TY - JOUR
T1 - Injectable hyaluronic acid-based microcapsules loaded with human endometrial stem cells improves cardiac function after myocardial infarction
AU - Salehi Namini, Mojdeh
AU - Khanmohammadi, Mehdi
AU - Beheshtizadeh, Nima
AU - Najafi, Mohammad Sadeq
AU - Heirani-Tabasi, Asieh
AU - Ayati, Aryan
AU - Boroumand, Safieh
AU - Pournemati, Behnam
AU - Ai, Jafar
AU - Ebrahimi-Barough, Somayeh
AU - Montazerghaem, Hossein
AU - Ahmadi Tafti, Seyed Hossein
N1 - Publisher Copyright:
© 2025
PY - 2025/4
Y1 - 2025/4
N2 - Therapeutic efficacy of human endometrial stem cells (hEnSCs) encapsulated in hyaluronic acid (HA)-based microcapsules for cardiac regeneration in a rat model of MI is investigated. Cell-enclosed microcapsules were made by loading hEnSCs within hydrogel membrane produced from modified HA possessing phenolic hydroxyl moieties (HA-Ph). The hEnSC-loaded HA-Ph microcapsules (≈150 μm) injected intramyocardially into the peri-infarct area post-MI. The encapsulated cells showed mechanical stability and >87 % cell viability with cellular aggregation in size of about 100 μm until 7 days of culture. Transthoracic echocardiography evaluation indicated a significant increase in ejection fraction in encapsulated cells, compared to the other groups. Histological investigation of fibrosis and scar area by Masson trichrome and hematoxylin and eosin (H&E) staining illustrated less fibrosis and scarring area in the encapsulated cell group compared with the other groups. Furthermore, the cell-laden microcapsules significantly enhance expression intensities of actin and troponin as well as vascular endothelial-specific marker, all of which promote cardiac functions and contribute to a better therapeutic effect than the free-cell injection group in a rat model of MI. Our findings demonstrated that both hEnSCs and specifically hEnSC-loaded HA-based hydrogel vehicle can provide a promising novel therapy for functional restoration in MI instances.
AB - Therapeutic efficacy of human endometrial stem cells (hEnSCs) encapsulated in hyaluronic acid (HA)-based microcapsules for cardiac regeneration in a rat model of MI is investigated. Cell-enclosed microcapsules were made by loading hEnSCs within hydrogel membrane produced from modified HA possessing phenolic hydroxyl moieties (HA-Ph). The hEnSC-loaded HA-Ph microcapsules (≈150 μm) injected intramyocardially into the peri-infarct area post-MI. The encapsulated cells showed mechanical stability and >87 % cell viability with cellular aggregation in size of about 100 μm until 7 days of culture. Transthoracic echocardiography evaluation indicated a significant increase in ejection fraction in encapsulated cells, compared to the other groups. Histological investigation of fibrosis and scar area by Masson trichrome and hematoxylin and eosin (H&E) staining illustrated less fibrosis and scarring area in the encapsulated cell group compared with the other groups. Furthermore, the cell-laden microcapsules significantly enhance expression intensities of actin and troponin as well as vascular endothelial-specific marker, all of which promote cardiac functions and contribute to a better therapeutic effect than the free-cell injection group in a rat model of MI. Our findings demonstrated that both hEnSCs and specifically hEnSC-loaded HA-based hydrogel vehicle can provide a promising novel therapy for functional restoration in MI instances.
KW - Cardiac regeneration
KW - Cell viability
KW - Endometrial stem cells
KW - Hyaluronic acid microcapsules
KW - Myocardial infarction (MI)
KW - Regenerative medicine
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UR - http://www.scopus.com/inward/citedby.url?scp=85217914607&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2025.140904
DO - 10.1016/j.ijbiomac.2025.140904
M3 - Article
C2 - 39938851
AN - SCOPUS:85217914607
SN - 0141-8130
VL - 304
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 140904
ER -