Publikasi Scopus 2010 s/d 2022

Zainuri M., Purba J., WA Jusman S., Bachtiar E.W.
57202456136;57867918400;57868601700;6507328763;
Conditioned-medium of stem cells from human exfoliated deciduous teeth prevent apoptosis of neural progenitors
2022
Saudi Dental Journal
34
7
565
571
Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Center For Research and Development of Biomedical and Basic Health Technology, National Institute of Health Research and Development, Ministry of Health, Indonesia; Department of Neurology Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Department of Biochemistry & Molecular Biology, Universitas Indonesia, Jakarta, Indonesia; Department of Oral Biology, Faculty of Dentistry and Oral Sciences Research Center, Universitas Indonesia, Jakarta, Indonesia
Zainuri, M., Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia, Center For Research and Development of Biomedical and Basic Health Technology, National Institute of Health Research and Development, Ministry of Health, Indonesia; Purba, J., Department of Neurology Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; WA Jusman, S., Department of Biochemistry & Molecular Biology, Universitas Indonesia, Jakarta, Indonesia; Bachtiar, E.W., Department of Oral Biology, Faculty of Dentistry and Oral Sciences Research Center, Universitas Indonesia, Jakarta, Indonesia
Purpose: This study aimed to evaluate the neuroprotective ability of the conditioned medium of stem cells from human exfoliated deciduous teeth (CM-SHED) to prevent glutamate-induced apoptosis of neural progenitors. Materials and methods: Neural progenitors were isolated from two-day-old rat brains, and the conditioned medium was obtained from a mesenchymal stem cell SHED. Four groups were examined: neural progenitor cells cultured in neurobasal medium with (N + ) and without (N-) glutamate and glycine, and neural progenitor cells cultured in CM-SHED with (K + ) and without (K-) glutamate and glycine. Results: The expression of GABA A1 receptor (GABAAR1) messenger RNA (mRNA) in neural progenitor measured by real-time quantitative PCR. GABA contents were measured by enzyme-linked immunosorbent assay, whereas the apoptosis markers caspase-3 and 7-aminoactinomycin D were analysed with a Muse® cell analyzer. The viability of neural progenitor cells in the K + group (78.05 %) was higher than the control group N- (73.22 %) and lower in the N + group (68.90 %) than in the control group. The K + group showed the highest GABA content, which significantly differed from that in the other groups, whereas the lowest content was observed in the N + group. The expression level of GABAAR1 mRNA in the K + group was the highest compared to that in the other groups. CM-SHED potently protected the neural progenitors from apoptosis. Conclusions: CM-SHED may effectively prevent glutamate-induced apoptosis of neural progenitors. © 2022 The Author
Apoptosis; Gamma-aminobutyric acid; Neural progenitor; Neuroregeneration; Secretome; Stem cells from human exfoliated deciduous teeth
4 aminobutyric acid; 4 aminobutyric acid A receptor; 7 aminodactinomycin; caspase 3; glycine; messenger RNA; nerve cell adhesion molecule; polysialic acid; animal cell; animal tissue; apoptosis; Article; cell therapy; cell viability; controlled study; deciduous tooth; degenerative disease; enzyme linked immunosorbent assay; flow cytometry; mesenchymal stem cell; mRNA expression level; neural stem cell; neuroprotection; nonhuman; phenotype; protein expression; protein expression level; rat; real time polymerase chain reaction; stem cell culture
District of Columbia Developmental Center for AIDS Research; Ministry of Health
MZ was supported by a grant from the Center for Research and Development of Biomedical and Basic Health Technology, National Institute of Health Research and Development, Ministry of Health, Republic of Indonesia. EWB was Partly supported by NKB-816/UN2.RST/HKP.05.00/2022.
Elsevier B.V.
10139052
Article
Q2
490
10199