- Journal
- The Indian Journal of Medical Research
- Published
- 2025-12-08
- DOI
- https://doi.org/10.25259/ijmr_686_2025
- Primary Topic
- Mesenchymal stem cell research
- Type
- article
- Field-Weighted Citation Impact
- 0.00