AI Article Synopsis

  • The study investigates the role of high-molecular-hyaluronic acid (HMW-HA) as a potential cryoprotectant for human mesenchymal stem cells (hMSCs) to reduce reliance on dimethyl sulfoxide (DMSO).
  • The findings show that while initial cell counts were highest in DMSO, HMW-HA combinations resulted in greater cell proliferation over two weeks, especially with lower DMSO concentrations.
  • Importantly, the addition of HMW-HA did not negatively impact the differentiation potential of the hMSCs, indicating a promising direction for improving cryopreservation methods.

Article Abstract

The physical stresses during cryopreservation affect stem cell survival and further proliferation. To minimize or prevent cryoinjury, cryoprotective agents (CPAs) are indispensable. Despite the widespread use of 10% dimethyl sulfoxide (DMSO), there are concerns about its potential adverse effects. To bypass those effects, combinations of CPAs have been investigated. This study aimed to verify whether high-molecular-hyaluronic acid (HMW-HA) serves as a cryoprotectant when preserving human mesenchymal stem cells (hMSCs) to reduce the DMSO concentration in the cryopreservation medium. We studied how 0.1% or 0.2% HMW-HA combined with reduced DMSO concentrations (from 10% to 5%, and 3%) affected total cell count, viability, immunophenotype, and differentiation potential post-cryopreservation. Immediately after cell revival, the highest total cell count was observed in 10% DMSO-stored hMSC. However, two weeks after cell cultivation an increased cell count was seen in the HMW-HA-stored groups along with a continued increase in hMSCs stored using 3% DMSO and 0.1% HMW-HA. The increased total cell count corresponded to elevated expression of stemness marker CD49f. The HA-supplemented cryomedium did not affect the differential potential of hMSC. Our results will participate in producing a ready-to-use product for cryopreservation of mesenchymal stem cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138570PMC
http://dx.doi.org/10.3390/biom12050610DOI Listing

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