TY - JOUR
T1 - Characterization and Proteomic Profiling of Hepatocyte-like Cells Derived from Human Wharton’s Jelly Mesenchymal Stromal Cells
T2 - De Novo Expression of Liver-Specific Enzymes
AU - Lo Iacono, Melania
AU - Corrao, Simona
AU - Alberti, Giusi
AU - Amico, Giandomenico
AU - Timoneri, Francesca
AU - Russo, Eleonora
AU - Cucina, Annamaria
AU - Indelicato, Sergio
AU - Rappa, Francesca
AU - Corsello, Tiziana
AU - Saieva, Salvatore
AU - Di Stefano, Antonino
AU - Di Gaudio, Francesca
AU - Conaldi, Pier Giulio
AU - La Rocca, Giampiero
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/2
Y1 - 2025/2
N2 - Liver transplantation is the only therapeutic option for patients affected by end-stage liver disease (ESLD), but its feasibility is restricted by the shortage of donated organs. Stem cell therapy could represent a valid treatment option for these conditions. In particular, the mesenchymal stromal cells derived from the human umbilical cord matrix (WJ-MSCs), thanks to their specific features, can be considered good candidates for liver tissue repair and regeneration. We found that the WJ-MSCs differentiate in hepatocyte-like cells (HLCs) using a differentiation protocol that resembles the in vivo liver morphogenesis. We also showed that HLCs acquired mature hepatic functions and maintained their intrinsic hypoimmunogenicity, a key feature to avoid rejection in the host. Moreover, thanks to proteomic analysis, we highlighted several hepatic proteins in HLCs, demonstrating that these cells could be valid candidates for the treatment of ESLD.
AB - Liver transplantation is the only therapeutic option for patients affected by end-stage liver disease (ESLD), but its feasibility is restricted by the shortage of donated organs. Stem cell therapy could represent a valid treatment option for these conditions. In particular, the mesenchymal stromal cells derived from the human umbilical cord matrix (WJ-MSCs), thanks to their specific features, can be considered good candidates for liver tissue repair and regeneration. We found that the WJ-MSCs differentiate in hepatocyte-like cells (HLCs) using a differentiation protocol that resembles the in vivo liver morphogenesis. We also showed that HLCs acquired mature hepatic functions and maintained their intrinsic hypoimmunogenicity, a key feature to avoid rejection in the host. Moreover, thanks to proteomic analysis, we highlighted several hepatic proteins in HLCs, demonstrating that these cells could be valid candidates for the treatment of ESLD.
KW - cell therapy
KW - hepatic failure
KW - hepatocyte differentiation
KW - hypoimmunogenicity
KW - immune modulation
KW - liver diseases
KW - perinatal stem cells
KW - umbilical cord
KW - Wharton’s jelly mesenchymal stromal cells
UR - http://www.scopus.com/inward/record.url?scp=85219202853&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85219202853&partnerID=8YFLogxK
U2 - 10.3390/biology14020124
DO - 10.3390/biology14020124
M3 - Article
C2 - 40001892
AN - SCOPUS:85219202853
SN - 2079-7737
VL - 14
JO - Biology
JF - Biology
IS - 2
M1 - 124
ER -