TY - JOUR
T1 - Omics Reveals Signaling-Associated Traits of Extracellular Vesicles Derived from Dental Stem Cells
AU - Wang, Miao
AU - Tong, Wai Man
AU - Ma, Shuyu
AU - Yu, Yiru
AU - Guo, Can
AU - Zhou, Shuo
AU - Xu, Dan
AU - Li, Ye
N1 - Publisher Copyright:
© 2026 SAGE Publications.
PY - 2026
Y1 - 2026
N2 - Stem cell-derived extracellular vesicles (EVs) play a crucial role in intercellular communication and reflect the functional characteristics of their parent cells. Despite the significant therapeutic potential of these EVs, the molecular features of EVs derived from different stem cells and their relationship with tissue specificity remain underexplored. In this study, we conducted integrated proteomic and transcriptomic analyses of EVs derived from six dental stem cells (DSCs) and three systemic stem cells (SSCs) to investigate the role of EVs in tissue-specific molecular transfer. This study found that although DSCs and SSCs share 92.1% of the core proteome, the EVs derived from each stem cell type displayed distinct molecular signatures. EVs from DSCs were enriched in signaling molecules, reflecting their parent cells’ roles in local tissue repair, whereas EVs from SSCs carried mitochondrial and metabolic proteins, indicating their preferential involvement in metabolic regulation. Furthermore, we uncovered that the parent cells transferred 83% of the core proteins to their EVs in a tissue-specific pattern, ensuring that dental EVs retain prominent signaling functions. Thus, understanding the relationship between EVs and their parent stem cells with respect to tissue origin would be helpful to harness EVs as targeted therapeutic agents, particularly in oral regenerative medicine.
AB - Stem cell-derived extracellular vesicles (EVs) play a crucial role in intercellular communication and reflect the functional characteristics of their parent cells. Despite the significant therapeutic potential of these EVs, the molecular features of EVs derived from different stem cells and their relationship with tissue specificity remain underexplored. In this study, we conducted integrated proteomic and transcriptomic analyses of EVs derived from six dental stem cells (DSCs) and three systemic stem cells (SSCs) to investigate the role of EVs in tissue-specific molecular transfer. This study found that although DSCs and SSCs share 92.1% of the core proteome, the EVs derived from each stem cell type displayed distinct molecular signatures. EVs from DSCs were enriched in signaling molecules, reflecting their parent cells’ roles in local tissue repair, whereas EVs from SSCs carried mitochondrial and metabolic proteins, indicating their preferential involvement in metabolic regulation. Furthermore, we uncovered that the parent cells transferred 83% of the core proteins to their EVs in a tissue-specific pattern, ensuring that dental EVs retain prominent signaling functions. Thus, understanding the relationship between EVs and their parent stem cells with respect to tissue origin would be helpful to harness EVs as targeted therapeutic agents, particularly in oral regenerative medicine.
KW - dental stem cells
KW - extracellular vesicles
KW - lineage-specific protein transfer
KW - proteome
KW - systemic stem cells
KW - tissue origin
UR - https://www.scopus.com/pages/publications/105046923914
U2 - 10.1177/19373341261419438
DO - 10.1177/19373341261419438
M3 - 文章
C2 - 41742697
AN - SCOPUS:105046923914
SN - 1937-3341
JO - Tissue Engineering - Part A
JF - Tissue Engineering - Part A
ER -