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Stem cell-derived exosomes from human exfoliated deciduous teeth promote angiogenesis in hyperglycemic-induced human umbilical vein endothelial cells
SUNARTVANICHKUL, Thanapat; ARAYAPISIT, Tawepong; SANGKHAMANEE, Sujiwan Seubbuk; CHAWEEWANNAKORN, Chaiyapol; IWASAKI, Kengo; KLAIHMON, Phatchanat; SRITANAUDOMCHAI, Hathaitip.
  • SUNARTVANICHKUL, Thanapat; Mahidol University. Faculty of Dentistry. Department of Orthodontics. Bangkok. TH
  • ARAYAPISIT, Tawepong; Mahidol University. Faculty of Dentistry. Department of Anatomy. Bangkok. TH
  • SANGKHAMANEE, Sujiwan Seubbuk; Mahidol University. Faculty of Dentistry. Department of Oral Medicine and Periodontology. TH
  • CHAWEEWANNAKORN, Chaiyapol; Mahidol University. Faculty of Dentistry. Department of Orthodontics. Bangkok. TH
  • IWASAKI, Kengo; Osaka Dental University. Advanced Medical Research Center, Translational Research Institute for Medical Innovation. Osaka. JP
  • KLAIHMON, Phatchanat; Mahidol University. Faculty of Medicine Siriraj Hospital. Siriraj Center of Excellence for Stem Cell Research. Bangkok. TH
  • SRITANAUDOMCHAI, Hathaitip; Mahidol University. Faculty of Dentistry. Department of Oral Biology. Bangkok. TH
J. appl. oral sci ; 31: e20220427, 2023. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1430628
ABSTRACT
Abstract Objective To investigate the angiogenesis in human umbilical vein endothelial cells (HUVEC) under high glucose concentration, treated with exosomes derived from stem cells from human exfoliated deciduous teeth (SHED). Methodology SHED-derived exosomes were isolated by differential centrifugation and were characterized by nanoparticle tracking analysis, transmission electron microscopy, and flow cytometric assays. We conducted in vitro experiments to examine the angiogenesis in HUVEC under high glucose concentration. Cell Counting Kit-8, migration assay, tube formation assay, quantitative real-time PCR, and immunostaining were performed to study the role of SHED-derived exosomes in cell proliferation, migration, and angiogenic activities. Results The characterization confirmed SHED-derived exosomes size ranged from 60-150 nm with a mode of 134 nm, cup-shaped morphology, and stained positively for CD9, CD63, and CD81. SHED-exosome significantly enhanced the proliferation and migration of high glucose-treated HUVEC. A significant reduction was observed in tube formation and a weak CD31 staining compared to the untreated-hyperglycemic-induced group. Interestingly, exosome treatment improved tube formation qualitatively and demonstrated a significant increase in tube formation in the covered area, total branching points, total tube length, and total loop parameters. Moreover, SHED-exosome upregulates angiogenesis-related factors, including the GATA2 gene and CD31 protein. Conclusions Our data suggest that the use of SHED-derived exosomes potentially increases angiogenesis in HUVEC under hyperglycemic conditions, which includes increased cell proliferation, migration, tubular structures formation, GATA2 gene, and CD31 protein expression. SHED-exosome usage may provide a new treatment strategy for periodontal patients with diabetes mellitus.


Full text: Available Index: LILACS (Americas) Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2023 Type: Article Affiliation country: Japan / Thailand Institution/Affiliation country: Mahidol University/TH / Osaka Dental University/JP

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Full text: Available Index: LILACS (Americas) Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2023 Type: Article Affiliation country: Japan / Thailand Institution/Affiliation country: Mahidol University/TH / Osaka Dental University/JP