Literature DB >> 36267534

Conditioned-medium of stem cells from human exfoliated deciduous teeth prevent apoptosis of neural progenitors.

Masagus Zainuri1,2, Jan Purba3, Sri Wa Jusman4, Endang W Bachtiar5.   

Abstract

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.

Entities:  

Keywords:  ANOVA, analysis of variance; Apoptosis; BDNF, brain derived neurotrophic factor; CM, conditioned medium; CM-SHED, conditioned medium of stem cells from human exfoliated deciduous teeth; CREB, cyclic adenosine monophosphate-response element binding protein; ELISA, enzyme-linked immunosorbent assay; ERK, extracellular signal-regulated kinases; GABA, gamma-aminobutyric acid; GABAAR1, GABA A1 receptor; GAD, glutamic acid decarboxylase; GAPDH, glyceraldehyde-3-phospate dehydrogenase; Gamma-aminobutyric acid; ICER, inducible cAMP early repressor; JAK/STAT, Janus kinase/ signal transducer and activator of transcription; MAPK, mitogen activated protein kinase; NMDAR, N-methyl-d-aspartate receptor; Neural progenitor; Neuroregeneration; PI3K, phosphoinositide-3-kinase; PKC, protein kinase C; PSA-NCAM, polysialic acid neural cell adhesion molecule; SHED, stem cells from human exfoliated deciduous teeth; Secretome; Stem cells from human exfoliated deciduous teeth; TGF, transforming growth factor; TrkB, tropomyosin receptor kinase B; hADSCs, human adipose-derived stem cells; mRNA, messenger RNA; pCREB, phosphorylated cyclic adenosine monophosphate-response element binding protein

Year:  2022        PMID: 36267534      PMCID: PMC9577352          DOI: 10.1016/j.sdentj.2022.08.005

Source DB:  PubMed          Journal:  Saudi Dent J        ISSN: 1013-9052


  29 in total

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