TY - JOUR
T1 - Establishment of salivary tissue-organoid biorepository
T2 - characterizing salivary gland stem/progenitor cells and novel differentiation marker PSMA/FOLH1
AU - Aalam, Syed Mohammed Musheer
AU - Varela, Ana Rita
AU - Khaderi, Aalim
AU - Mondesir, Ronsard J
AU - Mun, Dong-Gi
AU - Ding, Andrew
AU - Lombaert, Isabelle M A
AU - Coppes, Rob P
AU - Emperumal, Chitra Priya
AU - Pandey, Akhilesh
AU - Janus, Jeffrey R
AU - Kannan, Nagarajan
N1 - © 2025. The Author(s).
PY - 2025/5/21
Y1 - 2025/5/21
N2 - The salivary gland (SG) is vital for oral function and overall health through secretion of saliva. However salivary dysfunction due to aging, medications, autoimmune disorders, and cancer treatments poses significant challenges. We established the first diverse and clinically annotated salivary regenerative biobank at Mayo Clinic to study salivary gland stem/progenitor cells (SGSPCs). Optimization of cell isolation and progenitor assays revealed SGSPCs enriched within the CD24/EpCAM/CD49f+ and PSMA- phenotypes of both submandibular and parotid glands, with clonal differentiation assays highlighting heterogeneity. Induction of PSMA/FOLH1 expression was associated with SGSPC differentiation. Using mass spectrometry-based single cell proteomics, we identified 2461 proteins in SGSPC-enriched cells, including co-expressed cytokeratins, expressed in rare salivary ductal basal cells. Additionally, PRDX, a unique class of peroxiredoxin peroxidases enriched in SGSPCs, demonstrated H 2O 2-dependent growth, suggesting a role in salivary homeostasis. These findings provide a foundation for SGSPC research and potential regenerative therapies for salivary gland dysfunction.
AB - The salivary gland (SG) is vital for oral function and overall health through secretion of saliva. However salivary dysfunction due to aging, medications, autoimmune disorders, and cancer treatments poses significant challenges. We established the first diverse and clinically annotated salivary regenerative biobank at Mayo Clinic to study salivary gland stem/progenitor cells (SGSPCs). Optimization of cell isolation and progenitor assays revealed SGSPCs enriched within the CD24/EpCAM/CD49f+ and PSMA- phenotypes of both submandibular and parotid glands, with clonal differentiation assays highlighting heterogeneity. Induction of PSMA/FOLH1 expression was associated with SGSPC differentiation. Using mass spectrometry-based single cell proteomics, we identified 2461 proteins in SGSPC-enriched cells, including co-expressed cytokeratins, expressed in rare salivary ductal basal cells. Additionally, PRDX, a unique class of peroxiredoxin peroxidases enriched in SGSPCs, demonstrated H 2O 2-dependent growth, suggesting a role in salivary homeostasis. These findings provide a foundation for SGSPC research and potential regenerative therapies for salivary gland dysfunction.
U2 - 10.1038/s41536-025-00410-5
DO - 10.1038/s41536-025-00410-5
M3 - Article
C2 - 40399315
SN - 2057-3995
VL - 10
JO - npj Regenerative Medicine
JF - npj Regenerative Medicine
M1 - 23
ER -